Trabajos Science en New Jersey

Job Description Position Purpose: The primary purpose of this position is to serve as the lead synthetic chemist at the Transportation Security Laboratory (TSL). Essential Duties and Responsibilities: • Follows currently established standard operating procedures (SOPs) to synthesize homemade explosives (HMEs)., • Performs research to develop syntheses for new HMEs of interest., • Performs quality control of HMEs synthesized at the TSL., • Works directly with federal client to achieve the goals of the HME laboratory at the TSL., • Performs wet chemistry (dilutions, extractions, etc.)., • Composes and reviews technical reports and SOPs., • Composes, reviews, and executes test plans., • Performs literature reviews., • Safely handles explosive and other hazardous materials., • Sources materials and submits purchase requests., • Other duties as assigned. Required Knowledge, Skills & Abilities: • Previous experience synthesizing and handling energetic material., • Good interpersonal, verbal, and written communication skills., • Good listening skills., • Team player with a positive attitude., • Good working skills of software and tools necessary for job functions including Microsoft Office suite., • Experience with measuring density and refractive index, • Experience with IR, RAMAN, or NMR, • Experience with using EasyMax for chemical syntheses Education/Experience: Incumbent professional should have: a bachelor's degree in chemistry with a minimum of five years relevant experience; or a master's degree in chemistry with at least two years of relevant experience; or a PhD in Chemistry with at least one year of relevant experience. Certificates and Licenses: None Clearance: The ability to obtain a Secret clearance and Department of Homeland Security suitability is required for this position. Supervisory Responsibilities: The incumbent professional may oversee junior level chemists performing synthetic chemistry tasks. Working Conditions/ Equipment: The incumbent professional is expected to work and/or be available during regular business hours. He/she should also generally be available via e-mail or phone during non-business hours as needed to address critical issues or emergencies. He/she may be required to travel on behalf of the company up to 25%. The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions and perform any other related duties, as assigned by their supervisor.

Job Description Position Purpose: The purpose of this position is to provide analytical chemistry subject matter expertise to one or more chemistry-based applied research projects. Essential Duties and Responsibilities: • Develops and validates analytical methods using thermal desorption (TD), gas chromatography (GC), liquid chromatography (LC), ion chromatography (IC), mass spectrometry (MS), and microscopy., • Performs troubleshooting and non-routine maintenance on TD, GC, LC, IC, MS, and microscopy instrumentation., • Ensures the readiness of TD, GC, LC, IC, MS, and microscopy instrumentation, • Facilitates the stand-up of new analytical instrumentation, • Leads meetings with company clients by preparing and presenting meeting materials in meetings, • Develops innovative solutions to complex problems, • Develops improvements to currently used processes and analysis methods, • Trains, leads, and mentors junior level scientists to execute analytical chemistry tasks, • Performs wet chemistry (dilutions, extractions, etc.), • Composes, reviews, and executes test plans and standard operating procedures, • Composes and reviews technical reports, • Performs literature reviews, • Safely handles explosives and other hazardous materials, • Sources materials and submits purchase requests, • Other duties as assigned Required Knowledge, Skills & Abilities: • Positive attitude with a willingness to learn new things, • Previous experience with TD, GC, LC, IC, or MS, • Excellent working knowledge of TD, GC, LC, IC, and MS, • Technical writing, presentation, verbal communication, and listening skills Education/Experience: Incumbent professional should have a minimum of a bachelor's degree in chemistry with five to ten years of analytical chemistry experience or a graduate degree (masters or PhD) chemistry with up to five years of experience. Certificates and Licenses: None Clearance: The ability to obtain a Secret clearance and Department of Homeland Security suitability is required for this position. Supervisory Responsibilities: The incumbent professional has little to no supervisory responsibilities. Working Conditions/ Equipment: The incumbent professional is expected to work and/or be available during regular business hours. He/she should also generally be available via e-mail or phone during non-business hours as needed to address critical issues or emergencies. He/she may be required to travel on behalf of the company up to 25%. The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions and perform any other related duties, as assigned by their supervisor.

Job Description Position Purpose: We are seeking a skilled Thermal Chemist to conduct advanced thermal analysis and materials characterization in support of chemical formulation and materials development programs. This role requires strong knowledge of industrial chemical processes, thermal analysis techniques, and sophisticated analytical methods. The successful candidate will play a critical role in developing, testing, and characterizing chemical formulations while ensuring the highest standards of safety and analytical excellence. Essential Duties and Responsibilities: • Advanced Thermal Analysis:, • Conduct detailed thermal analysis of materials using differential scanning calorimetry (DSC), • Perform thermogravimetric analysis (TGA) to assess decomposition pathways and thermal stability, • Operate accelerating rate calorimetry (ARC) systems for comprehensive thermal hazard evaluation, • Analyze kinetic parameters and reaction mechanisms of material decomposition, • Develop thermal models and predictive capabilities for safety and performance assessment, • Data Analysis & Reporting:, • Analyze complex thermal and analytical data to extract meaningful insights about material properties, • Prepare comprehensive technical reports documenting experimental results and conclusions, • Present findings to technical teams, management, and external stakeholders, • Maintain detailed laboratory notebooks and ensure data integrity and traceability, • Support patent applications and technical publications, • Materials Characterization & Analysis:, • Perform comprehensive materials characterization using vibrational spectroscopy techniques (FTIR, Raman), • Conduct particle size analysis to determine morphology and distribution characteristics, • Execute sensitivity testing protocols including electrostatic discharge (ESD), friction, and impact sensitivity assessments, • Analyze chemical composition, purity, and stability of energetic materials and intermediates, • Required Knowledge, Skills & Abilities:, • Advanced knowledge of chemical thermodynamics and materials science principles, • Proficiency with thermal analysis software and data interpretation, • Experience with statistical analysis and experimental design, • Understanding of chemical reaction mechanisms and kinetic modeling Education/Experience A bachelor’s degree in chemistry with at least 12 years of experience OR a master’s degree in chemistry with at least 6 years of experience OR a Ph.D. in chemistry with at least 1 year of experience. Certificates & Licenses: None Required Clearance: The ability to obtain a Department of Defense Secret clearance and Department of Homeland Security Fitness is required for this position. Supervisory Responsibilities: Supervision of the technical activities performed by the more junior staff members assigned to the project is required for this position. Working Conditions/Equipment: The incumbent professional is expected to be present at the work site and/or be available during regular business hours. He/she should also generally be available via e-mail or phone during non-business hours as needed to address critical issues or emergencies. The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties, as assigned by their supervisor.

Job Description Position Purpose: The primary purpose of this position is to perform chemistry tasks at the Transportation Security Laboratory (TSL). Essential Duties and Responsibilities: • Collects and analyzes data using gas chromatography (GC), liquid chromatography with mass spectrometry detection (LCMS), and ion chromatography (IC)., • Performs troubleshooting, maintenance, and method development on GC, LCMS, and IC instrumentation., • Performs wet chemistry (dilutions, extractions, etc.)., • Collects and analyzes data using explosive trace detection (ETD) systems., • Performs microscopy measurements using stereomicroscope or polarized light microscope., • Composes and reviews technical reports and standard operating procedures., • Composes, reviews, and executes test plans., • Synthesizes homemade explosives., • Performs literature reviews., • Safely handles explosive and other hazardous materials., • Sources materials and submits purchase requests., • Other duties as assigned. Required Knowledge, Skills & Abilities: • Positive attitude., • Good working knowledge of trace analytical instrumentation (GC, LCMS, and IC)., • Good interpersonal, verbal, and written communication skills., • Good listening skills., • Good working skills of software and tools necessary for job functions including Microsoft Office suite., • Previous experience handling energetic material., • Previous experience with ETD systems. Education/Experience: Incumbent professional should have a minimum of a bachelor's degree in chemistry. Certificates and Licenses: None Clearance: The ability to obtain a Secret clearance and Department of Homeland Security suitability is required for this position. Supervisory Responsibilities: The incumbent professional has little to no supervisory responsibilities. Working Conditions/ Equipment: The incumbent professional is expected to work and/or be available during regular business hours. He/she should also generally be available via e-mail or phone during non-business hours as needed to address critical issues or emergencies. He/she may be required to travel on behalf of the company up to 25%. The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions and perform any other related duties, as assigned by their supervisor.

Job DescriptionCompany Description With more than 100 years of experience, Sika is a worldwide innovation and sustainability leader in the development and production of systems and products for commercial and residential construction, as well as the transportation, marine, automotive, and renewable energy manufacturing industries. Sika is a specialty chemicals company with a globally leading position in the development and production of systems and products for bonding, sealing, damping, reinforcing, and protection in the building sector and industry. Sika has subsidiaries in 103 countries around the world, produces in over 400 factories, and develops innovative technologies for customers worldwide. In doing so, it plays a crucial role in enabling the transformation of the construction and transportation industries toward greater environmental compatibility. Approximately 33,000 employees generated CHF 11.20 billion in sales in 2025. Job Description Sika is looking for an experienced Jr. Chemist to join its growing team in Lyndhurst, NJ. With an innovative mind for new concepts and chemistry, laboratory benchwork contributes to the development of new technology platforms for new products. Conduct basic research into chemistry that is relevant to sealants and adhesives and their applications. Develop new products. Provide technical support to production plants and customers. Specific Responsibilities: • Execute feasibility studies and project designs on the bench to generate meaningful data for project progression, • Be organized, have a strong attention to detail, and effectively multitask projects., • Test products according to Industry standards and Sika Procedures to ensure product quality and performance., • Participate in implementing new products/technologies to Sika factories., • Perform initial material testing and gain material approvals from customers., • Initiate and attend technical presentations from raw material suppliers., • Keep accurate records and maintain good laboratory & QC notebook practice., • Visit customer sites and provide technical solutions to customers., • Work with internal customers: sales, marketing, EHS, and production in assigned activities, • Participate in and contribute to TC Lyndhurst Safety, Nuage and 5S activities and interact with other Sika global platforms., • Maintain a safe, tidy and harassment free work environment., • Provide accurate and detailed reports using good data collection and analytic skills., • Maintain assigned equipment in good operating condition., • Attend all necessary training requested by the company, • Learn and follow Sika processes such as PDP, Monthly Reporting Contribution, …, • Strong teamwork and work in various team environments., • Must be able to travel, approx. 10% of work time Qualifications Qualifications/Experience/Education: • BS degree, preferably in Chemistry, Polymer Science, or Chemical Engineering; will also be considered., • 0-2 years of hands-on industrial laboratory experience. Experience in sealants and adhesives preferred., • Design of Experiments (DOE) experience preferred but not required., • Strong presentation skills. Excellent technical and business writing skills. Good computer skills in Microsoft Word, Excel, PowerPoint, and Project Management Additional Information • 401k with Generous Company Match, • Bonuses, • Medical, Dental, and Vision Benefits, • Paid Parental Leave, • Life Insurance, • Disability Insurance, • Paid time off, paid holidays, • Floating holidays + Paid Volunteer Time, • Wellness/Fitness Reimbursements, • Education Assistance, • Professional Development Opportunities, • Employee Referral Program & More! Sika fosters a culture of entrepreneurship, empowering each individual to make decisions, learn from experiences, and shape their own career path. The safety and well-being of employees are top priorities at Sika, with a strong commitment to open communication and maintaining a safe workplace. In addition, Sika actively contributes to the community and promotes sustainability by giving back, minimizing environmental impact, and embracing social responsibility. We offer competitive salaries, aligned with local market benchmarks and the specific scope and responsibilities of each role. Compensation is determined based skills relevant to the position, education and/or training. We are committed to fair and equitable pay practices in accordance with applicable laws and regulations. Sika Corporation is committed to a work environment that supports, inspires, and respects all individuals that apply. As an equal opportunity employer Sika will consider all qualified applicants without discrimination on the basis of race, color, religion, sex, pregnancy, sexual orientation, gender identity, age, disability, national or ethnic origin, or other protected characteristics. We offer competitive salaries, aligned with local market benchmarks and the specific scope and responsibilities of each role. Compensation is determined based skills relevant to the position, education and/or training. We are committed to fair and equitable pay practices in accordance with applicable laws and regulations.

Job Description Job Description Date 02/2024 Location 1300 Airport Road, North Brunswick NJ Title Lead, Quality Control Chemist Department Quality Control Reports to Manager, Quality Control Laboratory FLSA (Exempt or Non-Exempt Exempt Role Overview The Lead, QC Chemist performs specific routine analysis of samples of raw materials, in process, and finished products according to established (official and/or in-house) test procedures. Testing assesses the strength, identify, purity of the test samples and/or raw materials. The Chemist prepares reagents, standards, and solutions and may monitor and verify quality in accordance with statistical process and other control procedures. The Chemist maintains & organizes testing’s and compliance while working in a fast-paced environment with changing priorities. The duties and responsibilities described for each level are not limited to those outlined and are not intended to be a comprehensive list of all activities, functions, or responsibilities required of the position. Management reserves the right to modify, assign, or reassign duties and responsibilities at any time based on business needs. Areas of Responsibility • Performs assigned sampling, physical, chemical tests and assay on raw materials, active dietary ingredients, in-process, finished, and stability products in an FDA regulated lab environment. Uses a variety of wet chemicals, physical and instrumental techniques as well as routine QC instruments HPLC, GC, IR, Auto Titrator, Bulk Density, UV Spectrophotometer, Dissolution, Karl Fisher (KF), Potentiometer., • Troubleshoots HPLC, GC, QC instruments for specific tests in order to assist in determining the root cause of aberrant results and help in performing Lab investigations / OOS., • Evaluates daily raw data sheets for product samples and release, if needed., • Coordinates annual review of STPS / SOPS as per USPL procedures., • Prepare new methods and test procedures for new or existing raw materials and finished products., • Ensures compliance with company and customer specifications as well as federal, state and local regulatory requirements., • Perform floor supervision of QC Chemists for routine testing, if required., • Prepares and reviews QC related documents during and finishing of testing of sample. Submit all testing related documents like data sheets, chromatograms, spectras, instruments print outs in timely manner to Qc Documentation department to release the batch of raw material / finished product., • Prepares and/or Reviews Test Procedures, SOP's and Protocols as assigned., • Performs maintenance and calibrations of laboratory instruments /equipment, if required to help in-house calibrations., • Assures GMP compliance according to FDA CFR Part 111 and USPL SOPs / guidelines., • Complies with all regulatory/ in-house requirements (may include but not be limited to safety, housekeeping, laboratory chemical waste, cGMP, GLP, documentation) when performing the assigned activity., • Trains new QC Chemists to perform instrumental testing., • Must be able to work extended hours as needed and occasional weekends., • Other duties and responsibilities as assigned by QC in-charge / management. Other Responsibilities Including Safety: • Works in a safe and responsible manner to create an injury-free and incident-free workplace., • Complies with all job-related safety and other training requirements., • Keeps management informed of area activities and of any significant problems. Requirements Education & Qualification: • BS/MS in Chemistry or related scientific disciplines., • Five (5) years of basic chemistry techniques (can be academic) is a plus., • Minimum of 5 years QC lab work experience in handling HPLC, GC, KF, Dissolution, DT and other sophisticated lab instruments in dietary supplements, food or OTC / Pharmaceutical manufacturing industry. Certifications, Licenses, Credentials: • N/A Skills & Ability • Ability to maintain integrity and honesty at all times and to communicate with transparency., • Ability to work independently or as part of a team., • Solid understanding of cGMP’s and GLP and is familiar with 21 CFR Part 11., • Strong working knowledge of Microsoft Word, Excel., • Good documentation practices and able to write simple, clear reports., • Meets commitments on time and practices time-management skills., • Seeks to identify continuous improvement needs., • Experience with Shimadzu LC2010, Nexera, GC2010, Thermo ICP-MS, Labsolution and Waters, • Empower Lab Software a plus. Physical Requirements (lifting, etc.): • Ability to navigate office, lab, and/or plant floor working environments., • Uses hands to finger, handle, feel, or operate objects or controls, lifting to waist height and/or above shoulder height, frequent bending from the waist, or squatting, walking short distances and leaning over equipment as well as kneeling on the floor to clean under the equipment., • Must be able to wear all PPE including a lab coat, face mask, booties, gloves, safety glasses/goggles, and respirators., • On occasion may need to lift up to 20lbs Work Environment (Office, Warehouse, temperature extremes, etc.): • Work is regularly performed inside a laboratory environment where temperatures can be moderate, exposure to dust, odors, noise, and fumes. The noise level is usually moderate. Employees can be exposed daily to chemicals and cleaning agents., • May execute up to 20% of their work at the bench level either standing or sitting on a stool., • Work performed in a standard office environment is without unpleasant or hazardous conditions. The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all the job responsibilities, duties, skill, or working conditions. In addition, this document does not create an employment contract, implied or otherwise, other than an "at will" relationship. USPL is proud to be an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, age, genetic information, disability, protected veteran status, or any other characteristic protected by applicable local, state, or federal law. Benefits And Compensation: Our benefits are designed to help you move forward in your career, and in areas of your life outside of USPL. From health and wellness benefit options including: medical, dental, vision, short and long term disability, basic life insurance, supplemental life insurance, AD&D insurance. We also offer a matched 401(k) savings plan. Employees have the opportunity to receive compensation in the form of premium pay such as overtime, shift differential, holiday pay, sick time, etc. Newly hired employees receive up to 10 days of vacation the first year, which grows to 12 days starting the second year of employment. Job Description Acknowledgement I have read and understand the job requirements, responsibilities, and expectations set forth in the job description provided for my position. I attest that I can perform the essential job functions as outlined with or without any reasonable accommodation.

Job DescriptionCompany Description With more than 100 years of experience, Sika is a worldwide innovation and sustainability leader in the development and production of systems and products for commercial and residential construction, as well as the transportation, marine, automotive, and renewable energy manufacturing industries. Sika is a specialty chemicals company with a globally leading position in the development and production of systems and products for bonding, sealing, damping, reinforcing, and protection in the building sector and industry. Sika has subsidiaries in 103 countries around the world, produces in over 400 factories, and develops innovative technologies for customers worldwide. In doing so, it plays a crucial role in enabling the transformation of the construction and transportation industries toward greater environmental compatibility. Approximately 33,000 employees generated CHF 11.20 billion in sales in 2025. Job Description Broad Function and Purpose of Position: Sika is looking for an experienced Chemist to join its growing team in Lyndhurst, NJ. With an innovative mind for new concepts and chemistry, laboratory benchwork contributes to the development of new technology platforms for new products. Responsible for maintaining existing products and developing new ones, and for providing technical support to production plants and customers. Specific Responsibilities: • Responsible for managing assigned projects (from Idea Proposal to Product Release), • Independently develop new products according to customer specifications., • Develop DOE and Design FEMA for product development., • Participate in 3-year or long-term product/technology planning, • Evaluate new testing instruments and make recommendations for capital expenditures., • Define new product QA requirements to ensure product quality and performance., • Responsible for transferring new products/technologies to the Processing group., • Perform initial material testing and gain material approvals from customers., • Provide technical support to the manufacturing plant to ensure product quality., • Support internal procedures, PCP, and ISO processes., • Keep accurate records and maintain good laboratory notebook practice., • Publish Research Proposals, Field Trial Proposals and Product Releases as required., • Publish progress reports, trip reports and monthlies on approved projects., • Visit customer sites and provide technical solutions to customers., • Initiate and attend technical presentations from raw material suppliers., • Maintain a safe, tidy, and harassment free work environment, • Maintain assigned equipment in good operating condition., • Provide training to new employees, technicians or Junior Chemists. Qualifications Qualifications/Experience/Education: • BS or MS or Ph.D degree in Chemistry, Polymer Science or Chemical Engineering or equivalent., • 2+ year’s hand-on industrial experience in cement chemistry or cementitious based formaultions, • Good oral communication, technical presentation and technical writing skills, • Good skills in Excel, Word and PowerPoint or equivalent., • Experience in Design of Experiments, Design FMEA and other quality programs is a plus Additional Information Perks & Benefits • 401k with Generous Company Match, • Bonuses, • Medical, Dental, and Vision Benefits, • Paid Parental Leave, • Life Insurance, • Disability Insurance, • Paid time off, paid holidays, • Floating holidays + Paid Volunteer Time, • Wellness/Fitness Reimbursements, • Education Assistance, • Professional Development Opportunities, • Employee Referral Program & More! Sika fosters a culture of entrepreneurship, empowering each individual to make decisions, learn from experiences, and shape their own career path. The safety and well-being of employees are top priorities at Sika, with a strong commitment to open communication and maintaining a safe workplace. In addition, Sika actively contributes to the community and promotes sustainability by giving back, minimizing environmental impact, and embracing social responsibility Sika Corporation is committed to a work environment that supports, inspires, and respects all individuals that apply. As an equal opportunity employer Sika will consider all qualified applicants without discrimination on the basis of race, color, religion, sex, pregnancy, sexual orientation, gender identity, age, disability, national or ethnic origin, or other protected characteristics. We offer competitive salaries, aligned with local market benchmarks and the specific scope and responsibilities of each role. Compensation is determined based skills relevant to the position, education and/or training. We are committed to fair and equitable pay practices in accordance with applicable laws and regulations.

Job Description Job Title: QC Chemist (cGMP / HPLC / Solid Dose) Location: Cranbury, NJ (Onsite) Type: Contract-to-Hire Schedule: 40 hrs/week Shift: M-F 8am-5pm Pay: $36-40/hour depending upon experience Overview Seeking an experienced QC Chemist / Quality Control Analyst to support batch release, stability testing, and analytical testing in a cGMP pharmaceutical manufacturing environment. Ideal candidates will have strong experience with solid oral dosage forms (tablets/capsules) and hands-on HPLC/UPLC analysis. Key Responsibilities • Perform batch release and stability testing for pharmaceutical products, • Conduct assay, dissolution, impurity, and related substances testing, • Operate, calibrate, and troubleshoot HPLC / UPLC systems, • Maintain GMP documentation and ensure audit readiness (ALCOA+), • Investigate OOS / OOT results and support CAPA activities, • Manage stability programs, sample pulls, and trending analysis, • Collaborate with QA and Manufacturing to meet production timelines Requirements • 6–8+ years of pharmaceutical QC experience (cGMP REQUIRED), • Strong background in solid oral dosage (tablets, capsules), • Recent hands-on experience with HPLC / UPLC (REQUIRED), • Experience with assay, dissolution, impurities, and stability testing, • Working knowledge of FDA, GMP, ICH guidelines, • Experience with Empower, LIMS, or similar systems, • Strong documentation, data integrity (ALCOA+), and troubleshooting skills, • Ability to work independently and in a fast-paced manufacturing setting Keyskills QC Chemist, Quality Control Analyst, cGMP, GMP, Pharmaceutical, Solid Dose, Solid Oral Dosage, Tablets, Capsules, HPLC, UPLC, Dissolution, Assay, Impurities, Stability Testing, Batch Release, OOS, OOT, CAPA, FDA, ICH, Empower, LIMS, Analytical Chemistry, Drug Product, Manufacturing, Validation Benefits (via System One) Medical, Dental, Vision, 401(k), Life Insurance, and additional voluntary benefits System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. #M3- #LI- Ref: #558-Scientific

Job DescriptionTitle: Sr. Chemist - Skincare/Color Reports to: Chief Scientific Officer Department: R&D – Skincare Responsibility Summary: The Sr. Chemist is responsible for leading the development of innovative skincare formulations while supporting business and client needs. This role oversees product development from concept through scale-up, ensures compliance with regulatory requirements (including OTC and color), and provides technical leadership by mentoring junior chemists. The position also involves collaboration with cross-functional teams and customers, evaluation of new materials and technologies, and support within both laboratory and production environments to ensure high-quality, market-ready products. Responsibilities: The Sr. Chemist is responsible for supporting the company's business events through a variety of tasks, including: • Formulate and facilitate development of innovative skin care products, line extensions, and product improvements., • Supervise, mentor, teach, and lead junior chemists in skincare cosmetics formulation., • Proactively scan and research new concepts, materials, technical opportunities and partnerships., • Work in the production environment whenever necessary., • Work with project managers/customers to develop the product forms and shade palettes they expect., • Understand and comply with color regulations., • Developing stability protocols for skincare products and monitor product stability., • Advise on lab equipment needs., • Perform other duties as assigned by manager. Qualifications:, • BS in Chemistry or higher in a related field., • Minimum of 8 years in developing R&D skin care formulations., • Must have experience in OTC product development., • SPF and color formulation experience is preferred., • Strong understanding of formulations and scale-up., • Have good understanding of production equipment and their uses., • Have a good understanding of the raw materials used in skincare cosmetics., • Ability to lift and carry up to 10-15 pounds.Compensation & Benefits: The approximate pay range for this position is $80,000 - $110,000. Final compensation may vary based on factors including but not limited to knowledge, skills and abilities. The benefit package includes: • Medical, Dental, Vision, Life, • PTO, • Special Paid Leave for employees’ personal events, • Company Paid Holidays, • 401(k) employer match, • Year-End G Powered by JazzHR 0hzau6GAfk

Job Description Date 06/2020 Location 1200 Airport Road, North Brunswick NJ Title Chemist, Quality Control 3 Department Quality Control Reports to Manager, Chemistry Laboratory FLSA (Exempt or Non-Exempt Exempt Role Overview The Chemist, QC 3 performs specific routine analysis of samples of raw materials, in process, and finished products according to established (official and/or in-house) test procedures. Testing assesses the strength, identify, purity of the test samples and/or raw materials. The Chemist prepares reagents, standards, and solutions and may monitor and verify quality in accordance with statistical process and other control procedures. The Chemist maintains organization and compliance while working in a fast-paced environment with changing priorities. The duties and responsibilities described for each level are not limited to those outlined and are not intended to be a comprehensive list of all activities, functions, or responsibilities required of the position. Management reserves the right to modify, assign, or reassign duties and responsibilities at any time based on business needs. Areas of Responsibility • Troubleshoot /test specific batches in order to assist in determining the root cause of off-spec product and makes recommendations for ingredient adjustments to meet required specifications., • Ensures compliance with company and customer specifications as well as federal, state and local regulatory requirements, • Investigates customer complaints and provides management with test results information., • Performs assigned sampling, physical, chemical tests and assay on raw materials, active pharmaceutical ingredients, in-process, finished, and stability products in an FDA regulated lab environment. Uses a variety of wet chemicals, physical and instrumental techniques as well as routine QC instruments (HPLC, GC, IR, Auto Titrator, Bulk Density, UV Spectrophotometer, Dissolution, Karl Fisher (KF), Potentiometer)., • Performs complicated testing with supervisory direction. Documents work clearly and performs tests accurately., • Preparation and review of QC related documents is 5%of daily activities., • Test of samples/raws as assigned and reports the results. Testing activities represents 95% of daily work., • Prepares and/or Reviews Test Procedures, SOP's and Protocols as assigned., • Performs maintenance and calibrations of laboratory instruments /equipment with supervisory direction/training., • Complies with all regulatory/ in-house requirements (may include but not be limited to safety, housekeeping, laboratory chemical waste, cGMP,GLP, documentation) when performing the assigned activity., • Must be able to work extended hours as needed and occasional weekends., • Other duties and responsibilities as assigned. Other Responsibilities Including Safety: • Works in a safe and responsible manner to create an injury-free and incident-free workplace., • Complies with all job-related safety and other training requirements., • Keeps management informed of area activities and of any significant problems. Requirements Education & Qualification: • BS in Chemistry or related scientific disciplines, • One (1) year of basic chemistry techniques (can be academic) is a plus, • Minimum of 1 -3 years QC lab work experience with industry experience in dietary supplements, food, or OTC manufacturing. Certifications, Licenses, Credentials: • N/A Skills & Ability • Ability to maintain integrity and honesty at all times and to communicate with transparency., • Ability to work independently or as part of a team., • Solid understanding of cGMP’s and GLP and is familiar with 21 CFR Part 11, • Strong working knowledge of Microsoft Word, Excel., • Good documentation practices and able to write simple, clear reports, • Meets commitments on time and practices time-management skills, • Seeks to identify continuous improvement needs, • Experience with Shimadzu LC2010, Nexera, GC2010, Thermo ICP-MS, Labsolution and Waters Empower Lab Software a plus. Physical Requirements (lifting, etc.): • May execute 90%-100% of their work at the bench level either standing or sitting on a stool., • Uses hands to finger, handle, feel, or operate objects or controls, lifting to waist height and/or above shoulder height, frequent bending from the waist, or squatting, walking short distances and leaning over equipment as well as kneeling on the floor to clean under the equipment., • Must be able to wear all PPE including a lab coat, face mask, booties, gloves, safety glasses/goggles, and respirators., • On occasion may need to lift up to 35 lbs., • Ability to navigate office, lab, and/or plant floor working environments. Work Environment (Office, Warehouse, temperature extremes, etc.): • Approximately 80% of work performed in a laboratory environment which may have unpleasant odors or hazardous conditions., • Temperatures can be moderate, exposure to dust, odors, noise, and fumes. The noise level is usually moderate. Employees can be exposed daily to chemicals and cleaning agents. The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all the job responsibilities, duties, skill, or working conditions. In addition, this document does not create an employment contract, implied or otherwise, other than an “at will” relationship. USPL is proud to be an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, age, genetic information, disability, protected veteran status, or any other characteristic protected by applicable local, state, or federal law. Benefits And Compensation: Our benefits are designed to help you move forward in your career, and in areas of your life outside of USPL. From health and wellness benefit options including: medical, dental, vision, short and long term disability, basic life insurance, supplemental life insurance, AD&D insurance. We also offer a matched 401(k) savings plan. Employees have the opportunity to receive compensation in the form of premium pay such as overtime, shift differential, holiday pay, sick time, etc. Newly hired employees receive up to 10 days of vacation the first year, which grows to 12 days starting the second year of employment. Job Description Acknowledgement I have read and understand the job requirements, responsibilities, and expectations set forth in the job description provided for my position. I attest that I can perform the essential job functions as outlined with or without any reasonable accommodations.

Job DescriptionTitle: Chemist Reports to: Director of Color & Innovation Department: R&D - Color Responsibility Summary: The Chemist will be responsible for analyzing batches, measuring physical parameters such as Viscosity, pH, and Density, interacting with vendors, documenting, collaborating with supervisor, and entering formulation. Responsibilities: The Chemist is responsible for supporting the company's business events through a variety of tasks, including: • Maintain a lab note book., • Make batches., • Create ingredient qualitative and quantitative list., • Check next day specification from previous day batch., • Follow up with on-going stabilities., • Communicate with raw material vendors., • Attend in-house vendor presentations., • Enter formulation into the company formulator., • Review results with supervisor., • Analyze lab batch measuring physical parameters: Viscosity, pH, and Density., • Assist in the formulation and development of innovative skin care and color cosmetic products, including line extensions and product improvements., • Support in color matching and formulation adjustments., • Support compliance with color regulations and internal quality standards., • Maintain laboratory equipment and ensure proper organization of raw materials and samples. Qualifications: • Bachelor’s degree in Chemistry (or Biology that has had chemistry and organic chemistry classes)., • 2- 5 years of experience in R&D, formulation, emulsions, and other forms of color product formulations., • Well organized and highly detail oriented., • Must work well with others and communicate effectively., • Strong understanding of cosmetic raw materials, formulation principles, production equipment., • Strong color matching skills., • Ability to lift and carry up to 10-15 pounds. Compensation & Benefits: The approximate pay range for this position is $60,000 - $68,000. Final compensation may vary based on factors including but not limited to knowledge, skills and abilities. The benefit package includes: • Medical, Dental, Vision, • Life/AD&D Insurance, • Paid Time Off (PTO), • Special Paid Leave for employees’ personal events, • Company Paid Holidays, • 401(k) with employer match, • Year-End Gift Powered by JazzHR As9zTT4HPe

Job DescriptionCoreWeave is The Essential Cloud for AI™. Built for pioneers by pioneers, CoreWeave delivers a platform of technology, tools, and teams that enables innovators to build and scale AI with confidence. Trusted by leading AI labs, startups, and global enterprises, CoreWeave combines superior infrastructure performance with deep technical expertise to accelerate breakthroughs and turn compute into capability. Founded in 2017, CoreWeave became a publicly traded company (Nasdaq: CRWV) in March 2025. Learn more at www.coreweave.com.What You'll Do: As a Senior Threat Intelligence Specialist I focused on protective security and geopolitical risks, you will support the collection, engineering, analysis, and dissemination of threat intelligence to corporate security, data center security, community engagement, and protective operations globally. You will bring familiarity of geopolitics, terrorism, instability, and transnational threat actors and deliver actionable intelligence to cross-functional stakeholders. About the role: • Support intelligence efforts for global operations, travel security, data center security, executive protection, and market expansion initiatives., • Monitor and assess global events including armed conflict, terrorism, political instability, sanctions, civil unrest, organized crime, regional escalation, and infrastructure disruption, translating developments into actionable business risk assessments., • Produce strategic, operational, and tactical intelligence products including forecasts, executive briefings, travel risk assessments, crisis updates, heat maps, geospatial overlays, dashboards, and early warning alerts., • Help build, integrate, and maintain intelligence collection pipelines using open-source intelligence, commercial intelligence feeds, geospatial data, proprietary sources, and third-party intelligence platforms., • Continually improve intelligence workflows, alerting mechanisms, and analytical tooling., • Partner cross-functionally with Global Security, Legal, Supply Chain, Strategy, Infrastructure, and business teams to operationalize intelligence and support risk-informed decision making., • Conduct post-incident analysis and lessons-learned reviews following geopolitical events, operational disruptions, or security incidents., • Contribute to best practices, technical standards, and scalable processes for geopolitical and operational threat intelligence., • Support relationships with external intelligence vendors, industry peers, academic institutions, and government or law enforcement partners, where appropriate., • Share domain knowledge, and contribute to continuous improvement of the team.Who You Are:, • Bachelor's degree in International Relations, Security Studies, Political Science, Computer Science, Engineering, or equivalent. Advanced degree preferred., • 5+ years of experience in threat intelligence, geopolitical risk analysis, physical security, or related domain., • Strong working knowledge of the threat intelligence lifecycle: requirements development, collection, processing, analysis, production, dissemination, feedback., • Good knowledge of geopolitical risk, state instability, terrorism, organized crime, and regional dynamics., • Experience operationalizing intelligence in support of security operations (travel, crisis, executive protection, facility security)., • Excellent communication skills: ability to brief, distill complex scenarios into actionable recommendations, write polished reports., • Demonstrated use of AI tools and large language models to accelerate research, analysis, drafting, and workflow automation., • Strong judgment, intellectual autonomy, and ability to manage ambiguous, fast-evolving environments., • Willingness to travel (regional or international) when required to support field operations or site assessments.Preferred:, • Experience supporting critical infrastructure, hyperscale environments, technology companies, or global corporate security programs., • Experience with intelligence automation, APIs, scripting, or data engineering using Python, SQL, or related technologies., • Experience supporting market entry assessments, protective intelligence, or global crisis management programs., • Certifications such as Certified Threat Intelligence Analyst (CTIA), GIAC (GISP, GCTI), or relevant government/intel community credentials., • Experience with vendor management and intelligence partnerships. Wondering if you're a good fit? We believe in investing in our people, and value candidates who can bring their own diversified experiences to our teams – even if you aren't a 100% skill or experience match. Why CoreWeave? At CoreWeave, we work hard, have fun, and move fast! We're in an exciting stage of hyper-growth that you will not want to miss out on. We're not afraid of a little chaos, and we're constantly learning. Our team cares deeply about how we build our product and how we work together, which is represented through our core values: • Be Curious at Your Core, • Act Like an Owner, • Empower Employees, • Deliver Best-in-Class Client Experiences, • Achieve More Together We support and encourage an entrepreneurial outlook and independent thinking. We foster an environment that encourages collaboration and enables the development of innovative solutions to complex problems. As we get set for takeoff, the organization's growth opportunities are constantly expanding. You will be surrounded by some of the best talent in the industry, who will want to learn from you, too. Come join us! The base salary range for this role is $134,000 to $179,000. The starting salary will be determined based on job-related knowledge, skills, experience, and market location. We strive for both market alignment and internal equity when determining compensation. In addition to base salary, our total rewards package includes a discretionary bonus, equity awards, and a comprehensive benefits program (all based on eligibility). What We Offer The range we've posted represents the typical compensation range for this role. To determine actual compensation, we review the market rate for each candidate which can include a variety of factors. These include qualifications, experience, interview performance, and location. In addition to a competitive salary, we offer a variety of benefits to support your needs. The benefits below reflect our US-based offerings; for roles in other locations, benefits vary and are shared during the hiring process. These include: • Medical, dental, and vision insurance - 100% paid for by CoreWeave, • Company-paid Life Insurance, • Voluntary supplemental life insurance, • Short and long-term disability insurance, • Flexible Spending Account, • Health Savings Account, • Tuition Reimbursement, • Ability to Participate in Employee Stock Purchase Program (ESPP), • Mental Wellness Benefits through Spring Health, • Family-Forming support provided by Carrot, • Paid Parental Leave, • Flexible, full-service childcare support with Kinside, • 401(k) with a generous employer match, • Flexible PTO, • Catered lunch each day in our office and data center locations, • A casual work environment, • A work culture focused on innovative disruption California Applicants California Consumer Privacy Act Equal Opportunity & Accommodations CoreWeave is an equal opportunity employer, committed to fostering an inclusive and supportive workplace. All qualified applicants and candidates will receive consideration for employment without regard to race, color, religion, sex, disability, age, sexual orientation, gender identity, national origin, veteran status, or genetic information. As part of this commitment and consistent with the Americans with Disabilities Act (ADA), CoreWeave will ensure that qualified applicants and candidates with disabilities are provided reasonable accommodations for the hiring process, unless such accommodation would cause an undue hardship. If reasonable accommodation is needed, please contact: careers@coreweave.com. Export Control Compliance This position requires access to export controlled information. To conform to U.S. Government export regulations applicable to that information, applicant must either be (A) a U.S. person, defined as a (i) U.S. citizen or national, (ii) U.S. lawful permanent resident (green card holder), (iii) refugee under 8 U.S.C. § 1157, or (iv) asylee under 8 U.S.C. § 1158, (B) eligible to access the export controlled information without a required export authorization, or (C) eligible and reasonably likely to obtain the required export authorization from the applicable U.S. government agency. CoreWeave may, for legitimate business reasons, decline to pursue any export licensing process.

Job DescriptionDescription: length of assignment: 6 months Work hours per day: 8 hours (Monday through Friday; 40 hours/week) Interview Process: Teams (other arrangements possible as needed) Job Responsibilities: • Perform analysis of samples and raw materials using chromatographic, spectroscopic, wet chemistry, physical testing and other analytical techniques. Techniques utilized include specific gravity, viscosity, potentiometric titrations, Karl Fisher, TLC, pH, liquid chromatography, gas chromatography, FTIR, others., • Apply existing test methods and procedures to complete the required analytical testing., • Collects, process and interpret accurately results, derive conclusions based on sound science, and prepare reports to effectively communicate results and findings to key stakeholders (audience with and without scientific backgrounds)., • Perform root cause analyses for non-conformance events related to laboratory testing., • Communicate effectively with management regarding testing statuses of projects., • Adhere to written procedures and practices to ensure good quality, compliance, and safety., • Ability to quickly adapt to changes, delays, or other unexpected events, and prioritize the work to ensure on time delivery of results and critical project milestones., • Communicate effectively with management regarding testing statuses of projects., • Adhere to written procedures and laboratory practices to ensure good quality and compliance., • Adhere to site and department’s health and safety guidelines and maintain personal and shared workspace., • Adapt to changes, delays, or other unexpected events, and prioritize the work to ensure on time delivery of results and critical project milestones. Qualifications: • Bachelor’s degree in Chemistry, or related field, with 1-3 years of professional experience, • Working knowledge of pH, TLC, Auto-titrators, FT-IR, Karl Fisher, Viscosity, and along with other wet chemistry analysis., • HPLC experience (preferred) and GC experience, • Strong written and verbal communication skills required., • Demonstrate ability to work in a diverse environment to manage multiple projects simultaneously and meet timelines., • Capability of working independently as well as working in a fast paced team driven environment, • Excellent bench skills and organization while maintaining a safe work environment., • Experience with Empower, ELN and LIMS software preferred, • Basic knowledge of the Microsoft Office Suite Requirements: length of assignment: 6 months Work hours per day: 8 hours (Monday through Friday; 40 hours/week) Interview Process: Teams (other arrangements possible as needed) Job Responsibilities: • Perform analysis of samples and raw materials using chromatographic, spectroscopic, wet chemistry, physical testing and other analytical techniques. Techniques utilized include specific gravity, viscosity, potentiometric titrations, Karl Fisher, TLC, pH, liquid chromatography, gas chromatography, FTIR, others., • Apply existing test methods and procedures to complete the required analytical testing., • Collects, process and interpret accurately results, derive conclusions based on sound science, and prepare reports to effectively communicate results and findings to key stakeholders (audience with and without scientific backgrounds)., • Perform root cause analyses for non-conformance events related to laboratory testing., • Communicate effectively with management regarding testing statuses of projects., • Adhere to written procedures and practices to ensure good quality, compliance, and safety., • Ability to quickly adapt to changes, delays, or other unexpected events, and prioritize the work to ensure on time delivery of results and critical project milestones., • Communicate effectively with management regarding testing statuses of projects., • Adhere to written procedures and laboratory practices to ensure good quality and compliance., • Adhere to site and department’s health and safety guidelines and maintain personal and shared workspace., • Adapt to changes, delays, or other unexpected events, and prioritize the work to ensure on time delivery of results and critical project milestones. Qualifications: • Bachelor’s degree in Chemistry, or related field, with 1-3 years of professional experience, • Working knowledge of pH, TLC, Auto-titrators, FT-IR, Karl Fisher, Viscosity, and along with other wet chemistry analysis., • HPLC experience (preferred) and GC experience, • Strong written and verbal communication skills required., • Demonstrate ability to work in a diverse environment to manage multiple projects simultaneously and meet timelines., • Capability of working independently as well as working in a fast paced team driven environment, • Excellent bench skills and organization while maintaining a safe work environment., • Experience with Empower, ELN and LIMS software preferred, • Basic knowledge of the Microsoft Office Suite

Job Description About the Role Innovation Labs is seeking a motivated and detail-oriented Associate Chemist to join our Quality Control team. This is an excellent opportunity for a recent graduate or early-career scientist looking to gain hands-on experience in a fast-paced contract manufacturing environment. In this role, you will perform analytical testing on a wide range of products, including cosmetics, skincare, OTC drug products, and dietary supplements. You will work closely with experienced chemists and cross-functional teams while developing your technical expertise in laboratory operations, quality systems, and regulatory compliance. Hourly Wage: $22-$25 Key Responsibilities • Analytical Testing – Perform routine testing of raw materials, in-process samples, and finished products using techniques such as HPLC, UV-Vis spectroscopy, FTIR, titrations, and other laboratory methods., • Sample Preparation & Analysis – Prepare samples, standards, and reagents according to approved procedures and specifications., • Data Review & Documentation – Accurately document test results, maintain laboratory notebooks, and complete records in compliance with cGMP requirements., • Instrument Operation & Maintenance – Operate, calibrate, and perform routine maintenance of laboratory instrumentation., • Quality & Compliance – Follow SOPs, safety procedures, and quality standards in accordance with cGMP, FDA, and company requirements., • Stability Testing Support – Assist with stability studies and sample management programs., • Investigation Support – Participate in laboratory investigations, troubleshooting activities, and corrective action initiatives under the guidance of senior staff., • Cross-Functional Collaboration – Work with Quality Assurance, R&D, Production, and Regulatory teams to support product quality and manufacturing operations., • Continuous Improvement – Contribute to laboratory efficiency, organization, and process improvement initiatives. Requirements Qualifications • Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline., • 0–2 years of laboratory experience (internships, co-ops, academic research, or industry experience welcomed)., • Basic understanding of analytical chemistry principles and laboratory techniques., • Familiarity with laboratory instrumentation such as HPLC, UV-Vis, FTIR, or related analytical equipment., • Strong attention to detail and organizational skills., • Ability to accurately record, review, and interpret analytical data., • Excellent written and verbal communication skills., • Ability to work independently and collaboratively in a team environment. Preferred Qualifications • Internship, co-op, or laboratory experience in pharmaceuticals, cosmetics, personal care, food, or dietary supplement industries., • Exposure to cGMP, GLP, or regulated laboratory environments., • Familiarity with chromatographic techniques, including HPLC., • Experience using Microsoft Excel and laboratory data management systems., • Strong problem-solving skills and a willingness to learn new analytical techniques. What You'll Gain • Hands-on experience with industry-standard analytical instrumentation., • Exposure to a diverse portfolio of cosmetic, skincare, OTC, and dietary supplement products., • Mentorship from experienced scientists and quality professionals., • Opportunities for career growth and advancement within a rapidly expanding organization., • Experience working in a regulated manufacturing environment with direct impact on product quality and consumer safety. Benefits • Comprehensive Health Benefits package (Medical, Dental, Vision, Life, AD&D), • Competitive 401(k) match, • Paid time off (Vacation, Sick, Holiday, Summer Fridays), • Monthly birthday celebrations + other fun activities!, • Daily subsidized meals iLABS (Innovation Labs) Inc. is an equal opportunity employer. We do not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other characteristic protected by federal, state or local laws. All employment is decided on the basis of qualifications, merit, and business need.

Job DescriptionAt Weston Solutions, Inc. you will do meaningful work and make valuable contributions. Employee ownership at Weston is a path to professional growth and access to diverse opportunities in a highly connected community that works together across key service areas to make a difference in the environment. Weston has continued to evolve and adapt to our changing world as a premier provider of environmental and infrastructure services for over sixty years. In both the public and private sectors our teams help identify, solve, mitigate, and manage critical environmental issues to help clients achieve a more sustainable future.Weston is seeking an experienced Senior Laboratory Chemist to support the EPA Response Engineering Analytical Contract (REAC), providing critical analytical support during environmental emergencies and Superfund projects. This role supports time-sensitive investigations across diverse sample matrices including air, soil, water, and oil, in both fixed and mobile laboratory environments.The Senior Laboratory Chemist serves as a technical expert, partnering with project teams and clients to deliver high-quality analytical data in support of environmental response and remediation efforts.Location: Edison, New JerseyExpected Outcomes • Execute GC/MS analyses of organic compounds across multiple environmental matrices in both fixed and mobile laboratory settings, • Deliver accurate, defensible analytical data using EPA methods (e.g., 8260, 8270, TO-15, 8082A) within required turnaround times, • Prepare and process samples, standards, and reagents using appropriate extraction and preparation techniques (e.g., liquid-liquid extraction, Soxhlet/Soxtherm, solid-phase extraction), • Interpret and evaluate mass spectral data to identify compounds using spectral libraries and sound analytical judgment, • Produce clear, concise, and technically accurate analytical reports for clients and project teams, • Maintain and troubleshoot analytical instrumentation to ensure performance, reliability, and data integrity, • Develop, optimize, and validate analytical methods using GC systems equipped with detectors such as FID, PID, and MS, • Ensure safe handling, storage, and management of hazardous materials in compliance with laboratory and regulatory requirementsKnowledge, Skills & Abilities, • Bachelor of Science (BS) degree in Chemistry or a closely related discipline, including at least 30 credit hours in chemistry, • Minimum of 10 years of analytical chemistry experience, including at least 5 years of hands-on instrumentation experience, • Strong knowledge of organic chemistry, chromatography, and mass spectrometry principles, • Experience with SW-846 methods for organic analysis in soil, water, and oil, • Experience working with Laboratory Information Management Systems (LIMS), • Understanding of hazardous waste characterization, storage, and labeling requirementsPreferred Qualifications, • Experience with Toxic Organic (TO) air methods, • Knowledge of vapor intrusion sampling techniques, including passivated (Summa) canisters and Tedlar bags, • Familiarity with the Incident Command System (ICS) framework (ICS 100, 200, 700, 800); certification preferred, • 40-hour HAZWOPER certification, • Strong knowledge of EPA analytical methods and environmental regulations, • Strong organizational, communication, and problem-solving skills, • Proficiency in Microsoft Office (Outlook, Word, Excel), • Ability to work independently and manage multiple priorities in a fast-paced environment, • Willingness to travel for field assignments, including mobile laboratory deploymentsWe fully invest in our people: Weston provides a generous, comprehensive benefits package program that offers employees high value options with solid financial protection, meeting the personal needs of its people and their families., • Medical, Dental, Vision, 401K with base and matching employer stock contributions., • Paid time off includes personal, holiday and parental., • Life and disability plans., • Critical illness and accident plans., • Work/Life flexibility., • Professional development opportunities.Compensation will vary based upon experience, education, skill level, and other compensable factors. d other compensable factors.

Job DescriptionJob Title: NMR ChemistJob Description The NMR Chemist supports synthetic polymer characterization using NMR spectroscopy to enable new product research, product development, product registrations, manufacturing investigations, field issue resolution, and lifecycle management. This role focuses on daily sample preparation, NMR data acquisition, data interpretation, and accurate documentation of results, while contributing to a well-organized and safe laboratory environment. Responsibilities • Prepare test articles and samples for NMR analysis, including more complex preparations beyond simple small-molecule mixtures when required., • Conduct NMR testing in accordance with validated test methods and experimental designs., • Document all testing activities in a laboratory notebook, ensuring clear, complete, and traceable records of methods, observations, and results., • File all documentation in alignment with standard operating procedures and enter test results into the laboratory information management system (LIMS)., • Perform NMR analyses to evaluate polymer composition, impurity profiles, and to identify and quantify degradation products., • Support NMR characterizations related to extractables and leachables, manufacturing issues, field issues, and other chemical composition questions across the product lifecycle., • Analyze NMR data, interpret spectra, and summarize findings in a clear and concise manner., • Report results by compiling data, typically in spreadsheets, and ensure raw data are properly stored and filed., • Routinely monitor laboratory supply inventory and place orders through approved vendors to prevent shortages that could delay studies., • Perform monthly laboratory safety inspections and document findings in accordance with established instructions., • Maintain good laboratory housekeeping by regularly organizing workspaces, equipment, and materials., • Contribute to general lab duties, including organizing inventory and verifying adequate supplies to support daily operations.Essential Skills, • Hands-on experience with NMR spectroscopy, including at least three months of independently running and interpreting NMR spectra., • Demonstrated experience in sample preparation for NMR or related analytical techniques., • Proficiency in documenting experimental work and results in a laboratory notebook on a regular basis, in either academic or industrial settings., • Experience using TopSpin software for NMR data acquisition and processing., • Proficiency with Excel for organizing, analyzing, and reporting data., • Bachelor’s degree (BS) in chemistry or a related field., • Foundational knowledge in chemistry, with a preference for chemical or organic chemistry background., • Ability to collect and interpret a substantial number of NMR spectra, demonstrating familiarity with routine data acquisition workflows., • Strong attention to detail and commitment to following validated test methods and standard operating procedures., • Ability to manage multiple tasks in a laboratory setting, including testing, documentation, and inventory-related activities.Additional Skills & Qualifications, • Exposure to synthetic polymer NMR characterization or a strong interest in developing expertise in this area; on-the-job training will be provided for polymer NMR spectra and characterization., • Experience supporting technical report writing or authoring sections of technical reports, particularly related to analytical findings., • Experience with more complex sample preparation beyond small-molecule mixtures., • Familiarity with laboratory safety practices, including participation in safety inspections., • Interest in working across the full product lifecycle, from early research through field support., • Willingness to learn and adapt to new analytical methods, software tools, and laboratory processes.Work Environment This is an onsite laboratory-based role, working Monday through Friday. The position is considered essential, so the NMR Chemist will be present on-site regardless of broader site status. The NMR laboratory focuses on synthetic polymer NMR characterizations and supports a wide range of activities, including new product research, product development, product registrations, manufacturing troubleshooting, field issue investigations, and lifecycle management. The typical workweek involves daily sample preparation, NMR data collection using TopSpin, data analysis, data reporting primarily via spreadsheets, and thorough documentation of findings in a lab notebook. The environment emphasizes strong safety practices, including monthly safety inspections, and requires regular housekeeping and organization of inventory to ensure adequate supplies. The role provides exposure to all phases of the product lifecycle and offers training in synthetic polymer NMR spectrometry within a structured, process-driven laboratory setting. Job Type & Location This is a Contract position based out of Raritan, NJ. Pay and Benefits The pay range for this position is $33.00 - $39.50/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Raritan,NJ. Application Deadline This position is anticipated to close on Jul 31, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Role Purpose: Works in the Innovation R&D Lab developing new formulations to support the Innovation Pipeline, concept formulas for TRIssential Kits and optimizing existing TRIssential Kits based on the guidance from the Technical Marketing, and Business Development. This role also provides technical support to customer inquiries, with emphasis on how to use Tri-K ingredients and how to troubleshoot formulas containing Tri-K ingredients. Position Reports to: Innovation R&D Manager Positions Reporting to this Position: none Role Objectives: Essential Duties and Responsibilities include the following. Other duties may be assigned. • Design, develop, and test new skin care (and possibly hair care), and personal care formulas for the Innovation Pipeline, and TRIssential Library, supporting the business needs., • Improve and update existing TRIssential library formulas based on the market trend, customer needs, and the guidance from sales, marketing and business management teams., • Conduct stability tests on new formulas and re-run stability on existing formulas as necessary., • Generate formula sheets for new formula developments and update existing formula sheets as necessary., • Manage formula safety studies – RIPT, Micro PET, etc., • Collaborate with Regulatory team to ensure global compliance of the formulas., • Conduct stability tests on Tri-K ingredients and vendor supplied material for shelf-life verification and recertification., • Conduct formula application tests – in vitro SPF, texture evaluation, foam test, spray pattern evaluation, packaging compatibility test, etc., • Generate technical data sheets from the application aspect of Tri-K ingredients., • Generate formulas for Tri-K ingredient testing and competitive analysis., • Work closely with various departments within the organization, becoming an integral partner in the Sales-Marketing-Technical Triangle., • Provide technical/laboratory support to Technical Support, Sales, Marketing, Business Development, and other departments., • Work closely with the Protein Division to optimize the formulation compatibility of the Tri-K Protein products., • Prepare samples for samples inventory, • Analyze and evaluate competitive products, • Provide formula application technical support to customers, • Run existing product revamp projects., • Develop prototype formulas for formulary, • Prepare finished formulations for demonstration and testing purposes, • Participate in designing and conducting experiments to generate basic information about new and existing raw materials, • Develop new applications for existing materials and technologies, • Evaluate new raw materials and technologies in multiple applications, • Evaluate new / alternate vendors of existing TRI-K products, • Design and conduct experiments to resolve quality complaints, • Design, coordinate, and execute efficacy studies for TRI-K products Competencies: To perform the job successfully, an individual should demonstrate the following competencies: • Formulation, • Expertise in generating skin care formula forms such as w/o emulsions, o/w emulsions, w/s emulsions, gels, oils, anhydrous formulas, surfactant cleansers, oil cleansers, emulsion cleansers, waxes, balms, hot pour formulas, cold process formulas, clean & green formulas, vegan formulas, OTC formulas, etc., • Expertise in FDA OTC monographed cosmetic formulas., • Expertise in formulation technical knowledge – HLB, pKa, isoelectric point, lamellar structure, pH effect, ion effect, metal chelation, ionic vs non-ionic emulsifiers, thixotropy, polymer actives, polymer non-actives, preservatives, solubility vs melting behaviour in cosmetic formulations, solubilizers, effect of refractive of index on emulsions, etc., • Formula Evaluation Method Knowledge, • in vivo SPF, critical wavelength, water resistance, • Micro content, micro PET, RIPT, • Analytical - Synthesizes complex or diverse information., • Problem Solving - Gathers and analyses information skilfully., • Oral Communication - Listens and gets clarification; Demonstrates group presentation skills., • Written Communication - Writes clearly and informatively., • Quality Management - Demonstrates accuracy and thoroughness., • Adaptability - Manages competing demands., • Dependability - Completes tasks on time or notifies appropriate person with an alternate plan., • Initiative - Undertakes self-development activities., • Planning/Organizing - Prioritizes and plans work activities; Uses time efficiently., • Safety and Security - Uses equipment and materials properly., • Demonstrates ownership and accountability Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education/Experience: A Bachelor’s degree in Chemistry or a related technical discipline; minimum of 3 years of experience and/or training in related/relevant field. We offer a competitive compensation package including: • Medical, • Dental, • 401 (K), • Vision, • Paid Time Off, • Life Insurance, • In addition to other programs and plans

Job DescriptionPosition Description: Position Summary:The Quality Control Chemist-I is responsible for conducting routine testing and analysis of raw materials, in-process materials, and finished product samples using various analytical methodologies to ensure the quality of dietary supplements and OTC products. This role includes reviewing and maintaining Standard Operating Procedures (SOPs), Testing Procedures, calibrations, and other controlled documents to ensure compliance with regulatory standards and internal procedures. Additionally, the Chemist-I will assist in quality control stability testing and contribute to maintaining accurate records and documentation.DUTIES AND RESPONSIBILITIES:Ensure all work is performed in compliance with cGMP, GLP, compendia standards, and internal procedures. Conduct wet chemistry and analytical testing on raw materials, finished products, in-process samples, stability, and packaged products according to Testing Procedures.Assist in quality control stability testing, prepare, and maintain stability records and summaries.Operate, maintain, and troubleshoot analytical instruments, including pH meter, FTIR, TOC, UV, and others as necessary.Maintain accurate records of all analyses, ensuring contemporaneous documentation and adherence to company standards.Perform laboratory analysis right the first time and ensure all results are properly documented.Conduct laboratory investigations under the guidance of laboratory management.Work effectively under the direction of supervisors and/or manager, and perform additional duties as required.QUALIFICATION AND EXPERIENCE:Bachelor’s degree in chemistry, Biochemistry, Pharmaceutical Sciences, or related field with 0 - 3 years of relevant experience in a quality control setting; or an equivalent combination of education and experience.Basic understanding of Current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), and quality control principles in the pharmaceutical industry.Math skills commensurate with a scientific background are required.Ability to communicate test results and observations clearly, both verbally and in writing. Ability to follow written instructions and solve basic analytical problems using standard procedures.

Job Description SUMMARY: Plans and conducts activities for new product development and for maintaining and improving existing technology. RESPONSIBILITIES: Main Strategic Responsibilities • Responsible for the planning and execution of work on multiple testing, maintaining and improving projects including supporting new product development at the direction of the VP Technology or Senior Research Scientist. Specific Day to Day Responsibilities • Plans and carries out technical work to support new technology and to improve existing technology, • Uses appropriate techniques, apparatuses, and procedures to achieve objectives, • Achieves a thorough understanding of products, testing methods, and raw materials, • Responsible for managing all Technical Service Requests for testing, maintaining, and improving existing products, • Troubleshoots existing products, including modifying current prototypes as needed, • Carries out work to qualify new raw materials and new sources of raw materials, • Assures product performance during installation and in end-use conditions, • Maintains organized, accurate and retrievable records of all work, • Composes written reports in a timely manner to communicate and document the work done, • Reports and communicates the results of work to Senior Research Scientist and/or department head as often as necessary, • Designs and carries out experiments in the laboratory, fire-test-furnaces, manufacturing facility, and application equipment (such as paint sprayers), etc., • Maintains compliance with ISO 9001 / 2008 requirements for “Design and Development”, • Maintains a suitable laboratory and the accuracy of equipment, • Maintains a clean and organized work environment, • Complies with corporate health and safety practices, • Directly supervise and mentor technicians. Indirectly manage other Technology personnel, as necessary to accomplish project goals. JOB TITLES DIRECTLY SUPERVISED: Technician, Sr. Technician, Technical Specialist SCOPE OF POSITION: Is accountable for contributing to the assessment, development, reformulation, maintenance, and enhancement of existing products through planning, executing, and analysis of experiments with clear and accurate results. Responsibilities typically occur in the Company’s R&D facility in Stanhope, NJ, but may occur anywhere in the world. Some travel is required to manufacturing facilities, courses, and testing labs EXPERIENCE: Bachelor’s degree in Chemistry or Polymer Science (preferred) or Material Science KNOWLEDGE: College-level Organic, Inorganic, Analytical and Physical Chemistry, and ideally, Material/Polymer Science desired SKILLS: • Ability to work within a team environment, • Establish questions and generates recommendations, • Inventiveness and problem-solving abilities, • Ability to quickly react to negative or positive research results, • Aptitude with equipment and machines, • Be organized and be able to carry out multiple projects simultaneously from start to finish, • Be able to understand technical issues and evaluate alternate solutions, • Development and refinement of new test methods and characterization techniques, • Proficient with Microsoft Office and be able to apply mathematical concepts, • Strong communication skills in verbal, written and presentation form, • Self-motivated and willing to work “hands-on” in laboratory, • Strong ownership with the ability to work under pressure, • Ability to supervise and mentor direct reports, • Be able to work atypical hours and travel, sometimes internationally The base salary anticipated is $130,000 - $150,000 per year for this position at the time of this posting. Consistent with applicable law, actual compensation may vary and will be determined by several factors, including but not limited to, the applicant’s skills, qualifications, experience, and other job-related factors. Isolatek International reserves the right to modify this pay range at any time. An employee may also be eligible for annual discretionary incentive compensation based on company and personal performance. Isolatek offers a wide range of employee benefits, including health insurance, life insurance, disability insurance, paid time off, sick leave, vacation, and 401(k), in addition to other benefits. This job description is not intended to contain a comprehensive listing of activities, duties, or responsibilities that are required for this position. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice. Isolatek is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, creed, religion, national origin, sex, sexual orientation, gender identity and expression, age, disability, veteran status, or any other protected factor. No phone calls, please.

Job Description Geo-Technology Associates, Inc. (GTA) is seeking a full-time Field Geologist for tour Somerset, New Jersey office. Responsibilities will include construction observation and testing of soil, concrete, and other materials. GTA will provide you with Personal Protective Equipment, which includes a High Visibility Vest, Hard Hat, Gloves, and Safety Glasses. Hours of work are Monday through Friday, 7 AM to 4 PM. Overtime should be expected and is paid at time and a half. Occasional weekend work may be required. This is an excellent opportunity for training, certifications, and career growth! Requirements • High School Diploma or College Degree, • Ability to lift 60 pounds or more on a regular basis, • Previous Soils Testing experience desired, • Own Reliable Transportation, • Good Driving Record NOTE: This position may require standing for extended periods as well as repetitive motions such as lifting or hammering. The employee must have the ability to use their hands to handle, finger or feel; reach, climb or balance; crouch, stoop, crawl, kneel and sit, see and smell; including close, distance and peripheral vision, depth vision and ability to focus. Benefits • Competitive Salary, Paid Time Off, Paid Holidays, • Yearly bonus potential, • Medical, Dental, Vision, Health Savings Account, Flexible Spending, • Life Insurance, Short- and Long-Term Disability Insurance, • 401(k) with Company Match, • Educational Assistance Program, • Free membership to professional societies, • Professional Growth & Advancement – we’ll help you get there! - Seminars, Conventions, Lunch & Learns, Mentoring, Software Training, • Employee Referral Bonuses, • Employee Recognition Program, • Company picnics and events and a great working environment! We ensure nondiscrimination and equal employment opportunity in all programs and activities in accordance with Title VI of the Civil Rights Act of 1964, and all revisions and addendums thereof. #LI-Onsite #GTAworkable

Client Overview Our client, a leading consumer products organization focused on developing innovative, science-driven personal care solutions, is seeking a Hair Care Formulation Chemist to drive the creation and optimization of high-performance hair care products. The company combines advanced research, consumer insights, and cutting-edge ingredient technologies to deliver products that meet evolving market needs and consumer expectations.\n \n Salary/Hourly Rate $70k - $80k\n \n Position Overview The Hair Care Formulation Chemist is responsible for developing, optimizing, and commercializing innovative hair care products, with a focus on treatments, styling products, fixatives, shampoos, and conditioners. The Hair Care Formulation Chemist leverages deep expertise in formulation science, hair biology, and ingredient technologies to create high-performing products while collaborating cross-functionally to ensure successful scale-up, regulatory compliance, and continuous innovation. The Hair Care Formulation Chemist is fully on-site 5 days a week. Occasional domestic travel is required for the Hair Care Formulation Chemist.\n \n Responsibilities Of The Hair Care Formulation Chemist \n\n • Formulate, improve, and evaluate innovative hair care products, including treatments, styling aids, and fixative systems.\n, • Design and create new formulation platforms (chassis) to support product innovation and pipeline development.\n, • Lead product development across a variety of packaging formats and delivery systems.\n, • Conduct in-depth research on ingredient functionality, hair fiber science, and emerging technologies to improve product performance, consumer benefits, and sensory attributes.\n, • Design, execute, and analyze experiments to assess product stability, compatibility, and overall performance.\n, • Collaborate closely with cross-functional teams, including Product Development, Regulatory, Quality, and Manufacturing, to translate consumer insights into effective, science-based product solutions.\n, • Prepare and maintain technical documentation, including formulation procedures, raw material specifications, stability protocols, and manufacturing batch records.\n, • Ensure all formulations comply with applicable regulatory, safety, and quality standards.\n, • Provide technical expertise in resolving formulation challenges and support the scale-up of products from laboratory development through pilot and commercial production.\n, • Contribute to the advancement of organizational expertise in hair science, formulation technologies, and best practices.\n, • Stay informed of industry trends, emerging technologies, competitive products, and new raw materials to identify opportunities for continuous innovation. \nRequired Experience/Skills For The Hair Care Formulation Chemist \n\n • Minimum of 4 years of hands-on formulation experience within hair care research and development.\n, • Working knowledge of shampoo and conditioner formulations.\n, • Strong understanding of colloid and surface chemistry, emulsion technology, rheology, polymer science, and their applications in hair care formulations.\n, • Demonstrated success in developing, commercializing, and launching hair care products in the marketplace.\n, • Experience conducting stability, compatibility, and performance testing, with knowledge of claims substantiation and consumer evaluation methodologies.\n, • Familiarity with formulation scale-up processes and collaboration with contract manufacturing partners.\n, • Working knowledge of cosmetic regulations, raw material compliance requirements, and global industry standards. \nPreferred Experience/Skills For The Hair Care Formulation Chemist \n\n • Strong analytical, problem-solving, project management, and communication skills.\n, • Ability to thrive in a fast-paced, collaborative, and innovation-driven environment. \nEducation Requirements \n\n • Bachelor’s or Master’s degree in Cosmetic Science, Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related scientific discipline is required. \nBenefits \n\n • Medical, dental, and vision insurance, including an HSA medical plan with an employer contribution.\n, • Pretax flexible spending for medical, dependent care, transit, and parking.\n, • 401(K) with match.\n, • PTO. \n

Description The Defense Sector at Leidos currently has an opening for a Synthetic Chemist to work at our Picatinny Arsenal, NJ site Conduct synthesis, scaleup, and characterization of novel materials. Primary Responsibilities. Conduct ongoing literature searches to develop and maintain awareness of latest ingredients, processes, and techniques. Design and execute novel approaches to the synthesis of new materials. Develop alternate more efficient methods for the synthesis of existing materials. Conduct process optimization and scale up studies for large scale preparation of these materials Characterize all materials utilizing state-of-the-art analytic techniques. Prepare technical report and presentations. Develop novel ideas and contribute to proposals. Basic Qualifications. BS/MS in organic chemistry with 2-6 years relevant experience. Demonstrated experience developing and executing synthesis of new materials. Knowledge and hands-on experience with analytical methods for the separation and characterization of materials to include chromatographic and spectroscopic techniques. Ability to work in a team-based environment. US Citizenship required. Preferred Qualifications. Higher degree preferred. Knowledge of energetic materials a plus. If you're looking for comfort, keep scrolling. At Leidos, we outthink, outbuild, and outpace the status quo — because the mission demands it. We're not hiring followers. We're recruiting the ones who disrupt, provoke, and refuse to fail. Step 10 is ancient history. We're already at step 30 — and moving faster than anyone else dares. May 13, 2026 For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above. Pay Range $59,150.00 - $106,925.00 The Leidos pay range for this job level is a general guideline only and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law. About Leidos Leidos is an industry and technology leader serving government and commercial customers with smarter, more efficient digital and mission innovations. Headquartered in Reston, Virginia, with 47,000 global employees, Leidos reported annual revenues of approximately $16.7 billion for the fiscal year ended January 3, 2025. For more information, visit _. Pay and Benefits Pay and benefits are fundamental to any career decision. That's why we craft compensation packages that reflect the importance of the work we do for our customers. Employment benefits include competitive compensation, Health and Wellness programs, Income Protection, Paid Leave and Retirement. More details are available at _. Securing Your Data Beware of fake employment opportunities using Leidos’ name. Leidos will never ask you to provide payment-related information during any part of the employment application process (i.e., ask you for money), nor will Leidos ever advance money as part of the hiring process (i.e., send you a check or money order before doing any work). Further, Leidos will only communicate with you through emails that are generated by the Leidos.com automated system – never from free commercial services (e.g., Gmail, Yahoo, Hotmail) or via WhatsApp, Telegram, etc. If you received an email purporting to be from Leidos that asks for payment-related information or any other personal information (e.g., about you or your previous employer), and you are concerned about its legitimacy, please make us aware immediately by emailing us at _. If you believe you are the victim of a scam, contact your local law enforcement and report the incident to the _. Commitment to Non-Discrimination All qualified applicants will receive consideration for employment without regard to sex, race, ethnicity, age, national origin, citizenship, religion, physical or mental disability, medical condition, genetic information, pregnancy, family structure, marital status, ancestry, domestic partner status, sexual orientation, gender identity or expression, veteran or military status, or any other basis prohibited by law. Leidos will also consider for employment qualified applicants with criminal histories consistent with relevant laws.

About Mercor’s talent network Join our Chemist Expert Network to connect with leading AI labs and companies seeking your expertise. About Mercor projects Experts in our network contribute to: - Training and evaluating AI models in Chemistry - Creating tasks and deliverables based on real-world

QA-ready reporting Maintain detailed, compliant documentation in accordance with FDA cGMP requirements Support method development, verification, validation, and transfer activities Participate in investigations including deviations, OOS/OOT, and CAPA Maintain laboratory equipment including calibrati

Clean Harbors in Linden is seeking an Environmental Field Chemist (CleanPack Chemist) to handle, segregate, pack, and inspect chemical waste in accordance with Federal/State/Local regulations and our company policies and procedures. The Environmental Field Chemist are (NOT) laboratory-based Chemist.

Function: Supply Chain Location: Morris Plains, New Jersey, US About The Wella Company: We enable individuals to look, feel, and be their true selves. Wella Company is one of the world's leading beauty companies, comprised of a family of iconic brands such as Wella Professionals, Clairol, OPI, Nioxin and ghd. With 6,000 employees globally, presence in over 100 countries, Wella Company and its brands enable consumers to look, feel, and be their true selves. As innovators in the hair and nail industry, Wella Company empowers its people to delight consumers, inspire beauty professionals, engage communities, and deliver sustainable growth to its stakeholders. Position Summary: The EXO NA Industrial Chemist is the Wella expert and SPOC for TPMs for any topic related to raw materials, formulations, and bulk manufacturing processes. The EXO NA Industrial Chemist owns and maintains all documentation, standards, and technical requirements that support the qualification and validation of suppliers and manufacturing sites producing our raw materials, intermediates, and finished products. This role enables the organizations, both internal and external, to drive business outstanding results through breakthrough solutions on raw materials and making processes. The Industrial Chemist supports cross-functional EXO teams in the qualification of new products and the maintenance of existing qualified processes, ensuring the delivery of cost- and cash-efficient products while maintaining sustainable results and the highest quality standards. Technologies to be managed are shampoos, conditioners, hair treatments (oils, sprays, aerosols, among others), hair color products and nail products across North America External Operations manufacturing partners, TPMs. Key Responsibilities: • Partner with R&D and Global/Local Initiative Teams to develop the Technical Learning Plan (Commissioning, Qualification, and Verification) for innovation and technical projects at North America TPMs., • Lead and execute the Technical Readiness Plan for all projects managed across North America TPMs., • Document and maintain records of Technical Learning Plan trials, validations, and qualifications., • Support Supply Chain, Quality Assurance, and Procurement teams in achieving service targets through the identification of alternative materials and process improvements., • Collaborate with Global R&D to design, implement, and sustain standard processes, systems, and technical requirements for manufacturing sites and the EXO organization., • Identify efficiency opportunities within incumbent manufacturing sites to drive cost savings, cash optimization, and sustainability improvements., • Influence and partner with manufacturing sites to identify, prioritize, and implement efficiency Qualifications: • Essential Bachelor's degree in Engineering (e.g., Chemical, Biotechnology, Industrial, Mechanical, or Product Development Engineering)., • 2 years of experience in the Professional Beauty, Personal Care, Consumer Goods, or Pharmaceutical industries, with exposure to bulk manufacturing processes, filling operations, formulation research and development, and/or laboratory analysis., • 2 years of project or program management experience, with a demonstrated track record of successful project delivery., • Strong teamwork, collaboration, and communication skills, with the ability to work effectively in remote, cross-functional, and multicultural environments., • Strong relationship-building and stakeholder management skills, with the ability to collaborate effectively with external partners and organizations., • Problem Solving Tools basic knowledge (e.g., 6W-2H, Ishikawa, RCA), • Capacity to handle frequent business travels (25% of time)., • Language: English Professional Working Proficiency., • Software: Microsoft Office Excel advanced skills., • Software: MS Word and MS PowerPoint basic skills., • Preferred Project Management certification (e.g., PMP, CAPM, PMI-ACP)., • Continuous Improvement basic knowledge (e.g., PDCA, 5S)., • Software: SAP associate (basic) level., • Continuous Improvement certification (e.g., Lean Manufacturing, 6 ?)., • Software: Microsoft Project intermediate skills., • Software: Microsoft Power BI beginner skills. Notices: All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status. If you need assistance and/or a reasonable accommodation due to a disability during the application process, please email NA.Recruiting@wella.com. This email account will not respond to inquiries regarding the status of a candidate's application. Wella participates in the E-Verify Program to confirm eligibility to work in the United States. Information regarding your rights: Know your rights and Pay Transparency Nondiscrimination Provision. We disclose the compensation range for positions in compliance with local law. Actual salaries will vary and may be above or below the range based on various factors including but not limited to location, experience, skills and in comparison to internal incumbents currently in similar roles. Pay Range: $91,500 - $122,000 salary per year. The range listed is just one component of Wella Company's total rewards package for employees. Other rewards may include annual bonus plan or variable pay, depending on the role. In addition, Wella Company provides a rich variety of benefits to employees, including health insurance, life and disability insurance, 401(k) retirement plan, paid holidays and paid time off (PTO).

This position is responsible for ensuring the quality and compliance of chemical products through rigorous testing and analysis. The role involves working closely with cross-functional teams to develop and implement quality control procedures, maintaining detailed records of testing results, and ensuring all products meet specified standards before release.

As a QC Chemist, you will be responsible for performing day-to-day laboratory activities under prescribed procedures, including qualitative and quantitative analysis, solution preparation, calibration, qualification, and maintenance of laboratory instrumentation. You will also conduct environmental monitoring, assist with technical writing, and perform administrative tasks. Additionally, you will contribute to solving problems, reviewing experimental data, writing protocols/SOPs/validation reports, and training support staff as necessary. You will monitor study procedures to ensure data accuracy and report quality while maintaining a GMP/GLP laboratory. • Conduct analysis in compliance with cGMP requirements, compendia standards, and internal procedures., • Maintain accurate records of analysis and perform documentation to company standards., • Prepare test solutions, volumetric solutions, and samples used in analysis., • Perform assigned sampling, physical, chemical tests and assays on raw materials, active pharmaceutical ingredients, in-process, finished bulk, finished product, and stability products analysis in an FDA regulated lab environment., • Use a variety of analytical instruments such as HPLC, GC, Dissolution, Malvern particle size analyzer, IR, Auto Titrator, UV Spectrophotometer, KF, Potentiometer, etc., • Perform analysis with a practical understanding of the test procedure and instrument operation., • Conduct laboratory investigations under the supervision of the laboratory manager., • Perform maintenance and calibrations of laboratory instruments/equipment., • Comply with all regulatory and in-house requirements including safety, housekeeping, laboratory chemical waste, cGMP, cGLP, and documentation., • Maintain the required level of training needed to perform GMP tasks., • Prepare and/or review test procedures, SOPs, and protocols as assigned., • Proficiency in current Good Manufacturing Practices (cGMP), FDA, and other regulatory requirements., • Experience with analytical techniques such as Dissolution, FT-IR, GC, UV-VIS, KF, TLC., • Knowledge of computer applications and programs related to laboratory applications such as HPLC, FTIR, TOC., • Familiarity with sampling methods and quality control systems., • Understanding of mathematics including statistics., • Proficiency in sample preparation techniques, spectroscopic techniques, and chromatographic systems., • Basic computer knowledge including MS Word, Excel, and Outlook., • 3-5 years of routine testing using HPLC and Dissolution., • Experience with solid oral dosage and focus on raw material, finished product., • Pharma GMP experience, laboratory, wet chemistry, titration, chromatography., • Bachelor's or master's degree in Pharmaceutical, Biological, Chemical science or related field., • 5-6 years of related laboratory work experience; minimum of 5 years as a QC Chemist in a GMP environment., • Ability to work successfully in both a team/matrix environment and independently., • Ability to work in a fast-paced environment, manage priorities and maintain timelines for multiple projects., • Ability to work safely in a chemical laboratory., • Ability to perform basic calculations, read, write, communicate, and handle stress produced by time pressure, customer demands, etc., • Must be able to access all laboratory, manufacturing, and office areas., • Must be able to wear the required PPE for entering laboratory and processing areas., • Specific vision requirements include reading written documents and using a computer., • Ability to sit or stand for prolonged periods and occasionally lift up to 25 lbs. with or without assistance. You will be working in a laboratory setting with approximately 10 people. The laboratory is equipped with modern instrumentation and follows strict safety and regulatory protocols. The work environment requires wearing personal protective equipment (PPE) and involves standing or sitting for prolonged periods. The laboratory operates under a fast-paced and dynamic atmosphere, providing an excellent opportunity for growth and development. The pay range for this position is $30.00 - $40.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) This is a fully onsite position in Cranbury, NJ. This position is anticipated to close on Apr 30, 2025. Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes, • Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

College of Liberal Arts, Department of Political, Social and Cultural Sciences Adjunct Faculty Kean University in Union, New Jersey has grown into a comprehensive, global institution of higher education serving a diverse enrollment of nearly 19,0000 students worldwide.

Develop a working understanding of H&A's other consulting practice areas and actively support marketing other additional services to existing clients.

Managing Consultant, Engineer/Geologist/Scientist Project Manager.Ready to lead complex environmental projects and drive sustainable solutions?.If you're a seasoned consultant who thrives on solving challenging environmental problems and building strong client relationships, this is your opportunity

Managing Consultant, Engineer/Geologist/Scientist Project Manager.Ready to lead complex environmental projects and drive sustainable solutions?.If you're a seasoned consultant who thrives on solving challenging environmental problems and building strong client relationships, this is your opportunity

Support environmental due diligence projects, including PhaseI Environmental Site Assessments, desktop reviews, environmental database reviews, site reconnaissance, and historical research. Skills / Experience Minimum Skills and Requirements: Bachelor’s degree in Environmental Engineering, Enviro

Rutgers University in The Ironbound seeks a Part-Time Instructor for the Fall 2026 semester in Political Science. Candidates should have a Bachelor's degree in political science or a related field, with an advanced degree preferred.

Part‑Time Instructor, Political Science, Fall 2026 The Department of Political Science, School of Arts and Sciences‑Newark, Rutgers University‑Newark (RU‑N), is hiring part‑time instructors for the Fall 2026 semester to teach political science surveys or upper‑level courses focused on sp

Similarly, for PSEG Long Island employees who accept job opportunities with PSEG or any of its subsidiaries (other than PSEG Long Island), their benefits would change and generally be consistent with other similarly situated new hires of that company. Special projects, such as leading all aspects of

Arcadis is seeking a Geologist/Environmental Scientist in Paramus, NJ.

Annually Date 02/2024 Location 1300 Airport Road, North Brunswick NJ Title Lead, Quality Control Chemist Department Quality Control Reports to Manager, Quality Control Laboratory FLSA (Exempt or Non-Exempt) Exempt Role Overview The Lead, QC Chemist performs specific routine analysis of

You will lead the design and synthesis of chemical systems and collaborate closely with various teams to translate scientific innovation into practical applications. This role demands a strong background in polymer chemistry and analytical science, focusing on innovative solutions in pharmaceuticals

The role requires a Bachelor’s degree in Chemistry or related field, and experience ranging from less than one year to one year in testing chemicals/pharmaceutical products.

The position involves teaching introductory courses and upper-level classes on topics like Congress and the presidency. Applicants must have a master’s degree in political science, and preference will be given to those with experience in International Relations or Comparative Politics.

Diese spannende Position erfordert eine Kombination aus Feldarbeit und Büroarbeit, einschließlich der Koordination von Boden- und Grundwassersampling sowie der Erstellung technischer Berichte.Sie werden die Möglichkeit haben, mit erfahrenen Fachleuten zusammenzuarbeiten und Ihre Fähigkeiten in e

Qualified candidates should hold a BS/MS in Chemistry and possess at least 5 years of lab experience with essential QC instruments. Lead, Quality Control Chemist to perform routine analysis in a regulated laboratory, ensuring compliance with specifications. The role involves supervising QC Chemists,

Education Requirements: Bachelor’s degree in a Scientific discipline is required (ideally Chemistry or Biochemistry). Responsibilities of the Assistant Chemist: Prepare laboratory samples according to established instructions and project specifications. Required Experience/Skills for the Assistant

VHB is seeking an emerging Environmental Engineer or Geologist/Hydrogeologist for our National Site Investigation & Remediation practice.

CDM Smith in New Jersey is seeking a geologist to plan and conduct geologic and environmental investigations, perform drilling and logging for complex projects, and log cores according to ASTM/USCS standards.

Role description Arcadis is seeking a Geologist or Scientist to join our Resilience Environment team in Paramus, New Jersey.

Job Description Date: 02/2024 Location: 1300 Airport Road, North Brunswick NJ Title: Lead, Quality Control Chemist Department: Quality Control Reports to: Manager, Quality Control Laboratory FLSA: Exempt Role Overview The Lead, QC Chemist performs specific routine analysis of samples of raw ma