Chemist jobs in Chula Vista, CaliforniaCreate job alerts

Job Description Quality Control Chemist - Simply Biotech OVERVIEW Are you looking for a new career opportunity with an exciting biotech company?! Then we have got the right team for you! In this role, you are responsible for the duties listed below. Immediate opening for a Quality Control Chemist in San Diego, CA who possesses: • Bachelor's degree in Chemistry, Biochemistry, or a related field, • 1+ years of cGMP lab experience; pharmaceutical or biotech experience preferred, • Experience with analytical instrumentation, including HPLC, GC, or related equipment FULL DESCRIPTION: We are seeking a Quality Control Chemist to perform testing on raw materials, in-process samples, and finished products within a compliant laboratory environment. This role is responsible for analytical testing, sample and solution preparation, accurate documentation, equipment calibration, laboratory cleanliness, and identifying potential quality issues. The ideal candidate will have a chemistry or biochemistry background, cGMP lab experience, strong technical documentation skills, and hands-on experience with analytical instrumentation. The selected candidate will be responsible for: • Performing analytical testing on raw materials, in-process samples, and finished products, • Using analytical instruments such as HPLC/UPLC, GC, MS, FTIR, LC/MS, and related equipment, • Preparing samples and solutions according to established methods, • Calibrating and maintaining laboratory equipment, • Documenting all work in compliance with cGMP requirements, • Identifying and reporting quality issues, • Supporting corrective actions as needed, • Assisting with SOP updates, • Maintaining laboratory cleanliness and organization, • Supporting a compliant laboratory environment, • Managing testing priorities accurately and efficiently, • Working both independently and as part of a team, • Following laboratory procedures, safety standards, and documentation requirements, • Performing other duties as assigned The selected candidate will also possess: • Bachelor's degree in Chemistry, Biochemistry, or a related field required, • 1+ years of cGMP laboratory experience required, • Pharmaceutical or biotech lab experience preferred, • Experience with analytical instrumentation required, • Experience with HPLC, GC, or related equipment preferred, • Experience with HPLC/UPLC, GC, MS, FTIR, or LC/MS preferred, • Strong attention to detail, • Strong technical documentation skills, • Ability to follow established laboratory methods and procedures, • Ability to identify and report potential quality issues, • Ability to manage priorities in a laboratory environment, • Ability to work independently and collaboratively on a team, • Ability to work onsite in San Diego, CA, • Ability to support a temporary-to-hire opportunity Physical Requirements: • Ability to sit, stand, walk, bend, reach, and move throughout the laboratory during the workday, • Ability to use hands and fingers for sample preparation, solution preparation, instrumentation, documentation, and computer work, • Ability to review laboratory data, test results, SOPs, batch records, and computer screens for extended periods, • Ability to work with laboratory equipment, analytical instruments, samples, reagents, and related materials, • Ability to occasionally lift, carry, or move standard laboratory supplies, samples, or equipment as needed, • Ability to work in a cGMP laboratory environment while following applicable safety, documentation, and quality procedures, • Ability to wear required personal protective equipment as needed Salary Range: $24 to $28/hour More information can be found at www.simplybiotech.com. Company DescriptionSimply Biotech was founded in 2008 and has been repeatedly recognized as one of San Diego County's fastest growing businesses. In 2025, we were named Business Journal's 'Best Places to Work'. Even as our competitors are scaling back and laying off staff, Simply Biotech is expanding to new markets and hiring additional staff in existing offices.Simply Biotech was founded in 2008 and has been repeatedly recognized as one of San Diego County's fastest growing businesses. In 2025, we were named Business Journal's 'Best Places to Work'. Even as our competitors are scaling back and laying off staff, Simply Biotech is expanding to new markets and hiring additional staff in existing offices.

Entity: Technology Job Family Group: Research & Technology Group Job Description: Job Description About us Our purpose is to bring together people, energy and markets to power and navigate a changing world. In a time of constant change and possibility we need new talent to pursue commercial opportunities, fueled by world-class insight and expertise. We’re always striving for more innovative digital solutions, sustainable outcomes and closer collaboration across our company and beyond, and you could be part of that too. Together we continue to grow as the world’s leading energy company! The Fuels and Low Carbon Technology (F&LCT) is a team of over 300 technologists, scientists and engineers who provide pioneering solutions to support bp’s Fuels, Refining, Bioenergy and Hydrogen businesses. We also support the Technology group through Innovation Management, Modelling, Digital Science and our academic research programs. The Bioenergy & Hydrogen Technology team (B&HT) will bring together scientists and engineers dedicated to delivering low carbon energy solutions that align with bp’s strategy while also supporting the technological needs of our oil and gas projects. The team works across many bp’s businesses supporting areas such as novel feedstocks, biogas and advanced biofuels. The opportunity The successful candidate will become part of a collaborative team of scientists and must demonstrate excellent communication, critical thinking, and problem-solving abilities, coupled with a keen enthusiasm for scientific discovery. Working closely with the analytical, fermentation, synthetic biology, and biochemistry teams, the Analytical Chemist will be responsible for sample preparation and analysis—including both large and small molecules—using advanced chromatographic and spectroscopic techniques. They will ensure meticulous maintenance of laboratory records, operate state-of-the-art analytical equipment, and effectively communicate results to team members. This hands-on role requires recent experience in independently delivering experimental outcomes, a strong interdisciplinary approach to problem-solving, and a commitment to maintaining safe, compliant laboratory practices while actively supporting a culture of HSSE excellence. Role Accountabilities Work safely and autonomously in a laboratory environment, maintaining strict adherence to HSSE requirements, standard operating procedures, and bp’s Code of Conduct. Rapidly adapt to new analytical techniques and protocols and contribute to the development, optimization, and validation of new analytical methods. Independently perform sample preparation and instrumental analysis using advanced chromatographic techniques, including liquid, gas, and ion chromatography coupled with mass spectrometry. Support multiple projects concurrently in a fast‑paced, multidisciplinary research environment, working both independently and as part of project teams. Evaluate data quality, interpret results, and clearly communicate scientific findings through well‑structured written reports and oral presentations. Maintain thorough, accurate experimental records and ensure data integrity and traceability. Essential Education and Experience Education Ph.D. in Analytical Chemistry, Chemistry, or Biochemistry with a minimum of 2 years of relevant experience, or M.S. in Analytical Chemistry, Chemistry, or Biochemistry with a minimum of 5 years of relevant experience, or B.S. in Analytical Chemistry, Chemistry, or Biochemistry with a minimum of 8 years of relevant experience. Experience and Required Qualifications Proven ability to work safely and independently within a laboratory setting. Advanced technical expertise in analytical techniques, particularly chromatography. Demonstrated experience developing and optimizing analytical methods for diverse analytes (e.g., small molecules, proteins, fermentation products) in complex matrices using UPLC, IC, and GC coupled with MS. Strong proficiency in generating, interpreting, and reporting high‑quality data within defined timelines. Demonstrated troubleshooting and problem‑solving skills with a high level of attention to detail. Effective communicator with the ability to anticipate project needs, estimate resource requirements, and collaborate across disciplines. Self‑motivated, highly organized, and capable of prioritizing tasks in a dynamic research environment. Desirable Criteria Hands‑on experience with Agilent instrumentation, including UHPLC, LC‑MS (QQQ, QTOF), micro‑GC, GC‑MS, ICP‑OES, and associated software (OpenLab CDS, MassHunter). Familiarity with Thermo IC‑MS instrumentation and Chromeleon software. Experience with Bruker FTIR instrumentation and Opus software. Familiarity with current proteomics and metabolomics workflows. Experience with compositional feedstock analysis techniques, including elemental analysis (ICP‑OES, CHNS). Familiarity with Benchling electronic lab notebook (ELN). Behaviors and Ways of Working Demonstrates strong “One Team” behaviors by supporting colleagues, fostering capability development, recognizing the contributions of others, and prioritizing team success. Exhibits strong “Respect” behaviors by valuing diverse perspectives, building trust through open communication, and contributing to an inclusive workplace environment. Maintains an excellent safety record and consistently follows complex standard operating procedures. Travel – up to 10%. Travel between the various locations (in the UK, US, Europe, India, and China) may be required. How much do we pay (Base)? (102,000.00 & 189,000.00 USD) *Note that the base pay range listed for this position is a good faith and reasonable estimate of the range of possible base compensation at the time of posting. We offer a reward and wellbeing package to enable your work to fit with your life. These can include, but are not limited to, access to health, vision and dental insurance, flexible working schedule, paid time off policy, discretionary annual bonus program, long-term incentive program, and a generous 401K matching program. You may learn more about our generous benefits at _. Why join bp: At bp, we support our people to learn and grow in a diverse and challenging environment. We believe that our team is strengthened by diversity. We are committed to encouraging an inclusive environment in which everyone is respected and treated fairly. There are many aspects of our employees’ lives that are meaningful, so we offer benefits to enable your work to fit with your life. These benefits can include flexible working options, a generous paid parental leave policy, and excellent retirement benefits, among others! Travel Requirement Up to 10% travel should be expected with this role Relocation Assistance: This role is not eligible for relocation Remote Type: This position is not available for remote working Skills: Agility core practices, Analytical Thinking, Bioprocess Design, Chemical kinetic modelling, Collaboration, Communication, Creativity and Innovation, Curiosity, Experimental Design, Industry technology knowledge, Intellectual Asset Management, Life cycle and circularity, Multi-physics modelling, New process technology scale-up, Novel process development, Pilot and demonstration plant operation, Presenting, Problem Solving, Process Safety Engineering, Science and Technology Leadership, Scientific publication, Talent Matching, Technoeconomic evaluation of processes, Thermophysical modelling, Thought Leadership Legal Disclaimer: We are an equal opportunity employer. We do not discriminate on the basis of protected characteristics like race, religion, color, sex, national origin, sexual orientation, veteran status or disability status. Individuals with an accessibility need may request an adjustment/accommodation related to bp’s recruiting process (e.g., accessing the job application, completing required assessments, participating in telephone screenings or interviews, etc.). If you would like to request an adjustment/accommodation related to the recruitment process, please _. If you are selected for a position and depending upon your role, your employment may be contingent upon adherence to local policy. This may include pre-placement drug screening, medical review of physical fitness for the role, and background checks.

Job DescriptionQC Chemist About the Role We are seeking a detail-oriented QC Chemist to join our Quality Control team in a GMP-regulated laboratory environment. In this role, you will perform analytical testing of raw materials, in-process samples, and finished products to ensure compliance with quality and regulatory standards. This is an excellent opportunity for a chemist with hands-on HPLC experience who enjoys working in a collaborative, science-driven environment and wants to expand their expertise across a variety of analytical techniques and instrumentation. Key Responsibilities • Perform routine and non-routine analytical testing using HPLC and other laboratory instrumentation., • Analyze raw materials, in-process samples, and finished products according to approved test methods., • Prepare samples, reagents, standards, and mobile phases for laboratory testing., • Accurately document analytical results and maintain laboratory records in compliance with GMP, SOPs, and data integrity requirements., • Calibrate, maintain, and troubleshoot laboratory equipment as needed., • Participate in laboratory investigations, deviations, and out-of-specification (OOS) activities., • Collaborate with cross-functional team members to support testing schedules and product release timelines., • Manage multiple analytical methods and instruments with a high degree of accuracy and attention to detail once fully trained.Required Qualifications, • Bachelor's degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, or a related scientific discipline., • Minimum of 2 years of experience in a Quality Control or analytical laboratory environment., • Hands-on experience operating and troubleshooting HPLC systems., • Experience preparing samples, interpreting analytical data, and documenting laboratory activities in a regulated setting., • Knowledge of GMP regulations, SOP compliance, data integrity principles, and quality standards., • Strong organizational skills with the ability to manage multiple priorities in a fast-paced laboratory environment., • Excellent attention to detail and commitment to producing high-quality results.Preferred Qualifications Experience with one or more of the following is highly desirable: • UPLC, • Gas Chromatography (GC), • USP Compendial Testing, • Elemental Analysis, • Mass Spectrometry (MS), • LC/MS, • FTIR, • Chromatography method execution and troubleshooting, • Pharmaceutical manufacturing or pharmaceutical quality systemsWork Environment, • 100% onsite laboratory-based position, • First Shift: Monday through Friday, 8:00 AM to 5:00 PM, • Collaborative team of approximately 8 laboratory professionals, • Structured onboarding, mentorship, and hands-on training program, • Opportunity to work independently once training and competency requirements are completed, • Occasional extended days may be required to support analytical testing and instrument run schedulesWhy this position?, • Gain exposure to a broad range of analytical techniques and instrumentation, • Work in a collaborative, team-oriented GMP laboratory, • Receive hands-on mentorship and professional development opportunities, • Contribute directly to product quality and regulatory compliance in a highly regulated industryJob Type & Location This is a Contract position based out of San Diego, CA. Pay and Benefits The pay range for this position is $24.00 - $28.00/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) Workplace Type This is a fully onsite position in San Diego,CA. Application Deadline This position is anticipated to close on Aug 3, 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 Production Process Chemist - Simply Biotech OVERVIEW Are you looking for a new career opportunity with an exciting biotech company?! Then we have got the right team for you! In this role, you are responsible for the duties listed below. Immediate opening for a Production Process Chemist in San Diego, CA who possesses: • Bachelor's degree in Chemistry, Biochemistry, or a related science field, • Strong organizational skills and attention to detail, • cGMP, peptide manufacturing, or batch support experience is a plus FULL DESCRIPTION: We are seeking a Production Process Chemist to support peptide manufacturing processes from technology transfer through commercial production. This 3-month temporary role will provide floor-side technical support, assist with investigations and troubleshooting, support equipment qualification, and contribute to process documentation, PPQ, and CPV activities. The ideal candidate will have a science background, strong organizational skills, and an interest in learning manufacturing processes, cGMP documentation, and batch support within a peptide manufacturing environment. The selected candidate will be responsible for: • Providing floor-side technical support during peptide manufacturing operations, including SPPS, cleavage, purification, and lyophilization, • Assisting with investigations and troubleshooting of critical manufacturing issues, • Collecting data and performing technical assessments, • Supporting deviation investigations, root cause analysis, and CAPA implementation, • Supporting technology transfers between Process Development and Manufacturing, as well as across manufacturing sites, • Helping ensure strong process understanding, reproducibility, and complete GMP documentation during transfer and production activities, • Assisting with Process Performance Qualification activities, including protocol execution support, data collection, data review, and reporting, • Supporting Continued Process Verification through process monitoring, trend analysis, and identification of potential process variability, • Supporting qualification of new manufacturing equipment, including IQ, OQ, and PQ protocol execution, • Preparing and maintaining related GMP documentation, • Helping improve manufacturing workflows and batch documentation to reduce human error, strengthen data integrity, and improve operational consistency, • Collaborating cross-functionally with Manufacturing, Process Development, Quality Control, and Quality Assurance, • Supporting routine operations, investigations, and new production introductions, • Learning and supporting peptide manufacturing processes, paperwork, and batch-related documentation as needed The selected candidate will also possess: • Bachelor's degree in Chemistry, Biochemistry, or a related field required, • Minimum of 1 year of experience in pharmaceutical manufacturing or a cGMP environment preferred, • Peptide manufacturing experience preferred, • Foundational understanding of cGMP manufacturing principles, • Familiarity with peptide manufacturing processes, including SPPS, cleavage, purification, and lyophilization preferred, • Familiarity with equipment qualification, including IQ, OQ, and PQ preferred, • Hands-on exposure to process validation activities, including PPQ execution and CPV support, preferred, • Understanding of cleaning validation principles, residue risk assessment, and contamination control preferred, • Familiarity with quality systems, including deviations, investigations, CAPAs, and change controls, • Strong verbal and written communication skills, • Ability to communicate technical information clearly to operators, peers, and cross-functional partners, • Hands-on, proactive mindset with willingness to work directly on the manufacturing floor, • Developing problem-solving and troubleshooting skills, • Ability to collaborate effectively across Manufacturing, Process Development, Quality Control, and Quality Assurance, • Strong attention to detail and commitment to compliance, data integrity, and operational excellence, • Ability to balance process robustness, compliance, and manufacturing efficiency, • Ability to work onsite in San Diego, CA, • Ability to work a temporary 3-month assignment, • Ability to work Monday through Friday, 8:00 AM to 5:00 PM or 7:30 AM to 4:30 PM Physical Requirements: • Ability to sit, stand, and walk throughout the workday, including time on the manufacturing floor, • Ability to use hands and fingers for documentation, computer work, data entry, and handling materials or equipment as needed, • Ability to review batch records, GMP documentation, technical data, reports, and computer screens for extended periods, • Ability to communicate by phone, email, video meeting, and in person throughout the workday, • Ability to occasionally bend, reach, lift, carry, or move standard laboratory, manufacturing, or office materials as needed, • Ability to work in a cGMP manufacturing environment while following applicable safety, gowning, documentation, and quality procedures, • Ability to wear required personal protective equipment as needed for manufacturing or production floor support Salary Range: $28 to $30/hour More information can be found at www.simplybiotech.com. Company DescriptionSimply Biotech was founded in 2008 and has been repeatedly recognized as one of San Diego County's fastest growing businesses. In 2025, we were named Business Journal's 'Best Places to Work'. Even as our competitors are scaling back and laying off staff, Simply Biotech is expanding to new markets and hiring additional staff in existing offices.Simply Biotech was founded in 2008 and has been repeatedly recognized as one of San Diego County's fastest growing businesses. In 2025, we were named Business Journal's 'Best Places to Work'. Even as our competitors are scaling back and laying off staff, Simply Biotech is expanding to new markets and hiring additional staff in existing offices.

Job Description Beloteca, Inc. is a generic pharmaceutical development company specializing in the development of injectable products. It is desirable that the candidate have past practical experience and education in handling chemicals, operating laboratory equipment, generating and manipulating data, as well as computer database and word-processing skills. Job Description: • Independent execution of various standard laboratory techniques, including but not limited to H/UPLC, GC, water content analysis per USP, appearance assessment, water activity per USP, • May participate in qualification/verification of assays, • Assay and documentation review and report writing, • Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices., • Execution of more advanced analytical techniques with assistance such as LC/MS, DSC, and TGA, • Independent preparation of samples, solutions, instrument set-up and breakdown, • Independent preparation of data packets and creation of stability data sheets and Certificates of Analysis to summarize analytical testing, • Assisted participation in Out of Specification investigations and the documentation of analytical deviations along with Qualified Investigators and management, • Understand and apply ICH and FDA guidance Basic Qualifications: • BS in Biology, Chemistry and/or related science discipline., • Computer literacy in Windows applications and the MS Office., • Excellent oral and written communication skills are essential., • Minimum of 3 years experience with HPLC, UPLC, GC, Karl Fisher, pH, • Maintain a safe working environment for all employees, ensuring compliance to all local, state, and federal codes and regulations. Preferred Qualifications: • Ability and willingness to work flexible hours., • Great attention to detail, quality, and a desire for success., • Self-motivated individual with the ability to learn, lead and strengthen the Beloteca, Inc. team.

Job DescriptionProduction Process Chemist (Contract) | Peptide Manufacturing & GMP OperationsOverview We are seeking a Production Process Chemist to provide hands-on technical support for commercial peptide manufacturing operations within a regulated biotechnology environment. This is an excellent opportunity for a chemist or process professional looking to gain extensive exposure to GMP manufacturing, process validation, technology transfer, equipment qualification, and commercial-scale peptide production. In this highly collaborative role, you will partner with Manufacturing, Process Development, Quality Control, and Quality Assurance teams to support production activities, troubleshoot manufacturing challenges, investigate deviations, and ensure compliance with cGMP standards. The ideal candidate is technically strong, detail-oriented, and thrives in a fast-paced manufacturing environment. Key Responsibilities • Provide floor-side technical support for commercial peptide manufacturing operations, including:, • Solid-Phase Peptide Synthesis (SPPS), • Peptide cleavage, • Purification processes, • Lyophilization (freeze drying), • Partner with Manufacturing, Process Development, QA, and QC teams to support routine production and continuous improvement initiatives., • Support technology transfer activities to successfully implement new and optimized manufacturing processes., • Assist with deviation investigations, root cause analysis, and quality system documentation., • Support CAPA (Corrective and Preventive Action) activities through data collection, analysis, and documentation., • Execute and document process validation activities, including:, • Process Performance Qualification (PPQ), • Continued Process Verification (CPV), • Support equipment qualification activities, including:, • Installation Qualification (IQ), • Operational Qualification (OQ), • Performance Qualification (PQ), • Monitor manufacturing processes, analyze production trends, and identify opportunities for process improvements., • Review batch records and manufacturing documentation to ensure accuracy, completeness, and cGMP compliance.Required Qualifications, • Bachelor’s degree in Chemistry, Biochemistry, Chemical Engineering, Bioengineering, or a related scientific discipline., • Experience working in a cGMP-regulated pharmaceutical, biotechnology, or life sciences manufacturing environment., • Knowledge of peptide manufacturing processes, including:, • Solid-Phase Peptide Synthesis (SPPS), • Purification, • Cleavage, • Lyophilization, • Experience supporting process validation activities such as PPQ and CPV., • Experience supporting equipment qualification activities including IQ, OQ, and PQ., • Understanding of deviation investigations, root cause analysis, and quality systems., • Experience supporting CAPA programs and documentation., • Strong technical writing and GMP documentation skills., • Excellent troubleshooting, analytical, and problem-solving abilities., • Strong communication skills and ability to work cross-functionally., • Willingness to spend significant time supporting operations on the manufacturing floor.Preferred Qualifications, • Prior peptide manufacturing experience., • Experience supporting commercial pharmaceutical or biotechnology manufacturing operations., • Familiarity with technology transfer projects., • Experience working within formal quality systems and regulatory environments., • Demonstrated ability to manage multiple priorities in a fast-paced production setting.Job Type & Location This is a Contract position based out of San Diego, CA. Pay and Benefits The pay range for this position is $28.00 - $33.00/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) Workplace Type This is a fully onsite position in San Diego,CA. Application Deadline This position is anticipated to close on Aug 3, 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.

About Mercor projects** Experts in our network contribute to: - Training and evaluating AI models in Chemistry - Creating tasks and deliverables based on real-world scenarios - Providing domain-specific feedback to advance frontier AI research Projects vary in scope and duration, with typical commit

Hours: Shift Start Time: 6 PM Shift End Time: 2:30 AM AWS Hours Requirement: 8/40 - 8 Hour Shift Additional Shift Information: Weekend Requirements: Every Other On-Call Required: No Hourly Pay Range (Minimum - Midpoint - Maximum): $49.700 - $64.130 - $71.820 The stated pay scale reflects the range that Sharp reasonably expects to pay for this position. The actual pay rate and pay grade for this position will be dependent on a variety of factors, including an applicant's years of experience, unique skills and abilities, education, alignment with similar internal candidates, marketplace factors, other requirements for the position, and employer business practices. • Other Education required for CA State CLS or CLS specialty., • California Clinical Laboratory Scientist (CLS) Generalist license - CA Department of Public Health OR California Clinical Chemist Scientist License - CA Department of Public Health OR California Clinical Microbiologist Scientist License - CA Department of Public Health OR California Clinical Toxicologist Scientist License - CA Department of Public Health OR California Clinical Genetic Molecular Biologist Scientist License - CA Department of Public Health OR California Clinical Cytogeneticist Scientist License - CA Department of Public Health OR California Clinical Histocompatability Scientist License - CA Department of Public Health -REQUIRED, • Experience in a clinical laboratory as a CLS., • The CLS license must be respective to the department's assigned area. ASCP preferred., • Analytical Testing ProceduresCompletes testing procedures using written policies, procedures and other appropriate resources; identifies issues in and submits necessary revisions to policies and procedures.Performs new procedures and policies within acceptable training time intervals; meets/exceeds department turnaround time goals.Documents activities and results consistently, thoroughly and legibly; proof reads and double checks own work to achieve zero defects and zero harm.Reviews operational reports for possible clerical and analytical errors and make correction as necessary.Evaluates data for accuracy and verifies any questionable finding with thorough investigation and appropriate follow-through.Performs pre-analytical (patient reception, sample collection, processing) and analytical procedures and demonstrates assessment of testing factors with regard to patient age and population specific groups.Demonstrates emotional intelligence, critical thinking and logical decision making, especially under critical and stressful situations to reach acceptable resolutions.Acts as a key resource for employee/student training, development and competency assessment.Act as a key operator for testing, validation, analyzers and technology.Performs additional duties to meet operational needs.Participates in writing and revision of policies and procedures., • Equipment ManagementUtilizes equipment (including phone, copier, fax, printer, etc.,) analyzers, products, and other tools per manufacturer's and training instructions and according to established procedures; facilitates issue resolution.Reports, documents and resolves or facilitates resolution of equipment/analyzers/tool/reagent issues and failures in a timely and efficient manner.Removes defective equipment/analyzers from use, documents problem, and notifies appropriate personnel for repair; verifies equipment/analyzers inspections are up-to-date. Follows through on problem resolution and validates equipment/analyzers performance post repair.Participates in analyzer and test methodology, evaluation and selection and provides input in decision making processes.Demonstrates competency and efficient use of tool applications (IS, PC, other system/software) and equipment to produce the end product.Performs and validates required preventive and corrective maintenance on equipment/analyzers/tools.Actively manages inventory and demonstrates ability to evaluate consumables (reagent/supply) inventory to prevent shortages; alerts ordering personnel., • Quality AssuranceCoordinates and completes processes to meet standards established to maintain quality testing, including collaboration and engagement in continuous improvement of processes.Represent laboratory department in entity or system committees, taskforces, or workgroups as necessary.Communicates clearly using tools Closed Loop and SBAR.Supervises work activities performed by Medical Lab Technicians, Certified Phlebotomy Technicians and Laboratory Assistants, and promotes accountability, mutual respect and teamwork.Completes and assesses QC performance, proficiency testing, test validation/calibration/linearity with indicated corrective action and resolution as needed.Has knowledge of and reviews quality assurance indicators and monitors and works with the laboratory team to meet/exceed the established thresholds.Completes and validates daily position tasks within expected timeframes to meet QA indicator goal expectations.Identifies errors and follows-through with investigation, correction, documentation, and notification to appropriate caregiver and lab leadership.Demonstrates process of self-discovery, including knowledge of strengths and weaknesses and views deficiencies as opportunities for growth; sets goals for self-improvement.Performs shift lead duties as necessary.Receives feedback well and provides thoughtful feedback to others.Participates in regulatory and safety compliance activities as assigned. Sharp HealthCare is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability or any other protected class.

Hours: Variable AWS Hours Requirement: 8/40 - 8 Hour Shift Weekend Requirements: As Needed On-Call Required: No Hourly Pay Range (Minimum - Midpoint - Maximum): $67.070 - $86.540 - $96.930 The stated pay scale reflects the range that Sharp reasonably expects to pay for this position. The actual pay rate and pay grade for this position will be dependent on a variety of factors, including an applicant's years of experience, unique skills and abilities, education, alignment with similar internal candidates, marketplace factors, other requirements for the position, and employer business practices. Provides the technical knowledge, expertise and judgment required to support the Sharp HealthCare (SHC) mission and scope of laboratory services. • Bachelor's Degree in related field of study., • 5 Years full time equivalent experience in a clinical lab., • California Clinical Laboratory Scientist (CLS) Generalist license - CA Department of Public Health -REQUIRED, • California Clinical Chemist Scientist License - CA Department of Public Health -REQUIRED, • California Clinical Microbiologist Scientist License - CA Department of Public Health -REQUIRED, • California Clinical Toxicologist Scientist License - CA Department of Public Health -REQUIRED, • California Clinical Genetic Molecular Biologist Scientist License - CA Department of Public Health -REQUIRED, • California Clinical Cytogeneticist Scientist License - CA Department of Public Health -REQUIRED, • California Clinical Histocompatability Scientist License - CA Department of Public Health -REQUIRED, • Pathologist Assistant PA(ASCP) - ASCP Board of Certification -REQUIRED, • Other Education required for CA State CLS or CLS specialty., • The limited CLS license specialty must be respective to the department's assigned area. ASCP preferred., • Communication and Teamwork: Proactively initiates communication and works cooperatively with others to successfully complete work assignments. Demonstrates positive verbal and non-verbal communication skills. Completes documentation legibly, accurately, and timely. Stays informed through staff meetings, electronic communication, in-services, and educational opportunities. Establishes effective working relationships between internal and external customers. Seeks opportunities for feedback to improve effectiveness of own communication. Validates messages by clarifying expectations and verifying understanding of agreements/action plans., • Demonstrates Flexibility and Adaptability: Uses time effectively and actively sets priorities. Demonstrates flexibility in work practices and adjusts to unscheduled situations. Cooperates with initiatives to improve work processes. Tries new ideas and new ways of doing things. Positively embraces and is receptive to change and actively participates in the process., • Equipment Use, Testing and Documentation: Supervises and uses equipment and related applications in completing testing and documentation processes. Utilizes all equipment (including phone, copier, fax, etc.), instruments, products, and other tools per manufacturer's and training instructions and according to established procedures. Demonstrates competency and efficient use of all tool applications (IS, PC, other system/software) and equipment to produce the end product. Performs required preventive and corrective maintenance on equipment/tools. Reports and documents equipment/tool/reagent issues and failures. Checks inventory expiration dates and demonstrates ability to evaluate consumables (reagent/supply) inventory to prevent shortages; alerts ordering personnel. Removes defective equipment from use, documents problem, and notifies appropriate personnel for repair; verifies equipment inspections are up-to-date., • Leadership: Collaborates with and advises directors, managers, leads and section staff in maintaining and enhancing technical, managerial, and financial performances. Assists in the development and enhancement of pathology services through collaboration with patient care and support services to provide optimal patient care. Develops and institutes policies and procedures to facilitate application of SHC corporate commitment to compliance guidelines. Acts as Technical Consultant regarding abnormal or unusual orders or results: interacts with staff and physicians to solve problems and provide interpretation of lab procedures and processes; may include oversight of near patient testing; performs technical lead duties. Apprises Senior Specialists, Lab Managers or Pathologists of conditions or situations that may be or are compromising quality of care. Supports and provides input for development, revisions, and implementation of policies and procedures to provide consistent quality lab services to all customers; participates in annual review of policies and procedures. Conducts regularly scheduled section meetings providing updates and communication to assigned staff; holds 4-5 section meetings and directs at least 6 subgroup meetings annually. Performs or provides input for performance appraisals and corrective action of assigned staff to Senior Specialists or Lab Manager/Director; completes performance appraisals within 30 days of anniversary date. Conducts or facilitates core and technical competency assessment of all assigned staff members. Adjusts for changes in workload and shifting of staff and skill mix; makes recommendations for staff utilization, development, and section process optimization. Reviews patient results with appropriate actions or coaching of staff when problems are found; assists Senior Specialist or Lab Manager with personnel problem solving activities; including documentation and coaching with resolution, follow through, and prevention. Assists in maintaining CAP, JCAHO, CA state, AABB, FDA, and other accreditation and regulatory agency standards and regulations. Demonstrates emotional intelligence, critical thinking, and logical decision-making, especially under critical and stressful situations, to reach acceptable resolutions., • Test processes by evaluating quality control systems, data and outcomes: Supervises and performs pre-analytical, analytical, and post-analytical tests and processes by evaluating quality control systems, data, and outcomes. Completes and assesses all QC procedures in place with indicated corrective action and resolution as needed. Coordinates and completes processes in place to meet standards established to maintain quality testing. Has knowledge of and reviews quality assurance indicators and monitors in place and works with the laboratory team to meet the established thresholds. Completes daily position tasks within expected timeframes to meet QA indicator goal expectations. Identifies errors and follows-through with investigation, correction, documentation, and notification to appropriate caregiver and lab leadership., • Test processes relative to diagnosis, assessment and treatment: Supervises and performs pre-analytical, analytical and post-analytical test processes and evaluates results produced relative to the diagnosis, assessment, and treatment of disease. Completes testing processes without error using written policies, procedures and other appropriate resources; identifies issues in policies or procedures. SHC corporate commitment to compliance training principles are correctly and appropriately utilized when performing assigned procedures as written. Performs new procedures and policies within acceptable training time intervals; meets department turnaround time goals. Documents activities and results consistently, thoroughly and legibly; proofreads and double checks own work to minimize errors. Evaluates data for accuracy and verifies any questionable finding with thorough investigation and appropriate follow-through. Supervises and performs pre-analytical (patient reception, sample collection, processing) and analytical procedures and demonstrates assessment of testing factors with regard to patient age and population specific groups. Sharp HealthCare is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability or any other protected class.

Hours: Shift Start Time: Variable Shift End Time: Variable AWS Hours Requirement: 8/40 - 8 Hour Shift Additional Shift Information: Weekend Requirements: As Needed On-Call Required: No Hourly Pay Range (Minimum - Midpoint - Maximum): $57.740 - $74.490 - $83.440 The stated pay scale reflects the range that Sharp reasonably expects to pay for this position. The actual pay rate and pay grade for this position will be dependent on a variety of factors, including an applicant's years of experience, unique skills and abilities, education, alignment with similar internal candidates, marketplace factors, other requirements for the position, and employer business practices. Provides the technical knowledge, expertise and judgment required to support the Sharp HealthCare (SHC) mission and scope of laboratory services. • Other: Education required for CA State CLS., • 5 Years experience in a Clinical Laboratory as a CLS required; including competency and expertise in one or more clinical departments., • California Clinical Laboratory Scientist (CLS) Generalist license - CA Department of Public Health OR California Clinical Chemist Scientist License - CA Department of Public Health OR California Clinical Microbiologist Scientist License - CA Department of Public Health OR California Clinical Toxicologist Scientist License - CA Department of Public Health OR California Clinical Histocompatability Scientist License - CA Department of Public Health OR California Clinical Genetic Molecular Biologist Scientist License - CA Department of Public Health OR California Clinical Cytogeneticist Scientist License - CA Department of Public Health -REQUIRED, • The CLS license must be respective to the department's assigned area. ASCP Specialty Certification preferred (SC, SH, SM, SBB, SCYM)., • Communication and Teamwork: Proactively initiates communication and works cooperatively with others to successfully complete work assignments. Demonstrates positive verbal and non-verbal communication skills. Completes documentation legibly, accurately, and timely. Stays informed through staff meetings, electronic communication, in-services, and educational opportunities. Establishes effective working relationships between internal and external customers. Seeks opportunities for feedback to improve effectiveness of own communication. Validates messages by clarifying expectations and verifying understanding of agreements/action plans and utilizing communication tools, such as Closed Loop and SBAR., • Demonstrates flexibility and Adaptability: Uses time effectively and actively sets priorities. Demonstrates flexibility in work practices and adjusts to unscheduled situations. Cooperates with initiatives to improve work processes. Tries new ideas and new ways of doing things. Positively embraces and is receptive to change and actively participates in the process., • Equipment Use, Testing and Documentation: Utilizes all equipment (including phone, copier, fax, etc.), instruments, products, and other tools per manufacturer's and training instructions and according to established procedures; facilitates issue resolution. Reports, documents and resolves or facilitates resolution of equipment/analyzers/tool/reagent issues and failures in a timely and efficient manner. Removes defective equipment from use, documents problem, and notifies appropriate personnel for repair; verifies equipment inspections are up-to-date. Follows through on problem resolution and validates equipment/analyzers performance post repair. Participates in analyzer and test methodology, evaluation, selection and validation, and provides input in decision-making processes. Demonstrates competency and efficient use of all tool applications (IT, PC, other system/software) and equipment to produce the end product. Demonstrates advanced competency of current software applications, including troubleshooting middleware issues, validating Auto-verification criteria, and working with vendor and IT to resolve software issues. Performs required preventive and corrective maintenance on equipment/analyzers/tools, including comprehensive validation of accuracy, complete documentation of work orders/issues and scheduled review of data/logs/reports as required by CLIA, CA State, CAP and other regulatory agencies. Actively manages inventory and demonstrates ability to evaluate consumables (reagent/supply) inventory to prevent shortages; alerts ordering personnel and proactively resolves immediate issues/shortages. With lab leadership approval, works with vendors to make appropriate changes to standing orders to meet business needs. Supervises and uses equipment and related applications in completing testing and documentation processes., • Leadership: Collaborates with and advises Directors, Managers, Sr. Specialists, Leads and section staff in maintaining and enhancing technical, managerial, and financial performances. Assists in the development and enhancement of laboratory services through collaboration with patient care and support services to provide optimal patient care. Develops and institutes policies and procedures to facilitate application of SHC corporate commitment to compliance guidelines. Acts as Technical Consultant regarding abnormal or unusual orders or results: interacts with staff and physicians to solve problems and provide interpretation of lab procedures and processes; may include oversight of near patient testing; performs technical lead duties. Apprises Senior Specialists, Lab Managers or Pathologists of conditions or situations that may be or are compromising quality of care. Supports and provides input for development, revisions, and implementation of policies and procedures to provide consistent quality lab services to all customers; participates in annual review of policies and procedures. Conducts regularly scheduled section meetings/huddles providing updates and communication to assigned staff; holds 4-5 section meetings and directs at least 6 subgroup meetings annually. Performs or provides input for performance appraisals and corrective action of assigned staff to Lab Manager/Director; completes performance appraisals within 30 days of anniversary date. Conducts or facilitates core and technical competency development and assessment of all assigned staff members. Adjusts for changes in workload and shifting of staff and skill mix; makes recommendations for staff utilization, development, and section process optimization. Reviews patient results with appropriate actions or coaching of staff when problems are found; assists Lab Manager/Director with personnel problem solving activities; including documentation and coaching with resolution, follow through, and prevention. Assists in maintaining CAP, JCAHO, CA State, AABB, FDA, and other accreditation and regulatory agency standards and regulations. Demonstrates emotional intelligence, critical thinking, and logical decision-making, especially under critical and stressful situations, to reach acceptable resolutions., • Test Processes by evaluating quality control systems, data and outcomes: Supervises and performs pre-analytical, analytical, and post-analytical tests and processes by evaluating quality control systems, data, and outcomes. Completes and assesses QC performance, proficiency testing, test validation/calibration/linearity with indicated corrective action and resolution as needed, including scheduled review. Coordinates and completes processes to meet standards established to maintain quality testing, including collaboration and engagement in continuous improvement of processes. Has knowledge of and reviews and monitors compliance of quality assurance indicators; works with the laboratory team to meet/exceed the established thresholds. Maintains expected goals and implements action plans as needed. Completes, validates and monitors daily position tasks within expected timeframes to meet QA indicator goal expectations. Identifies errors and follows-through with investigation, correction, documentation, coaching and notification to appropriate caregiver and lab leadership., • Test Processes relative to diagnosis, assessment and treatment: Supervises and performs pre-analytical, analytical and post-analytical test processes and evaluates results produced relative to the diagnosis, assessment, and treatment of disease. SHC corporate commitments to compliance training principles are correctly and appropriately utilized when performing assigned procedures as written. Completes testing procedures without error using written policies, procedures and other appropriate resources; identifies issues in and submits necessary revisions to policies and procedures. Performs new procedures and policies within acceptable training time intervals; meets/exceeds department turnaround time goals. Documents activities and results consistently, thoroughly and legibly; proof reads and double checks work in assigned section to achieve zero defects and zero harm. Reviews operational reports for possible clerical and analytical errors and make correction as necessary. Evaluates data for accuracy and verifies any questionable finding with thorough investigation and appropriate follow-through. Supervises and performs pre-analytical (patient reception, sample collection, processing) and analytical procedures and demonstrates assessment of testing factors with regard to patient age and population specific groups. Sharp HealthCare is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability or any other protected class.

Product Testers are wanted to work from home nationwide in the US to fulfill upcoming contracts with national and international companies.We guarantee 15-25 hours per week with an hourly pay of between $25/hr.There is no payment required in order to apply or to work as an In-Home Usage Tester.You do

Compensation: $45–$90 per completed task.The Consumer Insights Division of our organization is expanding its nationwide research team.We are seeking dependable individuals to support ongoing studies that influence the development of products, services, and digital experiences used across the Unite

Ultimate Staffing - - Responsibilities: Locate and pull items from shelves based on picking sheets; Pack orders securely with proper cushioning and shipping labels; Update inventory systems and maintain accurate stock counts; Operate equipment such as forklifts and pallet jacks safely; Load and unl

At IKEA, a warehouse job is so much more than moving products from A to B.It's your chance to make a positive impact, grow your skills, and help create a better everyday life for the many.What You'll Be Doing Day To Day.Contributing to the fulfillment of customer orders in different sales channels i

Kellermeyer Bergensons Services - 6971 Otay Mesa Road - Responsibilities: Cleaning restrooms, break areas (indoor/outdoor), office areas; Sweeping, mopping, dusting, removing trash; Ensure all walkways are clean and tidy at all times; Clean totes and other items; Some deep cleaning, as needed.

Paradies Lagardere Warehouse Associate.Our San Diego International Airport is now hiring for a Warehouse Associate, Full Time.Valid driver license with clean driving record - Mandatory.Great Reasons to Work with Us:.Career Advancement Opportunities.Medical Benefits (for full time positions).Associat

Scripps Research encompasses two elite and highly innovative institutes, the Calibr-Skaggs Institute for Innovative Medicines and Scripps Research Translational Institute, which merge foundational studies in biology, chemistry and computer science with translational science to produce pioneering dru

Labcorp is seeking an entry level Medical Lab Technician to join our team in San Diego, CA.Work Schedule: 1st shift: This is a casual/per diem position; hours will be "as needed" the start and end times will vary Job Responsibilities * Determine the acceptability of specimens for testing according

Labcorp is seeking an entry level Medical Lab Technician to join our team in San Diego, CA.Work Schedule: Tuesday - Saturday 6:00am - 2:30pm with rotating weekend.Job Responsibilities Determine the acceptability of specimens for testing according to established criteria Perform routine and complex t

Join to apply for the Medical Lab Technician (MLT) - Per Diem role at Labcorp.Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge or start your career in Clinical Lab Science? If so, Labcorp wants to speak with you about exciting opportunities as a Technici

Benefits We Offer: Comprehensive health, prescription, dental, vision, life, and disability plans Competitive pay rates Referral opportunities ? Refer a friend & Cash in! Travel reimbursement and per diem allowances Employee discounts Educational opportunities Health Advocates Network was fou

Research Administrative Assistant.Venesco, LLC is looking for a Research Administrative Assistant to support the Naval Health Research Center in San Diego, CA.The Research Administrative Assistant will be primarily responsible for providing administrative support and administrative functions includi

This position is open until filled with an initial application review to take place after June 22, 2026.Candidates are hired as a Nutrition Services Assistant at $19.The candidate will be trained to become a WIC Nutrition Assistant within 1 year of employment.Click here for California Department of

America is seeking an entry level Medical Lab Technician in San Diego, CA.This role involves determining the acceptability of specimens, performing routine technical procedures, and ensuring accurate test results to deliver quality patient care.Qualifications include an Associate’s degree in a rel

Overview Join to apply for the Medical Lab Technician (MLT) role at Labcorp.Labcorp invites qualified candidates to join our Core Lab in San Diego, CA.In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our mission: “Improving Health

Performs clinical laboratory test procedures in a manner that provides timely and accurate meaningful results in Hematology, Urinalysis, Chemistry, and coagulation testing. Technical Knowledge and Skills Required to Perform the Job: Familiarity and experience working with various laboratory instrum

Assistant Research Administrator.The USC Keck School of Medicine - Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California is an academic institute comprised of an expert panel of scientific collaborators committed to advancing the development of new treatments for Alzheime

The salary range for this position is $17.Under immediate supervision, the Admin Support Assistant performs general office support work of moderate and routine difficulty.Assignments are narrow in scope and may involve completing a component of a project; may assist in training new staff members; de

Labcorp in San Diego, CA is seeking a Technician to join our team.You will determine specimen acceptability, perform routine and complex tests, monitor and troubleshoot instruments, and report results to support patient care.Minimum qualifications include an Associate’s degree in a Chemical or Bio

Ideal candidates should have a Bachelor's degree in Chemistry, Biochemistry, Biology, Organic Chemistry, or a related scientific discipline. Bachelor's degree in Chemistry, Biochemistry, Biology, Organic Chemistry, or a related scientific discipline.

Murata Electronics in San Diego is looking for a Senior Technician, RF Test Engineering to maintain laboratory readiness and ensure proper calibration of test equipment.The ideal candidate will have at least 8 years of experience in RF product development, strong troubleshooting skills, and the abil

The USC Keck School of Medicine - Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California is an academic institute comprised of an expert panel of scientific collaborators committed to advancing the development of new treatments for Alzheimer’s Disease (AD) through innova

Warehouse Associate/ Backroom Processor-Point Loma Store.Job Category: Warehouse - all positions Requisition Number: WAREH020880.Full-Time On-site SD Point Loma Store 16 San Diego, CA 92110, USA.The Salvation Army Mission Statement.The Salvation Army, an international movement, is an evangelical par

Our Transmission Planning and Power Systems Analysis team works with a diverse mix of clients—investor-owned utilities, public power entities, developers, and ISOs/RTOs—to deliver smart, resilient, and future‑ready electric grid solutions.As part of Burns & McDonnell, we bring together decades

Eligibilities & Qualifications.Eligibilities & Qualifications.

Take the next step in your career as our new Costco Warehouse Associate to gain knowledge of company offerings to better serve clients, provide excellent service to customers and team members, and follow safety procedures and company policies.Other duties include adapt to shifting priorities and bus

We are seeking reliable and hardworking individuals to join our Event Set-Up Crew.In this role, you will be responsible for assembling, installing, and dismantling canopies, tents, stages, and other event structures.You will work as part of a team to ensure each event is set up safely, efficiently,

Help us succeed as our next Walmart Warehouse Associate to provide excellent service to customers and team members, gain knowledge of company offerings to better serve clients, and adapt to shifting priorities and business needs.Other duties include assist with organizing, stocking, and general upke

Odyssey is looking for a Research Associate to support the Traumatic Brain Injury Center of Excellence (TBICoE), to support the execution of clinical research efforts under the supervision of the project lead(s).In this role, you will participate in aspects of research including but not limited to r

Gexpro Services is a world-class Supply Chain Services outsource provider, specializing in developing and managing production inventory management programs.Our managed inventory programs are designed to support manufacturing OEM's with their engineered production material specifications, fulfillment