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Job DescriptionCompany Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Job Description Eurofins Lancaster Laboratories, a nationally recognized laboratory, is searching for a GMP Chemist in our Professional Scientific Services group in Foster City, CA. QC Chemist Responsibilities: • Support the qualification and requalification of Reference Standards through analytical testing techniques such as Appearance testing, FTIR, NMR, Liquid Chromatography (LC/HPLC/UPLC), TGA, DSC, and Karl Fischer titration, including performing correction factor calculations., • Ensure adherence to GMP regulations by completing required training, following Standard Operating Procedures (SOPs), and maintaining compliance-related documentation., • Review and verify laboratory documentation, calculations, and test preparations before sample analysis to help prevent deviations and laboratory investigations., • Perform data analysis and troubleshoot methods and instrumentation., • Prepare data for presentations and assist in generating technical reports, • Coordinate sample shipments and testing activities with external contract laboratories, and accurately document and upload analytical results into internal databases., • Work closely with cross-functional teams and external vendors, contract laboratories, and partners to support operational goals., • Initiate and perform investigations, as needed, • Write protocols and technical reports and transfer methods internally and externally, • Contribute to a safe, organized, and compliant laboratory environment by participating in routine housekeeping and weekly laboratory cleanup activities.Qualifications The Ideal Candidate would possess: • Demonstrated success in executing small molecule analytical chemistry methods adhering to SOPs and GMP guidelines., • At least 1 year of continuous experience in GMP/ GLP regulated environment., • Previous experience conducting and analyzing data for analytical methods such as UPLC/HPLC, FTIR, NMR, Thermogravimetric DSC/TGA, and KF titrations., • Understanding of experimentation and data analysis using Empower software (Version III), • Excellent written and verbal communication skills and experience interacting with people from a wide range of skill levels and experience, • Ability to communicate complex scientific findings and recommendations in one-on-one discussions and departmental meetings, • Excellent technical writing experience such as protocols, reports, and SOPs, • Demonstrated ability to work as an independent, self-motivated, detail-oriented, result-driven and highly flexible team-player in a fast-paced working environment, • Strong computer, scientific, and organizational skills, • Demonstrated exceptional attention to detail and strong project management capabilities, effectively managing project resources, including materials, personnel, and timelines, while proactively identifying and escalating critical issues to project leadership and management., • Ability to work independently and as part of a team with internal and external clients, self‑motivation, adaptability, and a positive attitude, • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Qualifications • B.S. in Chemistry or related scientific field and minimum of 4-5 years of experience in an analytical environment, or M.S. degree and 1-3 years of experience, • Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information • Excellent full time benefits including comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match, • Paid vacation and holidays Eurofins Lancaster Laboratories Professional Scientific Services® (PSS) is a global, award-winning insourcing solution that places our people at our clients’ site dedicated to running and managing laboratory services while eliminating headcount, co-employment and project-management worries. We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment. • Compensation Range: $75,000 - $85,000 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionCompany Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Job Description Eurofins Lancaster Laboratories, a nationally recognized laboratory, is searching for a GMP Chemist in our Professional Scientific Services group in Foster City, CA. QC Chemist Responsibilities: • Support the qualification and requalification of Reference Standards through analytical testing techniques such as Appearance testing, FTIR, NMR, Liquid Chromatography (LC/HPLC/UPLC), TGA, DSC, and Karl Fischer titration, including performing correction factor calculations., • Ensure adherence to GMP regulations by completing required training, following Standard Operating Procedures (SOPs), and maintaining compliance-related documentation., • Review and verify laboratory documentation, calculations, and test preparations before sample analysis to help prevent deviations and laboratory investigations., • Perform data analysis and troubleshoot methods and instrumentation., • Prepare data for presentations and assist in generating technical reports, • Coordinate sample shipments and testing activities with external contract laboratories, and accurately document and upload analytical results into internal databases., • Work closely with cross-functional teams and external vendors, contract laboratories, and partners to support operational goals., • Initiate and perform investigations, as needed, • Write protocols and technical reports and transfer methods internally and externally, • Contribute to a safe, organized, and compliant laboratory environment by participating in routine housekeeping and weekly laboratory cleanup activities.Qualifications The Ideal Candidate would possess: • Demonstrated success in executing small molecule analytical chemistry methods adhering to SOPs and GMP guidelines., • At least 1 year of continuous experience in GMP/ GLP regulated environment., • Previous experience conducting and analyzing data for analytical methods such as UPLC/HPLC, FTIR, NMR, Thermogravimetric DSC/TGA, and KF titrations., • Understanding of experimentation and data analysis using Empower software (Version III), • Excellent written and verbal communication skills and experience interacting with people from a wide range of skill levels and experience, • Ability to communicate complex scientific findings and recommendations in one-on-one discussions and departmental meetings, • Excellent technical writing experience such as protocols, reports, and SOPs, • Demonstrated ability to work as an independent, self-motivated, detail-oriented, result-driven and highly flexible team-player in a fast-paced working environment, • Strong computer, scientific, and organizational skills, • Demonstrated exceptional attention to detail and strong project management capabilities, effectively managing project resources, including materials, personnel, and timelines, while proactively identifying and escalating critical issues to project leadership and management., • Ability to work independently and as part of a team with internal and external clients, self‑motivation, adaptability, and a positive attitude, • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Qualifications • B.S. in Chemistry or related scientific field and minimum of 2-5 years of experience in an analytical environment, or M.S. degree and 1-3 years of experience, • Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information • Excellent full time benefits including comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match, • Paid vacation and holidays, • Compensation Range: $60,000 - $70,000 Eurofins Lancaster Laboratories Professional Scientific Services® (PSS) is a global, award-winning insourcing solution that places our people at our clients’ site dedicated to running and managing laboratory services while eliminating headcount, co-employment and project-management worries. We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment. Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionSalary: $90K-$95K, DOE Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to support the life sciences industry by cultivating and empowering exceptional scientists to deliver specialized laboratory services that advance research, foster collaboration, and accelerate innovation through quality and a shared commitment to excellence. We can offer you the chance to build on your skills and knowledge while working among experts in their fields and with cutting-edge instrumentation. Cogent Scientific offers competitive pay, attractive benefits (such as medical/dental/vision insurance; 401(k); parental leave; PTO and paid holidays; etc.) and an exciting work environment. This position may include relocation benefits as well. We aim to recruit the best people who stand out among their peers and embody our Core Values: Client Focused: We only succeed when our clients succeed. Outstanding: We deliver meticulous results through outstanding performance. Good: We act ethically and morally. Employee-Centric: We honor and support our employees. Nimble: We are prepared to adapt in an ever-changing industry. Team-Oriented: We collaborate with each other and with our clients. We currently have a role available for a Pharma Bioanalytical Chemistat our South San Francisco site. Job duties include, but are not limited to: • Supporting Bio-Analysis sample preparation, design and perform mass-spec analysis as well as data analysis/interpretation from in-vivo studies from triple-quad mass spectrometers (Sciex 7500), • Characterization of recombinant proteins, antibodies, and ADCs using intact-MS and peptide mapping for routine QC using high-res mass spec platforms (Orbitrap)., • Working closely with a team of scientists to support the development, optimization, and executing analytical assays for protein characterization and bioanalysis to guide large molecule therapeutic design., • Collaborating with the team to meet timelines and deliverables., • Performing general lab maintenance and instrument calibrations. Job requirements include, but are not limited to: • BS - Chemistry, Biochemistry or related field with 2-5 years industry experience or MS with 1-2 years industry experience in a mass spec focused lab on antibodies/ADCs/ proteomics or in a relevant scientific discipline focused on mass spec and ADCs., • Excellent communication skills verbal and written., • Works well both as a team and as an individual., • Demonstration of excellent team player skills, very strong attention to detail, very strong problem-solving skills, a high level of learning agility, and the ability to work across functions. The ideal candidate will be enthusiastic and self-motivated, with the leadership and communication skills necessary to operate effectively in a fast-paced multidisciplinary environment with flexibility and an adaptable approach to goal delivery. This is a day shift position (approx. 8a-5p local time). Cogent Scientific provides equal employment opportunities to all applicants and does not discriminate based on any legally protected characteristic. Additionally, if you require a reasonable accommodation during the application or interview process, please let us know. This job posting will remain open until 8/10/2026 or until a qualified candidate has been selected, whichever comes first.

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

A healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That's what makes us Genentech. The Opportunity We are seeking a highly motivated and experienced Medicinal Chemist (Senior Principal Scientist) to join our innovative research and development team. This is a technical leadership position within our Peptide Therapeutics department, focused on advancing Peptide Therapeutics. The ideal candidate will be a significant contributor and a proven leader, responsible for optimizing and advancing novel peptide therapeutics into clinical development. You will lead the Medicinal Chemistry efforts for a highly integrated and collaborative team, applying your deep scientific expertise to solve complex drug discovery challenges and drive projects forward. Key Responsibilities • Drive the discovery of novel peptide therapeutics. Govern the design and synthesis of innovative peptides and peptidomimetics with enhanced potency, stability, and pharmacokinetic properties., • Lead scientific and project teams from concept to clinic. Initiate and lead new research projects, guiding them from early hit identification through lead optimization, with the ultimate goal of advancing promising compounds to clinical development., • Implement rational drug design strategies. Apply a broad repertoire of skills, including peptide synthesis, conformational analysis, and computational methods to implement strategic structure-activity relationship plans that optimize the pharmaceutical properties of peptide leads., • Champion cross-functional collaboration. Lead or co-lead multidisciplinary teams, serving as a key scientific partner to colleagues in Research Biology and Drug Discovery to overcome complex challenges associated with the development of peptide therapeutics., • Provide scientific leadership and mentorship. Supervise and mentor junior scientists, contribute to the prioritization of team objectives, and propose future strategies to meet broader portfolio goals., • Ensure data integrity and project success. Oversee the analysis and interpretation of complex analytical data, including mass spectrometry, HPLC, and NMR, to confirm compound identity and purity. You will be responsible for managing multiple projects simultaneously, delivering high-quality results on time. Who You Are • Education: Ph.D. or postdoctoral degree in Organic Chemistry, Medicinal Chemistry, or a related field., • Experience: A minimum of 7 years of experience in the biotechnology or pharmaceutical industry, with a proven track record of advancing drug candidates from the conceptual stage into clinical testing. Technical Expertise: • Demonstrated mastery in complex molecule organic synthesis, including proficiency in both automated solid-phase peptide synthesis, and solution-phase small molecule synthesis, utilizing state-of-the-art protecting group and purification strategies., • Must possess expertise in high-throughput and parallel synthesis for library generation, coupled with the expert ability to analyze and interpret all relevant analytical data (HPLC, Mass Spectrometry, NMR) to confirm the identity and purity of all synthesized drug candidates., • Required experience in designing, developing, and implementing novel synthetic routes to overcome challenging chemical and physicochemical issues associated with optimizing both peptide and small molecule scaffolds., • Must possess deep experience in the design and multi-step synthesis of novel, non-commercial building blocks and scaffolds to enable SAR exploration and overcome property liabilities., • Deep knowledge of macrocyclic peptides, including the properties required for different routes of administration (i.e. IV vs SC vs PO, etc), and related library-based screening technologies (e.g., OBOC, mRNA display, AS/MS). Computational Methods: • Experience with computational modeling and simulation for peptide design and optimization, including conformational sampling and molecular dynamics (MD) simulations., • Proficiency in structure-based drug design and ligand-based drug design to guide peptide modifications., • Familiarity with machine learning and AI-driven platforms for predicting peptide properties, optimizing sequences, and generating novel scaffolds., • Experience using common computational chemistry software (e.g., Schrdinger, MOE, Maestro, or similar). Leadership & Collaboration: • Demonstrated success in a leadership role, guiding multidisciplinary teams to deliver drug candidates., • Exceptional communication and presentation skills, with the ability to inspire and lead within a globally matrixed organization., • A highly collaborative and transparent style, with a proven ability to mentor junior scientists and build strong relationships across all levels of the organization. Relocation benefits are available for this posting. The expected salary range for this position based on the primary location of California is $168,600 to $313,000. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

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