Senior Associate Scientist Mammalian Bioanalytics

• Participate in the development, qualification, validation, and transfer of qPCR, ELISA, MSD, cell-based assays and potentially other analytical methods in a regulated GMP environment.

• Perform routine cell culture activities such as thawing, passaging and banking cells.

• Cross train in separation techniques such as cIEF, CE-SDS and SEC and support GMP release and stability testing as needed

• Perform cGMP sample testing according to standard operating procedures (SOPs) and compile data packets.

• Assist in the drafting of SOPs and technical reports and be able to effectively communicate progress and experimental results to supervisor and team members.

• Support Analytical equipment maintenance by performing regular scheduled activities to comply with GMP standards to maintain a GMP compliant laboratory.

• Ensure timely completion and delivery of all analytical results and documentation (technical reports, SOPs, ELN, LIMS, etc.) to support product development during clinical phases.

• Bachelor’s degree in Biology, Biochemistry, Immunology, Molecular Biology, Cell Biology or related discipline with a minimum of 2 years of relevant experience in the biotechnology/pharmaceutical industry OR Master’s Degree with a minimum of 6 months of experience (academic experience will be considered).

• Hands-on experience with at least one of these methods: ELISA, qPCR, MSD, cell-based assays techniques.

• An understanding of Biology, Biochemistry, Biophysical methods.

• Must be organized, efficient, and able to work according to timelines.

• Excellent organizational and communication skills.

• Must be able to work collaboratively in a fast-paced, team-oriented environment.

• Basic understanding of methodology and hands-on experience with ELISA, qPCR, MSD, cell-based assays techniques in a pharmaceutical or biotechnology setting.

• Intern or co-op experience working in a laboratory environment.

• Working experience in a GMP environment and ability to adhere to all appropriate GMP standards (e.g. invalid result investigations, deviations, and CAPAs).

• Proficient in Microsoft Word, Excel, PowerPoint, and ELN.

• Make your work count by supporting a company that brings life-changing treatments to millions — and is committed to doing right by patients, communities, and the planet.

• Drive progress from within by helping simplify, scale, and modernize how a global biopharma business delivers smarter, faster, and more sustainably.

• Support teams across science, medicine, and operations by building better systems, shaping bold strategies, and enabling innovation at speed.

• Make an impact across borders and functions, collaborating with leaders to turn complex challenges into real-world solutions.

• Advance your career through stretch roles, cross-functional moves, and development opportunities designed to match your ambition.

• Thrive in inclusive, high-performing teams where every role matters and every voice helps shape what’s next.

Sanofi US Services and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

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