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Sanofi Group (Sr.) Scientist, Bioanalysis & Immunogenicity in Cambridge, Massachusetts
About The Opportunity:
Scientist/Sr. Scientist Bioanalysis & Immunogenicity, DMPK
The Bioanalysis and Immunogenicity team within the DMPK department at Sanofi is searching for a (Sr) Scientist to join a team developing and running custom ligand-binding assays for research and development purposes. Assay applications will include pharmacokinetic (PK), immunogenicity (ADA) and biomarker (BM) assays in a non-regulated setting as well as oversight of transfer to and execution of assays at regulated labs for studies.
The applicant is expected to perform and/or oversee bioanalytical and immunogenicity work packages such as method development, qualification, validation and sample analysis. Expertise developing custom immunoassays on platforms such as ELISA, ECL (MSD) and other state-of-the art systems is required. The successful candidate will possess excellent self-organization and documentation skills and will be expected to present and discuss their own scientific results and provide input to project teams. Significant onsite presence will be required to perform and oversee laboratory activities.
We are looking for individuals who have relevant immunoassay development and qualification experience, preferably within the above-mentioned technology fields. Prior hands-on experience in a regulated bioanalytical laboratory (GLP/GCP/GCLP) is a plus.
In This Role You Will:
Scientific responsibility for PK and immunogenicity bioanalysis in both non-regulated and regulated settings
Devise bioanalytical strategy within a project
Design, develop and validate PK, BM and/or ADA assays
PK, BM and immunogenicity analysis to support in vivo and clinical studies
Transfer assays and monitor bioanalytical studies internally to other global R&D sites or externally to CRO partners
Work effectively with global project team members to support non-clinical drug development projects
Report and discuss bioanalytical and biomarker results with integrative knowledge of how the data contributes to the drug development process
Author comprehensive bioanalytical plans and reports as well as relevant sections of clinical study reports, submission dossiers and publications
Actively contribute to scientific discussions and drive technical project progress
About You:
PhD in a life sciences field that includes immunoassay development (e.g. biochemistry, immunology, biology, etc.); or MSc, with 3+ years or BS with 6+ years of relevant experience. Level commensurate with experience.
Strong background in immunoassay development using technologies such as ELISA, MSD, Gyros, etc.
Strong knowledge of immunogenicity and principles of bioanalysis: familiarity with current bioanalytical and immunogenicity regulatory guidance (FDA/EMA/ICH) is a plus
Quality-oriented - Prior experience in a regulated bioanalytical laboratory (GLP/GCP/GCLP) is a plus.
Excellent time management and organization skills
Strong communication (verbal, written, interpersonal, listening) skills
Ability to work independently with minimal supervision
Ability to adapt to rapidly changing priorities
Ability to multi-task and meet timelines in a fast-paced environment
Ability and willingness to work in a laboratory
Team player
Excellent English skills (oral and written)
Knowledge of MS Office (Word and Excel)
Available for full time position with significant on-site presence.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse 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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