Associate Principal Scientist – Biologics Potency
USA - New Jersey - Rahway
Job Description
Position Description:
Associate Principal Scientist – Biologics Potency
We are seeking a highly motivated and experienced Associate Principal Scientist to join our Biologics Potency team within the Cell Based Sciences, Analytical Research and Development organization of our Research & Development Division.
The primary role of the successful candidate will be to lead the design, method development, optimization and transfer of immune- and cell-based assays for drug substance and drug product release, stability, and characterization that reflect the mechanisms of Action (MoAs) for our Biologics pipeline. As part of this role, they will author and review CMC sections of regulatory submissions and associated source technical reports and risk assessment documents. The ideal candidate should bring expertise in a wide variety of immunological and cell methods and technology for assessment of biological potency with an emphasis on subject matter expertise related to potency assays for biologicals and new drug modalities.
The qualified candidate will be responsible for program potency strategy, developing, establishing pre-qualification and robustness, and transferring immunoassays and cell-based potency assays to assess the biological activity of various biologics modalities such as antibodies, multifunctional proteins, peptide therapeutics, antibody-drug-conjugates, and novel biologics. In our framework of scientific excellence, the associate principal scientist will be an active individual contributor and guide fellow scientists to the design, execution, and interpretation of potency assays, as well as to the ongoing innovation by proposing, evaluating, and implementing innovative approaches in the field of potency assays.
The successful candidate would have a deep understanding of underlying biological mechanisms and assay principles, with experience in key techniques, such as immunoassay platforms, stable cell line generation and/or cell-based assay development to assess the potency of drug candidates. Experience with multiple techniques and technologies, e.g. flow cytometry or lab automation, will be advantageous. The successful candidate should cultivate and foster scientific and technological innovation, leverage external networks to stay current on industry best practices and emerging technologies in potency assay development, champion new initiatives, and seek to enhance functional capability and operational excellence.
The candidate will need to communicate results effectively, write technical reports, advise fellow scientists, and participate in cross-functional teams. Experience of working in a GxP regulated laboratory environment for routine sample testing, documentation, and data verification will be a plus. Experience of working with novel biological drug modalities will be a plus.
Position Qualifications:
Education Minimum Requirement:
Ph.D. in immunology, cell biology, bioengineering, biological …
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Hybrid Hybrid work model
Benefits/PerksFlexible work arrangements Hybrid work
Tasks- Data Analysis
Analytical Research Automation Biologics Collaboration Communication Data analysis Design Flow cytometry Innovation Regulatory Submissions Research and development Scientific Excellence Statistics Technical
Experience4 years
EducationBiological Sciences Biology Business Cell Biology Statistics
TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9