-
Will Achieve You will help Pfizer develop and implement chemistry, manufacturing and controls (CMC) regulatory strategies for small and/or large molecules to meet global regulatory requirements
-
or MS in Chemistry, Biochemistry, or related discipline with at least at least 6 (BS) or 4 (MS) years of relevant GLP work experience is required. Experience and proficiency in separation-based analytical
-
Will Achieve You will help Pfizer develop and implement chemistry, manufacturing and control (CMC) regulatory strategies for large molecules and antibody-drug conjugates to meet global regulatory
-
) Familiarity with version control and collaborative programming (e.g., Git) Strong scientific background, with good working knowledge of biology, chemistry, pharmacology, or toxicology. NON-STANDARD WORK
-
groups (Disease Biology, Chemistry, Computational Biology, Structural Biology, Primary Pharmacology), be adept at building partnerships, and be very team-oriented. Highly motivated, highly organized and
-
. What You Will Achieve You will help Pfizer develop and implement chemistry, manufacturing and control (CMC) regulatory strategies for small and large molecule pharmaceuticals and devices to meet global
-
work in a GMP environment. Comprehensive knowledge of analytical techniques in Chemistry, Bioanalytical, or Microbiology. Relevant pharmaceutical experience. Nice-to-Have Master ' s degree in
-
Will Achieve You will help Pfizer develop and implement chemistry, manufacturing and control (CMC) regulatory strategies for large molecules and antibody-drug conjugates to meet global regulatory
-
impact Qualifications Must-Have Ph.D. level education in ADME sciences, pharmacokinetics, medicinal chemistry and/or related fields (or B.S./M.S. with 7 - 10 years of prior experience) with a strong record
-
the Primary Pharmacology Group (PPG), hit follow-up, lead optimization, External Research Solutions, Medicinal chemistry stakeholders, and Digital and data support to ensure timely, high-quality access