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Bachelor of Science degree in Engineering, Biology, Chemistry, Pharmacology, Computer Science or a related field with 6+ years of relevant experience. Excellent organization and planning skills and the
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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
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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
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environments. How You Will Achieve It Apply your chemistry expertise. Understand the requirements of other related disciplines (Regulatory, Quality Organization, Project Management, etc.). Demonstrate skills in
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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
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synthesis, high-throughput chemistry screening, biocatalysis, photocatalysis, and flow chemistries) to drive advancement of programs across the small molecule portfolio. The candidate will work directly with
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synthesis, high-throughput chemistry screening, biocatalysis, photocatalysis, and flow chemistries) to drive advancement of programs across the small molecule portfolio. The candidate will work directly with
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) 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
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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
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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