Senior Associate Scientist

Pfizer Pfizer · Pharma · MO

This role focuses on conducting qualitative and quantitative analyses of compounds and biologics, performing analytical method lifecycle activities (development, validation, transfer), and maintaining records in compliance with GLP/GMP. It involves laboratory instrument maintenance, data presentation in project meetings, and troubleshooting analytical assays for early and late-stage products in a cGMP environment. The role requires a BA/BS or Master's degree with relevant experience in biotherapeutics testing within a GMP setting, strong documentation skills, and experience with method validation and analytical chemistry techniques.

What you'd actually do

  1. Conduct qualitative and quantitative analyses of various compounds and biologics to determine their properties during chemical syntheses, fermentation, or drug product development
  2. Perform analytical method lifecycle activities such as development, validation, and transfer activities for both small molecules and complex formulations
  3. Maintain written records of all experimental work in compliance with GLP/GMP and departmental SOPs
  4. Responsible for performing and troubleshooting analytical assays, while applying these methods across a board range of early and late-stage products in a cGMP environment.

Skills

Required

  • BA/BS with 3 to 5 years of experience performing biotherapeutics testing in a GMP environment OR Master's Degree with 4 to 6 years of experience performing biotherapeutics testing in a GMP environment
  • Strong documentation skills
  • Attention to detail
  • Experience with method validation
  • Ability to extract relevant information from scientific literature
  • Proficiency in recording observations, facts, data, and conclusions during experimental work or cGMP investigations
  • Solid understanding of fundamental analytical chemistry, including functional group recognition and compound characterization
  • Experience using spectroscopic and chromatographic techniques
  • Experience in GMP laboratory operations and logistics
  • Effective interaction with peers and leaders as part of a multi-disciplinary team
  • Strong verbal and written communication skills

Nice to have

  • Understanding of various scientific software or software used in pharmaceutical or production environments
  • Good Laboratory Practices (part of GxP) and Good Manufacturing Practices (also cGMP) knowledge
  • Problem-solving skills and the ability to make decisions based on limited options
  • Initiative and proactive approach to tasks and projects
  • Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity.
  • Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use

What the JD emphasized

  • GLP/GMP
  • cGMP environment
  • method validation