Associate Scientist, QC

Pfizer • Andover, MA

13h • $60,200 - $100,400 • Onsite

About The Position

The qualified candidate will join the Analytical R&D organization in Andover, MA, to enable development of biological therapeutics. Within Analytical R&D the candidate will join the Quality Control – Andover Group focused on monoclonal antibodies/fusion proteins/synthetic peptides and other biological modalities. This group supports GMP analytical testing to progress biotherapeutic products in the pipeline; this includes release and stability testing, real time in-process testing support, and technical writing of reports and methods/procedure.

Requirements

• BA/BS with any years of experience
• Experience in Quality Systems within a Good Manufacturing Practices (cGMP) environment
• Proficiency with laboratory data systems
• Hands-on experience or working knowledge in the pharmaceutical industry, particularly in handling analytical instruments
• Understanding of the drug development process for the progression of biological incumbents
• Excellent documentation skills with a high attention to detail
• Strong organizational abilities and a team-oriented mindset
• Must be able to wear PPE (lab coat/gloves/safety shoes/glasses/etc.)
• Position requires occasional light lifting and periods of standing, sitting or walking.
• Permanent work authorization in the United States.

Nice To Haves

• Hands-on analytical experience with biological therapeutics
• Proficiency in operating analytical and physical techniques for the characterization of pharmaceutical substances and products
• Effective interpersonal and communication skills
• Ability to work collaboratively in a team environment
• Strong problem-solving skills
• Experience with advanced analytical techniques
• Knowledge of regulatory requirements and guidelines
• Ability to manage multiple tasks and projects simultaneously
• 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

Responsibilities

• Conduct qualitative and quantitative analyses of organic, inorganic compounds, or biologics.
• Verify the identity, purity, and homogeneity of compounds during chemical syntheses, fermentation, or drug product development processes.
• Prepare and review technical documents, including analytical test methods, standard operating procedures, and investigation reports.
• Independently analyze experimental data and provide conclusions.
• Follow procedures for assigned tasks; seek guidance when needed.
• Conduct experiments for analytical method development, qualification, validation, and characterization of biological therapeutics.
• Present problems and propose solutions in group discussions.
• Complete all required Good Laboratory Practice and safety training, adhering to departmental requirements.
• Maintain appropriate safety practices in the workplace.

Benefits

• 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
• paid vacation, holiday and personal days
• paid caregiver/parental and medical leave
• health benefits to include medical, prescription drug, dental and vision coverage
• Relocation assistance may be available based on business needs and/or eligibility.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Associate degree