Technical Associate, GMP Manufacturing

Responsibilities

• Set up, execute, and evaluate GMP manufacturing unit operations including seed train, bioreactors, centrifugation, filtration, chromatography, UF/DF, conjugation, and lyophilization
• Perform CIP, SIP, aseptic sampling, parts washing, and documentation
• Manage work order generation and data entry/evaluation
• Collaborate with group engineers, development lines, and shift technicians to communicate status and operational challenges
• Maintain a safe work environment at all times

Requirements

• HS diploma, Associates Degree, or BS/BA in Biotechnology, Microbiology, Cell Biology, Chemical Engineering, Biochemistry, or equivalent
• 0 to 2 years of experience in a laboratory or manufacturing environment (bioprocess or chemical process industry)
• Proficiency in Microsoft Office, specifically MS Word and MS Excel
• Excellent oral and written communication skills
• Ability to work under minimal supervision and as part of a matrix development team
• Physical ability to lift 40 lbs and stand for long periods of time

Preferred Qualifications

• Prior experience in a Biological Pilot Plant or Commercial Manufacturing setting
• Knowledge of fermentation and downstream processing techniques

Benefits

• Competitive hourly salary with eligibility for overtime and shift premiums
• 401(k) plan with Pfizer Matching Contributions and additional retirement savings contributions
• Comprehensive health benefits including medical, prescription drug, dental, and vision coverage
• Paid vacation, holidays, personal days, and medical leave
• Paid caregiver and parental leave

About the Company

Pfizer is a global leader in the pharmaceutical industry, dedicated to developing breakthroughs that change patients' lives. Our manufacturing teams play a critical role in ensuring timely access to essential medicines through agile and high-quality production processes.