QC Scientist I
About The Position
Our breakthroughs would not make it to the hands of patients without our dedicated and agile pharmaceutical manufacturing team. We rely on members who understand the importance and impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and always strive to improve outcomes. You will help ensure that patients and physicians have the medicines they need when they need them. In this role, you will: Perform tasks associated with maintaining Good Manufacturing Practices (cGMP) compliant Quality Control and Stability laboratories. Follow Environment Health and Safety requirements for site and QC laboratories. Perform bioburden and endotoxin testing of routine in-process and drug substance product samples. Support product dispositions through sample review and reconciliation. Support lab activities with routine inventory checks and adhoc requests. Operate within established HR policies and basic colleague relations guidelines. Write Standard Operating Procedures (SOPs), technical reports, project plans, etc.
Requirements
- BA/BS with any years of experience
- Demonstrated experience in manufacturing quality or engineering experience in the biotech or pharmaceutical industry or educational equivalent.
- Fundamental understanding of laboratory instrumentation function and analytical method troubleshooting
- Excellent oral, written, and interpersonal communication skills
- Knowledge of Microsoft Office applications, specifically Word and Excel
- Ability to perform complex mathematical problems and data analysis
- Permanent work authorization in the United States.
Nice To Haves
- A deep understanding of Microbiology testing and experience in defending laboratory practices during regulatory audits
- Solid grasp of aseptic techniques
- Strong problem-solving skills
- Ability to work independently and as part of a team
- Ability to manage multiple tasks 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
- Perform tasks associated with maintaining Good Manufacturing Practices (cGMP) compliant Quality Control and Stability laboratories.
- Follow Environment Health and Safety requirements for site and QC laboratories.
- Perform bioburden and endotoxin testing of routine in-process and drug substance product samples.
- Support product dispositions through sample review and reconciliation.
- Support lab activities with routine inventory checks and adhoc requests.
- Operate within established HR policies and basic colleague relations guidelines.
- Write Standard Operating Procedures (SOPs), technical reports, project plans, etc.
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.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree
