What You Will Achieve
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.
Here Is What You Need (Minimum 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
Bonus Points If You Have (Preferred Requirements)
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, includingrisk management and ethical use
Non-Standard Work Schedule, Travel, or Environment Requirements
This position will cover a Sunday-Thursday shift. Occasional holiday or other off-hours coverage may be required but will be communicated well in advance of time that is required.
Other Job Details:
The annual base salary for this position ranges from $68,600.00 to $114,300.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 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, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.
Relocation assistance may be available based on business needs and/or eligibility.
Candidates must be authorized to be employed in the U.S. by any employer.
U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available onPfizer Careers.
Quality Assurance and Control
