Use Your Power for Purpose

Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients.  Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.

What You Will Achieve

You will be a member of Pfizer’s dedicated and highly effective quality assurance team. You will be responsible for providing Quality Assurance support to GMP clinical manufacturing. You will make sure that product and process documents match the specifications based on established sampling and statistical process control procedures. Your expertise will help in identifying deviations from established standards, in the manufacturing and packaging of products. In the relevant cases you will approve investigations to ensure compliance.

As an associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate explaining issues and create a collaborative team environment.

It is your hard work and commitment that will make Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It

• Contribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.

• Review and approve various Good Manufacturing Practices {also cGMP} records (primarily batch records for Drug substance and Drug Product) and investigations.

• Review/Approve Standard Operating Procedures (SOPs) revisions and Validation Documentation (Periodic Reviews)

• Ensure that all documents for batch release are reviewed for completeness and accuracy.

• Make Quality decision to resolve moderately complex issues with assistance from management/Sr. Staff

• Seek out and assess internal and external compliance with applicable regulations.

• Support the site relative to a constant state of inspection readiness. Participate in audits relative to this role as needed.

• Recognize when an issue is beyond your sphere of influence and escalate immediately.

• Participate in Limited Duration Teams, Continuous Improvement (CI) projects, Corrective Action / Preventative Action Effectiveness, etc. as appropriate.

• Assist and support the manufacturing staff in detecting and solving compliance errors in real time during manufacturing operations.

• Help to define appropriate action plans for improvement and follow-up and communicate action closures.

• May participate in the release of raw materials, as needed.

• Procedural Administration/Active Library Support as needed

Here Is What You Need (Minimum Requirements)

• Applicant must have a High School Diploma (or Equivalent) and 6 years of relevant experience OR an Associate’s degree with 4 years of experience OR a Bachelor’s degree with 0 years of experience.

• Experience in pharmaceutical industry

• Sound knowledge of current Good Manufacturing Practices and the applicable GxP regulations and standards.

• Ability to work in a team environment within own team and interdepartmental teams.

• Excellent communication and interpersonal skills

• Proactive approach and strong critical thinking skills.

• Effective written and oral communication skills

• Experience with Digital Applications /Solutions (Co-Pilot, AI applications, eBR, etc)

Bonus Points If You Have (Preferred Requirements)

• Experience at a manufacturing site

• Experience of writing and managing deviations

• Experience in production batch record review, Enterprise Resource Planning system, investigation of non-conformance, root cause analysis and change control management is preferred

Physical/Mental Requirements

• Mental agility to handle a large quantity and broad scope of different types of quality assurance work.

• Ability to work independently, problem solve and make recommendations for solutions.

• Role is primarily office-sitting. Position requires walking, sitting, standing, and carrying batch records from one location to another as Andover site is a campus setting.

• Able to lead and/or participate in person or Microsoft Teams meetings.

Other job details

• Last day to apply: September 21st, 2026

• Work Location Assignment: On Premise

 

 

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 on Pfizer Careers.

 

 

Quality Assurance and Control