Use Your Power for Purpose

Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is designed to be flexible, innovative, and customer-oriented. Whether your role involves development, maintenance, compliance, or analysis through research programs, your contribution is crucial and will have a direct impact on patients.  

What You Will Achieve

In this role, you will:

• Investigate quality issues within manufacturing and quality laboratories

• Examine deviations, out-of-specification results, and atypical investigations

• Identify root causes and suggest effective corrective action plans

• Ensure all reports comply with regulatory requirements and company policies

• Contribute to moderately complex projects, managing your own time to meet targets

• Develop plans for short-term work activities within a collaborative team environment

• Apply skills and discipline knowledge to contribute to work within the Work Team

• Make decisions to resolve moderately complex problems in standard situations

• Work under general supervision, following established procedures and general instructions

• Periodically review work, and may review the work of other colleagues in a mentor role

Here Is What You Need (Minimum Requirements)

• BA/BS with at least 2 years of experience or MBA/MS with any years of experience or associate's degree with at least 6 years of experience or high school diploma (or equivalent) with at least 8 years of relevant experience

• Proven record of problem-solving and decision-making skills

• Experience in the pharmaceutical industry

• Strong background and knowledge in manufacturing, compliance, and technology investigations, processes, and systems

• Ability to work both independently and collaboratively

• Effective communication skills, both written and verbal

• Computer literate with superior skills in managing Excel spreadsheets

Bonus Points If You Have (Preferred Requirements)

• Master's degree

• Experience with investigations, including conducting and writing investigations using methodology

• Familiarity with regulatory requirements and quality standards

• Strong analytical and critical thinking skills

• Ability to manage multiple projects simultaneously

• Experience with root cause analysis and corrective action plans

• Excellent organizational skills

• Ability to mentor and guide junior colleagues

• Strong interpersonal skills and the ability to foster a collaborative team environment

• 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

  
 

PHYSICAL/MENTAL REQUIREMENTS

• Specific area/grade gowning required.

• Capable of residing in a controlled environment for more than three (3) hours.

• Capable of standing for periods of more than one (1) hour.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

Position shift: 8 am to 5 pm (flexible). 

Most be able to support investigation process after hours as needed.

OTHER JOB DETAILS

Last Date to Apply for Job (Internal Candidates): July 28th, 2026

Last Date to Apply for Job (External Candidates): August 4th, 2026


The annual base salary for this position ranges from $82,700.00 to $137,900.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 10.0% 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