What You Will Achieve
In this role, you will:
Investigate and write or review Laboratory Investigations and/or Non-Conformance Deviations.
Support the Quality Control Organization by supporting trending, department-wide initiatives, investigation training, and continuous improvement activities.
Maintain compliance with Current Good Manufacturing Practices in Quality Control laboratories.
Utilize Laboratory Information Management System and other data systems as warranted.
Serve on cross-functional teams, participate in audits, conduct safety inspections, recommend corrective actions, and train junior colleagues.
Here Is What You Need (Minimum Requirements)
Applicant must have a bachelor's degree with at least 2 years of experience; OR a master's degree with 0+ years of experience;
OR an associate's degree with 6 years of experience; OR a high school diploma (or equivalent) and 8 years of relevant experience
Strong problem-solving abilities
Understanding of pharmaceutical manufacturing, Quality Control testing, packaging, and quality assurance operations
Detail-oriented with robust knowledge of quality systems
Ability to receive feedback and takes accountability for actions and personal development
Strong project management skills
Effective written and verbal communication, as well as interpersonal skills
Bonus Points If You Have (Preferred Requirements)
Relevant pharmaceutical experience
Strong understanding of computer system hardware, infrastructure, and networks
Experience with Laboratory Information Management Systems (LIMS)
Proficiency in data analysis and interpretation
Knowledge of regulatory requirements and guidelines
Laboratory experience
Effective time management and organizational skills
Ability to mentor and train junior colleagues
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
PHYSICAL/MENTAL REQUIREMENTS
Normal lifting, sitting, standing and walking requirements to facilitate support of staff in the office and on the floor (laboratory, suites, etc.).
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Position is first shift Monday through Friday. Some off hour (night/weekend/holiday) support may be required to support staff and operations.
OTHER JOB DETAILS
Last Date to Apply for Job: June 26, 2026.
Referral Bonus Eligibility: YES
Eligible for Relocation Package: NO
Work Location Assignment:Hybrid
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 Pfizer27s 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 life27s 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 2D 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.
Quality Assurance and Control
