Use Your Power for Purpose
This role has primary responsibility for confirmation that medical devices and drug/device combination products meet their intended function. This includes development of data through engineering studies that informs new product development as well as test reports that support product submissions. The candidate will work within a team environment to solve problems and utilize best engineering practices and techniques for root cause and statistical analysis. This work entails defining test methods, developing protocols, performing data analysis, and writing reports in compliance with corporate procedures.
What You Will Achieve
In this role, you will:
Partner with Systems engineers in defining product requirements such that they are verifiable
Development of test fixtures, test methods, and performance of Test Method Validation activities
Coordinate with internal and external partners and suppliers to procure test samples and manage conditioning and accelerated aging studies
Ensure integrity and compliance of data according to Standard Operating Procedures
Develop Verification Plans including test strategy
Utilize technical writing and statistical data analysis skills to write protocols and reports
As necessary, conduct root cause analysis and derive recommendations based on analysis of data
Translate inspections and tests methods into component and product specifications
Potential for Project Team lead responsibilities including MS Project schedule creation/maintenance, device team meetings, and overall team management.
Here Is What You Need (Minimum Requirements)
Bonus Points If You Have (Preferred Requirements)
Experience in the pharmaceutical or biotechnology industry
Familiarity with Good Manufacturing Practices (GMP)
Experience with statistical software (e.g., Minitab, JMP)
Ability to lead cross-functional teams
Strong organizational skills
Adaptability and flexibility in a dynamic work environment
Ability to mentor and develop junior team members
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
OTHER JOB DETAILS
Last Date to Apply for Job: June 2nd, 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 Pfizers 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 lifes 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 6 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
