Sr. Device Engineer
PfizerAbout the role
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)
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
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, including risk 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
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.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or r
Apply for this role
Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.
Apply Now →Generate Application KitFree account required — sign up in 30s