Senior Medical Device Verification Engineer

Pfizer Inc; New Jersey; Hybrid; USD 83,000 - 138,000; Full time

Job summary

Pfizer Inc seeks a Sr. Device Engineer in Parsippany, NJ to confirm medical devices and drug/device combos meet intended function. You will develop data through engineering studies and write compliant reports to support product submissions.

The role involves test method development, protocol writing, root cause analysis, and potential project-team leadership with MS Project - all within a GMP-focused environment.

Qualifications

• Bachelor's or higher in engineering with 2+ years experience, or Master's with 0+ years, or Associate with 6+ years, or high school with 8+ years relevant experience.
• Familiarity with GMP preferred.
• Experience with statistical software and data analysis for device verification.
• Ability to lead cross-functional teams and mentor junior members.

Responsibilities

• Develop verification plans and test strategies for medical devices and drug/device combos.
• Create and validate test fixtures and protocols; perform data analysis and write reports.
• Coordinate with internal/external partners to procure samples and manage aging studies.
• Lead project activities, including schedule management and team meetings when assigned.

Skills

Root cause analysis

Cross-functional leadership

Data analysis

Documentation

Education

Bachelor's degree in Engineering

Tools

Minitab

JMP

Job description

Pfizer Inc seeks a Sr. Device Engineer in Parsippany, NJ to confirm medical devices and drug/device combos meet intended function. You will develop data through engineering studies and write compliant reports to support product submissions.

The role involves test method development, protocol writing, root cause analysis, and potential project-team leadership with MS Project - all within a GMP-focused environment.