Sr. Device 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

Sr. Device Engineer### Sr. Device EngineerApply: United States - New Jersey - Parsippany: Full time: Posted Today: 4956467**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 useOTHER JOB DETAILSLast Date to Apply for Job: June 2nd, 2026.Referral Bonus Eligibility: YESEligible for Relocation Package: NOWork Location Assignment: HybridThe 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.**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 regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.**EEO & Employment Eligibility**Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email [e-mail]. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.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.