PROCESSING APPLICATION
Hold tight! We’re comparing your resume to the job requirements…

ARE YOU SURE YOU WANT TO APPLY TO THIS JOB?
Based on your Resume, it doesn't look like you meet the requirements from the employer. You can still apply if you think you’re a fit.
Job Requirements of Senior Manufacturing Engineer - Medical Device - Derry, NH:
-
Employment Type:
Full-Time
-
Education:
4 Year Degree
-
Location:
Derry, NH (Onsite)
Do you meet the requirements for this job?

Senior Manufacturing Engineer - Medical Device - Derry, NH
My client is seeking a highly experienced Senior Manufacturing Engineer to drive advanced manufacturing initiatives across their surgical device product lines. In this role, you will lead complex projects, mentor junior engineers, and play a key part in scaling operations while ensuring regulatory compliance and operational excellence.
Client Details
My client is dedicated to improving surgical outcomes through innovation, precision, and quality. As a leader in the development, manufacture, and sale of cutting-edge surgical devices, they pride themselves on creating products that make a real difference in patient care.
Description
The Senior Manufacturing Engineer will report directly into the Engineering Manager and be responsible for:
- Lead the development, validation, and optimization of complex manufacturing processes for high-precision surgical devices.
- Manage cross-functional projects involving new product introductions (NPI), process transfer, and design for manufacturability (DFM).
- Drive continuous improvement initiatives using Lean, Six Sigma, and risk-based approaches to enhance yield, reduce cost, and improve throughput.
- Lead root cause analysis and corrective action implementation for manufacturing issues.
- Author and review detailed process documentation including PFMEAs, validation protocols (IQ/OQ/PQ), work instructions, and technical reports.
- Act as a technical subject matter expert during internal audits, external inspections (e.g., FDA), and risk management activities.
- Collaborate closely with R&D, Quality, and Operations to ensure seamless design-to-manufacture transitions.
- Mentor and guide manufacturing engineering team members, fostering a culture of technical excellence and collaboration.
Apply today for immediate consideration!
Profile
- Bachelors Degree in Biomedical Engineering or a related field
- 10+ years of experience in medical device manufacturing
- Knowledge of regulatory requirements (ISO 13485)
- Proficiency in CAD software (e.g., SolidWorks, AutoCAD)
- Hands-on experience with process validation, fixture design, and lean manufacturing
- Sound analytical and problem-solving skills
- Experience with FEA analysis tools is a plus
- Strong communication skills and ability to work in cross-collaborative teams
Job Offer
- Competitive compensation
- Comprehensive benefits plan
- Career growth opportunities
- Access to high level management
- 401K match
- Excellent work life balance
MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.