Manufacturing Engineer - Medical Equipment - Peterborough, NH - Peterborough

apartmentMichael Page placePeterborough calendar_month9/9/24

About Our Client

My client is a global leader and dedicated to designing and manufacturing innovative medical devices that improve patient outcomes and advance healthcare worldwide. My client is a CMO with a proven track record of helping teams bring complex components and devices from idea to market.

Job Description

The Manufacturing Engineer will report directly into the Engineering Manager and be responsible for:

Develop, implement, and optimize manufacturing processes to increase efficiency, reduce waste, and improve product quality.
Design, procure, and maintain production equipment and tooling to support manufacturing operations.
Lead and support lean manufacturing initiatives, including Six Sigma projects, to drive process improvements and cost reductions.
Collaborate with the Quality team to ensure compliance with ISO 13485, FDA regulations, and other relevant medical device standards.
Provide technical support to production teams by diagnosing and resolving process issues, ensuring minimal downtime.
Develop and maintain technical documentation, including process flow diagrams, work instructions, and engineering change requests.
Train production staff on new processes, equipment, and quality standards to ensure consistent product quality and efficient operations.

Apply today for immediate consideration!

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.

The Successful Applicant

Bachelors Degree in Biomedical Engineering or a related field
3-5 years of experience in medical device manufacturing
Knowledge of regulatory requirements (GMP's, FDA's 21 CFR 820 and ISO 13485)
Proficiency in CAD software (e.g., SolidWorks, AutoCAD)
Certification in Lean Six Sigma (Green Belt or higher) is preferred.
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

What's on Offer

Competitive compensation
Comprehensive benefits plan
Career growth opportunities
Access to high level management
401K match
Excellent work life balance

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