Sr Process Development Engineer- Med Device- Mount Laurel, NJ

As a Senior Process Development Engineer, you will design, implement, and validate manufacturing processes for cutting‑edge implantable electronic medical devices. You'll lead engineering initiatives, improve production capabilities, and collaborate cross‑functionally to support next‑generation medical technologies in Mount Laurel, NJ.

Client Details

Our client is a fast‑scaling medical technology innovator developing breakthrough therapeutic solutions that transform the lives of patients with chronic, life‑limiting conditions. They are mission‑driven, globally expanding, and committed to building inclusive teams that advance medical science and improve patient outcomes in Mount Laurel, NJ.

Description

The Senior Process Development Engineer will:

• Develop, validate, and optimize manufacturing processes for implantable electronic medical devices.
• Lead equipment specification, procurement, installation, and validation activities.
• Oversee design and acquisition of manufacturing fixtures, tooling, and semi‑automated systems.
• Guide processes involving welding, soldering, cleaning, molding, and surface treatments.
• Perform DOE studies, root‑cause analysis, and process optimization initiatives.
• Mentor engineers and technicians, sharing technical leadership and best practices.
• Partner with Supply Chain, Quality, and R&D teams to align processes with product requirements.
• Manage supplier/consultant relationships and ensure high‑quality documentation.
• Implement efficient workflows and track engineering KPIs to drive performance excellence.

Profile

The successful Senior Process Development Engineer will have:

• Bachelor's degree in Engineering (Mechanical preferred; advanced degree a plus).
• 5+ years of experience developing manufacturing processes in the medical device industry.
• Experience with implantable pulse generator assembly strongly preferred.
• Proficiency in PFMEA, failure analysis, DOE, and full lifecycle product development.
• Strong knowledge of FDA/ISO medical device regulations and compliance requirements.
• Skilled in statistical tools, CAD/3D modeling, and ideally laser/resistance welding.
• Excellent communicator with strong attention to detail and problem-solving abilities.
• Comfortable working in a fast-paced, collaborative engineering environment.

Job Offer

• Make a direct impact on technologies that dramatically improve patient lives.
• Competitive base compensation plus bonus
• Free healthcare
• Join a high-growth, mission‑focused engineering team shaping next‑gen medical devices.
• Collaborate in an environment that promotes innovation, mentorship, and cross‑functional teamwork.
• Benefit from strong compensation, comprehensive medical coverage, and generous retirement match.
• State of the art facility in Mount Laurel, NJ.

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.