Senior Process Development Engineer/Manufacturing Process Engineer – Implantable Medical Devices
Job in
Marlton, Burlington County, New Jersey, 08053, USA
Listed on 2026-06-27
Listing for:
Jacobs Management Group
Full Time
position Listed on 2026-06-27
Job specializations:
-
Engineering
Manufacturing Engineer, Quality Engineering, Process Engineer, Biomedical Engineer
Job Description & How to Apply Below
Join A Mission-Driven Medtech Team
Join a mission-driven Med Tech team developing breakthrough therapy for heart failure patients worldwide. In this role, you will build and optimize the manufacturing processes behind a life-changing implantable technology that restores hope for patients with limited treatment options. If you want your engineering work to directly impact lives, this is the opportunity.
Why You Should Apply- Join a fast-growing medical device company where engineers have real impact
- Work on breakthrough implantable technology improving outcomes for heart failure patients
- 100% employer-paid medical coverage for employee and family
- Annual bonus eligibility + 401(k) match up to 6%
- Paid vacation, holidays, floating holidays, and sick time
- Develop, implement, and validate manufacturing processes for implantable electronic medical devices
- Specify, procure, install, and validate production equipment and tooling
- Support manual and semi-automatic assembly processes
- Drive advanced manufacturing methods including laser welding, resistance welding, soldering, molding, and surface treatment
- Run DOE studies, perform process optimization, and analyze cross-section samples
- Collaborate with Quality, Supply Chain, and R&D on product requirements
- Provide technical leadership and mentorship to engineering teams
- Maintain detailed engineering documentation and track process KPIs
- Be able to do the job as described.
- Experience developing manufacturing processes for implantable medical devices
- Expertise with laser welding, resistance welding, or implantable device assembly
- Strong knowledge of PFMEA, failure analysis, and Design of Experiments
- Familiarity with FDA regulations and ISO standards for medical devices
- Experience using CAD or 3D modeling tools
Position Requirements
10+ Years
work experience
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