Project Engineer, Biomedical Engineer
Job in
San Rafael, Marin County, California, 94901, USA
Listed on 2026-06-02
Listing for:
Tucker Parker Smith Group (TPS Group)
Contract
position Listed on 2026-06-02
Job specializations:
-
Engineering
Biomedical Engineer, Quality Engineering, Medical Device Industry, Manufacturing Engineer
Job Description & How to Apply Below
Project Engineer Medical Device & Combination Products
Location: 100% Remote
Duration: 5-Month Contract (Potential Extension/ Conversion)
Pay Rate: $96 - 100/hour
Our client is seeking an experienced Project Engineer to support medical device and combination product development activities. This role will focus on design control, risk management, verification testing, and regulatory support for device-related projects within a regulated environment.
Key Responsibilities- Lead and support device and combination product development activities
- Manage design control documentation, DHF, risk assessments, and traceability
- Develop and execute design verification testing and test methods
- Support regulatory submissions and compliance activities
- Coordinate with cross-functional teams, vendors, and CMOs/CDMOs
- Support human factors engineering studies and manufacturing activities
- Author technical documents including protocols, reports, SOPs, and work instructions
- Drive product and process improvements through change control processes
- BS in Engineering or related field required; MS preferred
- 8 10+ years of medical device or combination product development experience
- Strong experience with:
- Design controls
- Risk management (DFMEA, PFMEA, UFMEA)
- Design verification & validation
- DHF documentation
- Regulatory standards (FDA, ISO, cGMP, QSR)
- Experience working with external vendors, CMOs, or CDMOs
- Strong communication and project coordination skills
- Auto injectors, prefilled syringes, needle safety devices, or on-body devices
- Human factors engineering support
- Design for Manufacturability (DFM) and Design for Assembly (DFA)
- Solid Works or similar design software experience
SKILLS:
" 10+ years of experience as a Project Engineer
" 3-5+ years of experience as a Device Engineer on an injectable combination product development product.
" Direct experience developing design controls for autoinjectors and syringe products.
" Ability to discuss examples of design requirements documents, risk management files, trace (traceability matrix), specifications, design outputs, and drawings.
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