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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.
Job Responsibility:
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
Requirements:
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
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.
Nice to have:
Auto injectors, prefilled syringes, needle safety devices, or on-body devices
Human factors engineering support
Design for Manufacturability (DFM) and Design for Assembly (DFA)