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Project Manager - Class III Medical Implants
Remote / Online - Candidates ideally in
Effingham, Effingham County, Illinois, 62401, USA
Listed on 2026-05-10
Effingham, Effingham County, Illinois, 62401, USA
Listing for:
ProPharma
Remote/Work from Home
position Listed on 2026-05-10
Job specializations:
-
Engineering
Biomedical Engineer
Job Description & How to Apply Below
Responsibilities
- Lead end‑to‑end project management from concept through design, verification/validation, clinical evaluation, regulatory submission activities including PMA preparation, IDE clinical studies, and global regulatory pathways (FDA, EU MDR) where applicable.
- Develop and maintain integrated project plans, schedules, budgets, and risk registers.
- Facilitate cross‑functional project team meetings (R&D, Quality, Regulatory, Manufacturing, Clinical, Marketing).
- Manage project KPIs, timelines, and resource allocations; escalate risks proactively.
- Drive implementation of design controls compliant with 21 CFR 820, ISO 13485, and ISO 14971 risk management requirements: user needs, design inputs/outputs, verification, validation, design transfer.
- Collaborate with engineering teams to ensure design requirements are met for implantable use (biocompatibility, sterilization, packaging, durability).
- Support planning and execution of clinical studies or physician evaluations when required.
- Partner with operations/manufacturing teams to develop scalable, validated production processes.
- Ensure suppliers meet quality and regulatory standards for implantable components.
- Support process validation (IQ/OQ/PQ) and device master record (DMR) creation.
- Communicate project status, milestones, risks, and decision needs to executives and key stakeholders.
- Serve as the primary point of contact for project‑related inquiries.
- Bachelor’s degree required (Engineering, Life Sciences, or related field preferred).
- 5+ years of project management experience in medical devices;
Class III or implantable medical device development experience strongly preferred, including PMA or IDE programs. - Demonstrated familiarity with regulatory frameworks for high‑risk medical devices.
- Experience in cross‑functional leadership and complex product development.
- Deep understanding of design controls, risk management, and medical device quality systems.
- Excellent organizational and planning skills.
- Strong interpersonal and communication skills.
- Ability to manage ambiguity and drive decision‑making.
- Expertise using project management tools (MS Project, Smartsheet, or similar).
Remote working with 20% onsite in Effingham, IL
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