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Project Manager – Class Iii Medical Implants

Propharma
Propharma
5+ years
Not Disclosed
United States
1 May 7, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L.

Project Manager – Class III Medical Implants | Remote Medical Device Project Management Job in the United States

Company: ProPharma
Job Title: Project Manager – Class III Medical Implants
Location: United States (Remote with 20% Onsite in Effingham, Illinois)
Job Type: Full-Time
Job ID: JR 9642


About ProPharma

ProPharma is a leading global life sciences consulting organization supporting pharmaceutical, biotechnology, and medical device companies across regulatory affairs, clinical research, pharmacovigilance, quality compliance, and medical information services. With more than 20 years of industry expertise, ProPharma helps organizations accelerate product development while maintaining compliance, innovation, and patient safety.


Job Overview

ProPharma is seeking an experienced Project Manager – Class III Medical Implants to lead highly regulated implantable medical device programs from concept development through commercialization.

This role is responsible for managing cross-functional project teams, regulatory activities, design control implementation, manufacturing coordination, and commercialization planning for Class III implantable medical devices. The ideal candidate will have strong expertise in PMA programs, FDA and EU MDR regulations, design controls, and risk management processes within the medical device industry.

This opportunity is ideal for professionals with advanced medical device project management experience who thrive in fast-paced, highly regulated environments.


Experience Required

Experience Level

  • Mid-Senior to Senior-Level Position
  • Not suitable for freshers

Required Experience

  • Minimum 5+ years of project management experience in:
    • Medical Device Industry
    • Implantable Medical Devices
    • Class III Device Development

Preferred Experience

  • PMA (Premarket Approval) programs
  • IDE clinical studies
  • FDA and EU MDR regulatory pathways
  • Cross-functional medical device leadership

Educational Qualification

Required Qualification

  • Bachelor’s Degree in:
    • Engineering
    • Life Sciences
    • Biomedical Engineering
    • Related Scientific Discipline

Preferred Qualification

  • Master’s Degree
  • PMP Certification