What are the responsibilities and job description for the Project Manager position at SSi People?
Job Title: Project Manager
Location: Cambridge, Massachusetts (On-site)
Job Summary: We are seeking a driven professional to lead complex medical device development and regulatory submission activities within a high-impact portfolio. Our team empowers critical advancements in long-term implantable device innovation and ensures alignment with the highest industry standards.
Responsibilities
By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from SSi People and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here: SSi People Privacy Policy
Location: Cambridge, Massachusetts (On-site)
Job Summary: We are seeking a driven professional to lead complex medical device development and regulatory submission activities within a high-impact portfolio. Our team empowers critical advancements in long-term implantable device innovation and ensures alignment with the highest industry standards.
Responsibilities
- Lead integrated project plans to finalize design control deliverables and complete regulatory Premarket Approval (PMA) Modules, ensuring alignment with key submission milestones and timelines.
- Coordinate with Regulatory Affairs and Quality teams to meet all FDA PMA, Design Controls (21 CFR 820), and risk management (ISO 14971) requirements, as well as support EU MDR transition and technical documentation alignment.
- Oversee device design verification and validation (DV) activities, ensuring protocol completeness, traceability, and readiness for regulatory review, including human factors, bench, and clinical testing coordination.
- Manage clinical product manufacturing supply chain activities, facilitate collaboration with Contract Manufacturing Organizations (CMOs), and support readiness for regulatory review, inspections, and risk mitigation.
- Bachelor’s degree in Biomedical, Mechanical, Electrical Engineering, or a related technical discipline.
- 7–12 years of experience managing complex medical device programs, preferably Class III implantable devices.
- Strong working knowledge of FDA PMA submissions, Design Controls, and regulated manufacturing environments.
- Demonstrated experience coordinating cross-functional and external teams in late-stage, submission-focused programs.
By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from SSi People and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here: SSi People Privacy Policy