Research and Development Project Manager
Listed on 2026-06-05
-
Engineering
-
Management
This role is for one of the Weekday's clients.
Now Hiring:
Senior Project Manager - R&D | Medical Device New Product Development
Location:
San Clemente, CA (Hybrid)
Competitive Salary. Long-Term Role. Various shifts might be available, with compensation varying based on the selected shift.
We are currently looking for a seasoned Senior Project Manager with extensive experience in Medical Device New Product Development (NPD) to lead enterprise-level R&D projects within a highly regulated healthcare setting. The successful candidate should possess practical expertise in managing products throughout the entire medical device development process — including design inputs, verification and validation, regulatory submissions, and product launch.
Requirements- Extensive experience in Medical Device New Product Development (NPD)
- In-depth knowledge of Design Controls
- Proven background in supporting FDA 510(k), MDR, and other regulatory submissions
- Capacity to perform effectively in fast-paced and ambiguous R&D settings
- Demonstrated track record of driving alignment across cross‑functional teams including R&D, Regulatory, Quality, Operations, and Supply Chain
- Experience with supporting product launch and ongoing sustaining engineering efforts
- Lead complex R&D and New Product Development initiatives within FDA-regulated contexts
- Oversee project execution from initial concept through to commercialization
- Manage schedules, budgets, resources, risks, and deliverables associated with projects
- Coordinate multidisciplinary teams such as Regulatory Affairs, Quality, Manufacturing, Operations, Marketing, and Supply Chain
- Support design control activities, including product performance, assembly integrity, safety, labeling, packaging, as well as verification and validation tasks
- Collaborate with stakeholders to establish project scope, validation strategies, and requirements in dynamic development environments
- Ensure compliance of all projects with FDA, ISO 13485, GMP, and MDR standards
- Deliver executive‑level project status updates and communications
- Bachelor's degree mandatory
- Minimum of 4 years' experience in Project Management within Medical Device or regulated healthcare industries
- Experience in Design Controls and Medical Device Development Lifecycle
- Strong comprehension of NPD processes and regulatory frameworks
- Skilled in MS Project, Excel, PowerPoint, SharePoint, and other related project management tools
This role represents a fantastic opportunity for a self‑driven individual who excels in early‑stage product development and can lead execution across multiple teams independently.
#J-18808-Ljbffr(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).