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Research and Development Project Manager

Job in San Clemente, Orange County, California, 92674, USA
Listing for: Weekday AI (YC W21)
Full Time position
Listed on 2026-06-05
Job specializations:
  • Engineering
  • Management
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below

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
Primary Responsibilities
  • 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
Required Qualifications
  • 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.

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