Research and Development Project Manager at Weekday AI

San Clemente, California, United States -

Full Time

Start Date

Immediate

Expiry Date

30 Aug, 26

Salary

0.0

Posted On

01 Jun, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Medical Device New Product Development, Design Controls, FDA 510(k), MDR, Project Management, Verification and Validation, ISO 13485, GMP, Cross-functional Leadership, MS Project, Excel, PowerPoint, SharePoint, Sustaining Engineering, Regulatory Submissions, Product Launch

Industry

technology;Information and Internet

Description

This role is for one of the Weekday's clients 🚨 Now Hiring: Senior Project Manager – R&D | Medical Device New Product Development 📍 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. 🔹 Qualifications We Seek: ✔ 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. Must-have skills R&D medical device Medical Devices Medical Device R&D Biomedical Device Design Biomedical Devices

Responsibilities

Lead complex R&D and New Product Development initiatives for medical devices from initial concept through commercialization. Coordinate cross-functional teams to ensure compliance with FDA, ISO 13485, and MDR standards while managing budgets and schedules.