Healthcare Product Project Manager - Strategy & Compliance

Regenity Biosciences; Oakland (NJ); On-site; USD 90,000 - 110,000; Full time

Benefits offered by this job

Company performance bonus eligibility

401(k) plan with company contribution

Paid time off and paid holidays

Medical, prescription, dental, and vis

Companypaid life and Accidental Death&

Job summary

Regenity Biosciences in New Jersey is seeking a Project Manager, Healthcare Products to lead cross‑functional programs from concept to commercialization, ensuring timely, on‑budget delivery and rigorous design controls.

You will optimize resource allocation, communicate with stakeholders and executives, and drive PMO continuous improvement while maintaining ISO and FDA compliance in a fast‑paced environment.

Qualifications

• Bachelor's degree required; MBA or Master’s preferred.
• 5+ years in the medical device industry.
• PMI PMP certification preferred.

Responsibilities

• Provide crossfunctional program leadership to drive strategic growth initiatives and programs.
• Execute program plans (schedule, risk management, communication, resources) and communicate status to stakeholders.
• Optimize resource allocation with functional leaders across divisions/site.
• Ensure projects comply with company, FDA, and ISO procedures and guidelines.
• Oversee all phases of product development from concept to commercialization.
• Build and manage stakeholder relationships and communicate with executives.

Skills

Cross-functional leadership

Communication

Stakeholder management

Team collaboration

Education

Bachelor's Degree

Master's Degree / MBA

PMI PMP certification

Tools

MS Project

Smartsheet

Job description

Regenity Biosciences in New Jersey is seeking a Project Manager, Healthcare Products to lead cross‑functional programs from concept to commercialization, ensuring timely, on‑budget delivery and rigorous design controls.

You will optimize resource allocation, communicate with stakeholders and executives, and drive PMO continuous improvement while maintaining ISO and FDA compliance in a fast‑paced environment.