Senior Mgr - Reg Affairs/Quality Assurance
Listed on 2026-01-14
-
Healthcare
Healthcare Management
Senior Mgr - Reg Affairs / Quality Assurance Venture Med Group , Ltd. provided pay range
This range is provided by Venture Med Group , Ltd.. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range$/yr - $/yr
Additional compensation typesAnnual Bonus
Venture Med is a fast‑growing Med Tech innovator advancing vascular and endovascular care. Founded by vascular surgeon Dr. John Pigott, the company developed the FLEX Vessel Prep™ System
, a minimally invasive, non‑balloon endovascular tool designed to optimize vessel preparation and improve outcomes in AV fistula, graft, and peripheral interventions. Backed by a seasoned leadership team with multiple Med Tech scale‑and‑exit successes, Venture Med is entering a major commercial growth phase—expanding nationally and building its clinical and reimbursement infrastructure.
- Join an experienced leadership team with deep vascular and endovascular expertise and a proven track record of building and exiting successful Med Tech companies.
- Help advance a first‑in‑class technology with strong clinical evidence, FDA clearance, and active reimbursement momentum through a current TPT designation.
- Play a foundational role in supporting Venture Med’s commercial organization—building process, culture, and impact in a company on the rise.
The Manager of Regulatory Affairs/Quality Assurance position will be responsible for developing and implementing strategies for worldwide governmental approval to introduce new products to market, provide advice on regulatory requirements, and prepare regulatory submissions and negotiate their approval.
Drive regulatory support across all functional areas to deliver superior products, while maintaining ISO 13485 and MDR certification as well as compliance with FDA regulations and any other market‑driven regulatory requirements.
Drive regulatory/quality strategies, and continuous improvement efforts. Influence product development, regulatory approvals, and quality assurance practices, ensuring our products exceed industry standards and improving patient outcomes worldwide.
This role is hybrid in Plymouth, MN. No sponsorship or relocation will be provided.
Key Responsibilities Strategic Leadership- Develop forward‑thinking regulatory/quality strategies that align with corporate objectives and global regulatory landscapes.
- Lead cross‑functional teams to foster a culture of quality, compliance, and continuous improvement across the business.
- Serve as the regulatory expert for global market entry, product labeling, and manufacturing and sales support activities.
- Develop and implement regulatory strategies/plans, domestic and international, to ensure smooth product introduction and continuous support for currently marketed products for Venture Med and its distributors and partners.
- Prepare FDA submissions for new products and product changes as required to ensure timely approval for clinical studies and market release. Review significant regulatory issues with Senior Management, as necessary, and negotiate submission issues with agency personnel. Maintain the regulatory files for the company.
- Provide on‑going support to product development teams regarding regulatory issues, including submissions, and process control per the Quality System.
- Manage international registration ensuring up‑to‑date registrations. Review international growth strategy and proactively seek registration in select countries.
- Provide support for currently marketed products, including reviewing labeling, promotional material, product changes, web site content, and technical publications.
- Maintain relationships with government agencies and respond proactively to the development and changes of laws, regulations, and certifications. Develop general strategies on how to interact more effectively with agencies and their respective personnel.
- Navigate complex regulatory environments, providing expert guidance during audits, inspections, and regulatory interactions.
- Monitor changes in regulatory requirements and assess the impact on company products and…
(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).