VP Regulatory Affairs & Quality Assurance at ALLESET INC

Flowery Branch, Georgia, United States -

Full Time

Start Date

Immediate

Expiry Date

22 Aug, 26

Salary

0.0

Posted On

24 May, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Global Regulatory Strategy, Quality Management Systems, FDA Compliance, EU MDR, ISO 13485, Commercialization Support, Executive Leadership, M&A Due Diligence, Audit Management, Market Access, Stakeholder Influence, Strategic Problem Solving

Industry

Medical Equipment Manufacturing

Description

Global Resources International (GRI) is seeking an experienced and strategic Vice President of Regulatory Affairs & Quality Assurance (RA/QA) to lead global regulatory strategy, quality systems, and commercialization support across highly regulated markets. This executive leadership role is ideal for a forward-thinking regulatory professional who thrives at the intersection of compliance, innovation, quality, and business growth. At GRI, we partner with organizations worldwide to deliver operational excellence, strategic solutions, and regulatory leadership that accelerate success in complex industries. Responsibilities * Lead global regulatory strategy across FDA, EU MDR, and international markets * Drive product approvals, submissions, audits, and agency interactions * Partner with commercial and product teams to accelerate market access and commercialization * Serve as a senior advisor to clients, regulators, and executive stakeholders * Oversee Quality Management Systems (QMS) and continuous improvement initiatives * Build and mentor a high-performing RA/QA organization * Support strategic growth initiatives, including partnerships and M&A due diligence Qualifications * 15+ years of progressive Regulatory Affairs and/or Quality experience * Deep expertise in FDA, EU MDR, ISO 13485, and global regulatory frameworks * Strong executive presence with the ability to influence C-suite stakeholders and clients * Proven success leading regulatory strategy in medical device, pharmaceutical, or life sciences industries * Experience supporting commercialization and market expansion initiatives * Passion for leadership, quality excellence, and strategic problem solving Why Join GRI? At Global Resources International, we believe regulatory excellence is a competitive advantage. This role offers the opportunity to shape global strategy, strengthen client partnerships, and directly influence organizational growth and innovation. If you are ready to make a significant impact in a dynamic and growth-focused environment, we would love to connect with you.

Responsibilities

Lead global regulatory strategy and oversee Quality Management Systems across FDA, EU MDR, and international markets. Partner with commercial teams to accelerate market access and provide senior advisory to executive stakeholders.