Global Head of Quality, Regulatory & Development

Sinclair; Almere; Remote; EUR 180,000 - 260,000; Full time

Job summary

Sinclair is seeking a Chief Development Officer to lead Quality, Regulatory Affairs, Vigilance and Product Development across our injectable aesthetics portfolio. The role sits on the Executive Leadership Team and shapes global quality systems, regulatory strategy and lifecycle management.

The ideal candidate has extensive leadership in injectable aesthetics, MDR compliance and managing audits with cross-functional teams in international markets.

Qualifications

• Bachelor's degree in Life Sciences or related discipline.
• Minimum 15 years in aesthetics/pharma with injectable products.
• Minimum 10 years leadership in QA and Regulatory Affairs.
• Deep knowledge of EU MDR, ISO 13485, Design Control.
• Experience leading audits and regulatory remediations.

Responsibilities

• Provide executive leadership for global QMS.
• Ensure regulatory compliance with EU MDR and ISO13485.
• Lead audit readiness and remediation programs.
• Oversee CAPA, supplier quality, and risk management.
• Develop global regulatory strategies for injectable portfolio.
• Lead regulatory submissions and lifecycle management.

Skills

Leadership

Quality Assurance

Regulatory Affairs

MDR compliance

GxP / QMS

Education

Bachelor's in Life Sciences

Job description

Sinclair is seeking a Chief Development Officer to lead Quality, Regulatory Affairs, Vigilance and Product Development across our injectable aesthetics portfolio. The role sits on the Executive Leadership Team and shapes global quality systems, regulatory strategy and lifecycle management.

The ideal candidate has extensive leadership in injectable aesthetics, MDR compliance and managing audits with cross-functional teams in international markets.