Chief Development Officer
HybridIn English
About the job
Sinclair is looking for a Chief Development Officer to lead global quality and regulatory strategies. This role is based in Almere with a hybrid work mode.
What you will do
- Lead global Quality Management System
- Ensure compliance with ISO 13485, EU MDR, MDSAP and global regulations
- Lead audit readiness and remediation programmes
- Oversee CAPA, supplier quality, complaint management, risk management and quality governance
- Develop and execute global regulatory strategies for injectable products
- Lead regulatory submissions, product registrations and lifecycle management
What you bring
- Bachelor's degree in Life Sciences, Biomedical Sciences, Pharmacy, Chemistry, Engineering or related field
- Minimum 15 years in aesthetics, injectable, pharmaceutical or biologics industry
- Minimum 10 years leadership in Quality Assurance and Regulatory Affairs
- Significant experience with injectable aesthetics products like dermal fillers or collagen stimulators
- Deep knowledge of EU MDR, ISO 13485, Design Control, Clinical Evaluation and Post-Market Surveillance
- Proven experience leading external audits, Notified Body inspections and regulatory remediation
Nice to have
- Previous leadership experience in aesthetics industry or similar injectable aesthetics organisations
- Experience supporting MDR transition programmes
- Experience leading quality and regulatory transformation in a mid-sized international business
- Experience working directly with Boards, Investors or Shareholders
Summary by Personeel.com. The full job description and the application form are on Sinclair's website (sinclair.teamtailor.com); Apply takes you straight there.
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