- Responsibility for all quality system activities, including internal auditing, quality awareness training, supplier/contract manufacturing organization auditing, document control, CAPA's, Vigilance activities, MRB, and quality improvement meetings.
- Supporting R D initiatives focused on the chemical aspects integral to product development
- Continuous enhancement of Quality Assurance policies, procedures and systems to ensure compliance with the regulatory standards.
- Managing the QA team.
Requirements: - Bachelor's degree (BSc) or higher in life sciences, biology, chemistry, biotechnology, or related fields - required.
- Must possess extensive knowledge of quality requirements.
- Experience and understanding of regulatory requirements in the Medical Device field.
- At least 5 years of management experience in the medical device or pharmaceutical industry.
- Fluent in English.
This position is open to all candidates.
