Senior Quality Manager – Medical Devices
About the Role
Skills Alliance is proud to partner with leading organisations in the medical device sector. We are currently seeking a Senior Quality Manager with 5+ years of experience to lead and support quality assurance activities, ensuring compliance with global quality standards and regulatory requirements.
Responsibilities
- Lead and manage the implementation and maintenance of the Quality Management System (QMS) in compliance with ISO 13485, FDA 21 CFR Part 820, MDR, and other relevant standards.
- Oversee internal and external quality audits, including supplier and notified body audits.
- Drive continuous improvement initiatives related to quality processes and compliance.
- Manage CAPA, non-conformances, risk management, and change control activities.
- Collaborate closely with R&D, Manufacturing, and Regulatory teams to ensure quality standards are met throughout product lifecycle.
- Provide leadership and training to quality teams and cross-functional departments on quality systems and compliance.
- Monitor and report on key quality metrics to senior management.
Requirements
- Degree in Life Sciences, Engineering, or related field.
- 5+ years of experience in quality assurance within the medical device industry.
- Strong knowledge of ISO 13485, FDA QSR, MDR, and risk management (ISO 14971).
- Proven experience leading quality teams and managing quality systems in regulated environments.
If you’d like to explore exciting opportunities in medical devices, apply now or connect with me directly for a confidential conversation.
Details
- Seniority level: Mid-Senior level
- Employment type: Full-time
- Job function: Quality Assurance
- Industries: Medical Equipment Manufacturing
