About the Role
Taevas Life Sciences is looking for a highly driven Quality & Compliance Lead (Contractual) to establish, maintain, and enhance our Quality Management System (QMS) in line with ISO 13485 and global regulatory standards. This role will play a critical part in ensuring organizational compliance, audit readiness, and process excellence across operations.
Key Responsibilities
ISO 13485 QMS Implementation
Lead end-to-end implementation and maintenance of ISO 13485 QMS. Develop and maintain SOPs, quality manuals, and controlled documentation. Ensure alignment of quality processes across Regulatory, Supply Chain, and Service Delivery functions.Audit & Compliance Management
Plan and conduct internal audits. Prepare teams and documentation for external audits and certification activities. Drive CAPA management and closure of non-conformities.Quality Systems & Process Excellence
Establish and manage CAPA, change control, deviation handling, and risk...Ready to Apply?
Submit your application today and take the next step in your career journey with Taevas Life Sciences.
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