Quality Compliance Manager (Part time)

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 management processes aligned with ISO 14971.
• Maintain documentation control systems and ensure process standardization across global operations.

Training & Quality Culture

• Conduct training sessions on QMS and compliance requirements.
• Promote a strong culture of quality and continuous improvement across the organization.

Preferred Profile

• 6–12+ years of experience in Quality Assurance / QMS.
• Hands-on experience implementing ISO 13485.
• Experience handling external audits and certification processes.
• Background in medical device manufacturing preferred.
• Strong process-oriented and documentation management mindset.

If you are passionate about quality, compliance, and building scalable systems in the medical device industry, we would love to hear from you.