Responsibilities

• Lead and implement quality assurance and regulatory strategies for the medical device department across the region.
• Ensure compliance with local and international regulatory requirements.
• Develop and maintain quality management systems to support business objectives.
• Collaborate with cross‑functional teams to ensure product compliance and safety.
• Conduct internal audits and coordinate external audits from regulatory bodies.
• Provide regulatory guidance during product development and market launches.
• Monitor and report on regulatory changes impacting the retail industry and life sciences sector.
• Lead training initiatives to enhance compliance awareness and quality standards within the organization.

Qualifications

• A degree in life sciences, pharmacy, engineering, or a related field.
• Strong knowledge of quality assurance and regulatory requi...