Opportunity Description
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...
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