Key Responsibilities
- Ensuring a consistently high-quality experience for end-users.
- Leading a team to oversee quality activities in assigned markets.
- Monitoring and ensuring quality and regulatory compliance of external manufacturers and distributors, including the identification and resolution of non-compliance.
- Oversee new product introduction and supplier qualification, ensuring continued quality compliance of partners.
- Maintain QMS alignment with international standards, health authorities, regulatory guidelines, and company standards.
- Perform batch release in respective markets to ensure compliance with GMP and regulatory requirements.
- Ensure change controls, deviations, CAPA management, recall activities are managed timely and effectively.
- Oversee new product introduction and supplier qualification process.
Requirements
- Bachelors in Science (or a related discipline).
- At least 10 years' experience in the life science industry (e.g. pharmaceuticals, medical devices, and health supplements) in the quality function with strong technical knowledge in GxP.
- Experience leading teams and quality improvement projects.
- Strong business acumen, problem-solving capabilities, communication skills and stakeholder management are important for this position.
To apply, submit your most updated resume showcasing relevant qualifications and experience.
Not the right opportunity?
We're always looking out for the best talents in the life science industry. If you are currently seeking exciting opportunities within the pharmaceuticals, medical devices, in-vitro diagnostics (IVD), or consumer health industry, do reach out for a confidential chat.
Principal Consultant: Cheong Yee Yin | Registration Number: R22108633 | EA License Number: 17C8502
