- Conduct quality audits to ensure compliance with ISO standards and company policies.
- Review and approve quality documents, including IMS (Integrated Management System) documentation.
- Develop and implement effective quality control processes to maintain high-quality products and services.
- Collaborate with cross-functional teams to identify areas for improvement in the quality management system.
Job Requirements :
- 3-6 years of experience in a similar role within the chemical industry.
- Solid understanding of ISO documentation requirements for medical devices manufacturing.
- Excellent documentation skills, including attention to detail and ability to review complex technical documents.