Quality Assurance Specialist, Documentation

About the role You will manage GMP documentation and records throughout their full lifecycle. Acting as the guardian of data integrity, you will ensure that all technical documents, including batch records and SOPs, are properly created, tracked, and archived. Location : Tuas Biomedical Park with company shuttle bus provided islandwide Job Responsibilities: Oversee the implementation and maintenance of document management systems and processes. Administer the MasterControl electronic system, ma…