The first high medical technology facility in Singapore dedicated to clinical research, including the in-house therapeutic production. The clinical research specifically focuses on disease areas relevant to Singapore with the objective that such research should translate into improved healthcare for the general population. In particular, the availability of an advanced therapeutic production facility will enable our centre to perform human studies and participate in an early-stage assessment of new molecules, particularly with pharmaceutical companies developing new treatments.
To support the Quality Assurance team in the day to day operations for the release of investigational radiopharmaceuticals and assist in improving the Quality Management System in compliance with PIC/S GMP.
To assume the duties of the therapeutic production batch release.
1. Primary Document Manager, undertaking all tasks related to the control and management of the documentation, including but not limited to:
• Daily issuance of Batch Manufacturing Records and labels etc
• Issuance of SOPs, protocols, log books, registers etc.
• Control, management and issuance of training programs and records
• Maintaining and improving the overall document management system
2. To support in the management of the supplier management system
3. To support internal and external auditing program
4. Assist in validation management activities
5. Assist in quality assurance related projects
6. To support the trending statistics
7. To assume the duties of the Authorized Person for a release of investigational radiopharmaceutical
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- Company:
CFD Pte. Ltd. - Designation:
Quality Assurance Senior / Junior Executive - Profession:
Healthcare / Pharmaceutical / Sports - Industry:
Manufacturing General / Biomedical / Pharmaceutical