- Ensure line clearance & cleaning checks of the batch manufacturing process
- Reviews documentation associated manufacture of products on the manufacturing area during production.
- Work closely with manufacturing to address any production issues on shift and ensure appropriate documentation.
- Coordinates and assembly of batch record documentation to assist with disposition.
- Reviews and approves completed manufacturing related documents for batch record disposition.
- Performs in process control sampling, testing and inspection (as AQL) for all Rameda and Toll Products.
- Coordinates activities associated with deviation report and CAPAs to facilitate investigations and assure timely closure.
- Ensures adherence of appropriate cGMP regulations and quality standards.
- Perform or support any other tasks necessary to maintain the product quality and site cGMP compliance, as needed.
- Ensures that all activities in his unit or section are done according the relevant cGMP and ISO standards (ISO 9001, ISO 14001, OHSAS 18001).
1-3 years of experienceBachelor degree of pharmacy or Science