IPC Specialist At Rameda pharmaceutical company
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 experience
Bachelor degree of pharmacy or Science