IPC Specialist

Job Description

• 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).

Job Requirements

• 1-3 years of experience
• Bachelor degree of pharmacy or Science