Review and approve master batch records and completed batch records for the manufacture, packaging, and labelling of intermediates and active pharmaceutical ingredients (APIs), ensuring compliance with Pfizer quality standards and registered regulatory specifications.
Define test strategies, plans, and release criteria for internal AI products. Prioritise coverage based on user impact, data sensitivity, and product risk.
Role Summary: Supports the production and quality control departments by managing daily administrative work, tracking output and wastage, filing inspection records, and coordinating cross-departmental workflows.
Develop a good understanding of the Government ICT environment, key developments and growing trends relevant to Government ICT audits (e.g., control requirements in the Government Instruction Manual on ICT&SS Management, use of cloud computing, greater automation of processes, block chain technology, etc.)