IPC (Contract)

MAJOR TASKS

• Executes all daily in-process control activity during manufacturing process (Production, Effervescent line, Packing including sampling, testing controlling) and reports such any deviation and progress, performs alignment with other department in regards In process control activity relevant.
• Ensures that all instruments in operation department are well maintained and calibrated.
• Executes all sample Composite/Stability/MP/Retained for commercial batch is delivered to QC with timely manner.
• Ensures that the IPC facilities (rooms, instruments, utensils, and other properties) are clean, orderly placed, in its proper validity and good working condition, safety operable and secured.
• Completes timely Batch Records review, reconcile of batch record and closure to meet site KPI target, including daily BR Scrum Board performance dialogue with key stakeholders. Ensures responsibility and daily target are followed through to ensure sustainability.
• OPV & PQR data collection for products produced by Business Unit
• Execute all related to SOPs and master MBRs (Master Batch Record) in Manufacturing Business Unit area according to routine review document, its training, process improvement, audit findings and relevant review process.
• Support to generate and monitor tracking of batch record review lead time. Complete Batch Record reviews in a timely manner and fulfill KPI sites, including conducting daily scrum board discussions with key colleagues. Ensuring daily responsibilities and targets are followed up to ensure sustainability, with involvement from the Manufacturing Risk Control team

SKILLS & REQUIREMENTS

• Minimum of Diploma 3 (D3) / Bachelor's Degree in Pharmacy / Chemistry
• Experience in Pharmaceutical Industry, preferably In Process Control
• New graduates are welcomed to apply
• Familiarity with pharmaceutical industry
• Strong knowledge of In Process Control instruments
• Excellent attention to detail and analytical skills
• Excellent communication and teamwork abilities