Have more technical knowledge in the IPC area (Sampling, testing, controlling, reconcile batch record investigation, product segregation)
Execute all daily in-process control activity during manufacturing process (Production, Effervescent line, Packing and Inspector, including sampling, testing controlling, data entry, Gemba inspection, calibration instrument regular review on Log sheet, Daily verification balance, sanitation room and GMP alarm report) with minimum supervision according with SOP, department objective, GxP requirement and HSE rules
Able to perform training for the new IPC officer (Sampling testing and controlling)
Performing investigation and product impact segregation triggered e.g. by OOS/OOT, complaint and deviation etc.
Execute operation instrument calibration, qualification and Verification (URS, RA, DQ and technical clarification) in coordination with quality department
Execute the effective closure of all corrective and preventive actions by performing investigation and recommendation through Deviation Control
To execute all sample Composite/Stability/MP/Retained for commercial batch is deliver to QC with timely manner
Join on daily tier 1 communication (shift change over) and speak up or report regarding Safety, Quality, Delivery (batch record) and others improvement related with IPC.
Execute tasks within Change Management as a result of process improvement activities, audit finding and general review process
Support in the GMP Self Inspection, 5S inspection, HSE inspection & internal/external audit by creating action plan activities, timeline and managing effective closure of all findings relevant to GMP Compliance team
Perform complete 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. Ensure responsibility and daily target are followed through to ensure sustainability
Fill out on Log sheet, Daily verification balance, sanitation room and GMP alarm report.
Further, continuously reviews the SOPs used in this field to be up-dated as required to be in line with the up-dated quality guideline and Bayer guideline and monitoring its implementation
WHO YOU ARE
Be familiar with Bayer procedures, cGMP, BPOM regulations, occupational health and safety regulations, and management in relation to Operations of PT Bayer Indonesia.
Well developed communication and proficiency in both Indonesian and English language (verbal and written).
Min have experience in pharmaceutical industries 1 - 2 years/fresh graduate are welcome to apply
Preferable as apothecary/pharmacist, and or Bachelor degree chemists, Micro, Biology.
Application Period:
30/05/2022
Reference Code:
640443
Division:
Consumer Health
Location:
Indonesia : DKI Jakarta Jakarta : Cibubur Jakarta
Functional Area:
Production&Manufacturing
Position Grade:
R010
Employment Type:
Temporary Work
Work Time:
Flexi Hours (8 working hours)
Contact Us
AddressTelephoneE-Mail
PT Bayer Indonesia
Menara Astra, 33rd floor
Jl. Jend. Sudirman Kav.5-6, Jakarta 10220, Indonesia
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