Job Description
Full details about the role and requirements
Yukerja Summary
The QC Chemical Supervisor role at Anvita Pharma Indonesia is curated from JobStreet (category Teknologi & IT). Note the work location (Karawang, West Java) before applying. Yukerja.com is not the employer — applications are handled on the official source site.
Requirement:
Bachelor Degree of Pharmacy / Chemistry / Industry / related fields (Aphothechary Competency Certificate is a plus)
≥ 2 years experience in the field of QC in the Pharmaceutical Industry
Have deep knowledge of QC in the Pharmaceutical Industry
Have skill in Standard procedures for quality control in the GMP/CPOB corridor for the pharmaceutical industry set by the Ministry of Health and BPOM; Quality Management System; GMP [CPOB], GDP [Good Documentation Practice] and GLP [Good Laboratory Practice]; Laboratory equipment/instrument used in the pharmaceutical industry; pharmaceutical chemical analysis; Root cause analysis
Have skills in using MS. Office & Excellent skill in English
Jobdesc :
Supervise and evaluate the stages of analysis terms of HSE, Quality and Compliance in the QC Chemical area
Plan and ensure the use of machines/instruments, equipment, stock materials and consumables required to carry out activities and compliance in the QC Chemical area
Creates SOPs, protocols, and working instruction that are relevant to validation needs, routine activities, and each project plan
Create specifications and analysis methods as needed
Create URS documents as needed
Supervising the use of machines/instruments, equipment, machines/instruments change parts, stock of materials and other consumables; and also ensure its readiness
Planning and scheduling the activities of the Analyst and Inspectors
Create, review, assess and determine the impact of proposed changes relating to and relating to products, facilities and machines/instruments in QC Chemical area
Coordinate cross-functionally with QA, Production, Engineering, and Supply Chain to ensure effective planning and execution of sampling activities, calibration, qualification, environmental monitoring, as well as maintenance, repair, and spare part management for machines and instruments in the QC Chemical area.