Have practical experience of at least 5 years working in the Quality Control section of pharmaceutical factories, have experience and knowledge in the fields of analytical chemistry and microbiology, inspection of packaging materials
Responsible, hard worker, fast learner, and strong leadership
Have received training and understand the Good Manufacturing Practices (CPOB)
Have a good command of English
Job Description
Manage all available facilities and existing human resources to optimize the output of the QC Department.
Directing the implementation of tasks in the Chemistry and Microbiology Laboratory according to Good Laboratory Practices.
Responsible for passing or rejecting raw materials, packaging materials, bulk products and finished products made
Responsible for carrying out chemical and microbiological examinations following valid and approved methods and using materials and equipment that meet specifications.
Responsible for carrying out inspection of raw materials, packaging materials have been implemented according to the SOP.
Responsible for carrying out the development of analytical methods for raw materials, development of packaging and packaging materials
Ensure that the samples tested for the stability study program are in accordance with their designation and implemented correctly, in accordance with the approved SOP.
Conduct studies and approve validation documents and analysis procedures.
