Quality Control (QC) Manager
About the role
As the Quality Control (QC) Manager at PT Medifarma Laboratories', you will be responsible for overseeing the quality control processes and procedures to ensure the consistent production of high-quality pharmaceutical products. This full-time role is based in Depok, West Java and is a critical position within the organisation, directly contributing to the company's overall quality Control and regulatory compliance.
What we're looking for
1. Quality Control Manager is a registered Pharmacist.
2. 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, CPOB.
3. Have leadership skills.
4. Have good command of English.
What you'll be doing
1. Manage all available facilities and existing human resources to optimize the output of the QC Department.
2. Directing the implementation of tasks in the Chemistry and Microbiology Laboratory according to Good Laboratory Practices.
3. Make an annual budget plan and manage QC Department expenses to be balanced and efficient.
4. Support the implementation of best practices at PT Medifarma Laboratories.
5. Make a QC Department monthly report.
6. Conduct training and skills development for employees and conduct annual evaluations of all employees under it.
7. Having commitment to support quality and halal policy in PT. Medifarma Laboratories.
8. Responsible for passing or rejecting raw materials, packaging materials, bulk products and finished products made.
9. Responsible for carrying out chemical and microbiological examinations following valid and approved methods and using materials and equipment that meet specifications.
10. Responsible for carrying out inspection of raw materials, packaging materials have been implemented according to the SOP.
11. BResponsible for carrying out the development of analytical methods for raw materials, development of packaging and packaging materials.
12. Together with the Head of Quality Assurance, Production Manager and Engineering Manager in environmental monitoring and control of drug manufacturers.
13. 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.
14. Responsible for conducting inspection, investigation and sampling necessary for the determination of factors that may have an impact on product quality.
15. Conduct studies and approve validation documents and analysis procedures.
16. Conduct studies and provide approval for documents related to the development of raw materials and packaging materials.
17. Ensure that the implementation of Occupational Safety and Health (K3) is in accordance with applicable statutory procedures and regulations.
What we offer
At PT Medifarma Laboratories', we are committed to providing a rewarding and supportive work environment for our employees. In addition to a competitive salary, we offer a range of benefits, including:
Comprehensive health and life insurance coverage
Opportunities for professional development and career advancement
A collaborative and inclusive company culture
If you're ready to take on a challenging and rewarding role as the Quality Control (QC) Manager at PT Medifarma Laboratories', we encourage you to apply now.
Profil perusahaan
Medifarma Laboratories is a pharmaceutical company based in Indonesia and an affiliate of United Laboratories, Inc., the biggest pharmaceutical company in the Philippines and a sister company of Darya-Varia Laboratoria, Indonesia. With its head office in Depok, on the southern outskirts of Jakarta, Indonesia’s capital, the Medifarma production facility is located in a complex that houses such big-name multinational pharmaceutical companies as Bayer Health Care, Glaxo Smith Kline, Pfizer, etc. Founded in 1975, our original production facility extended to 36,595 m2. It was expanded by 14,164 m2 in 1992 in line with the company’s growth so as total floor space is currently 50,759 m2. Our production facility and operations have been certified by the Indonesia NADFC (National Agency of Drug and Food Control), with standards of manufacturing practice found to be in accordance with the current standard of Good Manufacturing Practices as well as to meet the standard required by Pharmaceutical Inspection Co-operation Scheme (PIC/s) and World Health Organization (WHO). Medifarma exports its products to affiliates in the Philippines, Singapore, Malaysia, Hong Kong, Myanmar and Cambodia. We are committed to maintaining the highest quality standards for everything we produce
101-1,000 employees
Medifarma Laboratories is a pharmaceutical company based in Indonesia and an affiliate of United Laboratories, Inc., the biggest pharmaceutical company in the Philippines and a sister company of Darya-Varia Laboratoria, Indonesia. With its head office in Depok, on the southern outskirts of Jakarta, Indonesia’s capital, the Medifarma production facility is located in a complex that houses such big-name multinational pharmaceutical companies as Bayer Health Care, Glaxo Smith Kline, Pfizer, etc.