Report to: Managing Director
Subordinate: Assistant & Staff
- Building and maintaining the factory quality management system (QMS) according to GMP ASEAN, cGMP, ISO 22716 standards.
- Directing the quality management department to carry out activities to ensure product quality according to the basic standards set by the customer or the company.
- Review and approve product batches to be exported from the factory.
- Resolving product quality problems after shipment.
- Controlling the quality in production process from materials, package to bulk and finished product.
- Manage the laboratory, build the testing manual and standard.
- Responsibility to the Board of Directors for building, maintaining the factory’s QMS according to GMP-ASEAN, cGMP, ISO 22716 standards.
- Managing Quality Management Dept and organizing, implementing QMS’s activities.
- Ensuring the quality of the finished products to meet the standards.
- Evaluating the entire production process (batch records, test sheets, the asessment result of production condition; inspection during production, ect.)
- Deciding export-workshop and responsible for the finished product’s quality after factory.
Qualification: Graduated from University, Master - Major in Pharmacist, Pharmaceutical Chemistry, Organic Chemistry, Biotechnology and other relating majors.
- At least 5 years of similar roles in pharmaceutical, cosmetic, chemical manufacturing factories or similar factories.
- Proficient in laboratory operations: preparation of reagents, standard solutions, sampling for testing, prior experience in color mixing is preferred.
- Fluent in foreign languages (English or Chinese).
- Regarding qualifications, skills, personal abilities and other requirements.
- Ability to develop, evaluate and improve policies and procedures.
- Ability to evaluate test results.
- Self-study and analytical skills.
- Enthusiasm, honesty, work under pressure.
- Ability to work independently, present, communicate well, etc.
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