QC Supervisor

PT Taisho Pharmaceutical Indonesia Tbk.; Depok; On-site; IDR 290,160,000 - 513,360,000; Full time

Job summary

PT Taisho Pharmaceutical Indonesia Tbk. seeks a QC professional to supervise analysis of in-process, finished products and raw materials, ensuring GMP, GLP, and EHS compliance.

Requirements: Bachelor’s degree in Pharmacy with at least 5 years in pharmaceutical quality control; strong chemical testing and instrumental analysis skills; good English and computer proficiency. Responsibilities include coordinating analyses, supporting material releases with the QC APJ, sampling, maintaining QC

Qualifications

• Bachelor’s degree in Pharmacy required.
• Minimum 5 years in pharmaceutical quality control.
• Proficient in chemical testing, instrumental analysis, and English.
• Good computer skills.

Responsibilities

• Coordinate analyses of in-process, finished products and raw materials; ensure GMP, GLP, and EHS compliance.
• Schedule analyses and support for material releases with the QC APJ; manage sampling.
• Maintain QC documentation and supervise QC staff; conduct OOS investigations; ensure GLP training.

Skills

Chemical testing

Instrumental analysis

English language

Computer skills

Education

Bachelor's degree in Pharmacy

Job description

Supervise the analysis of in-process products, finished products, and raw materials, ensuring compliance with validated procedures, quality standards, and GMP requirements, while ensuring all analytical instruments and equipment are properly calibrated.

Key responsibilities

Schedule and coordinate the analysis of finished products and raw materials

Provide backup support for the release of raw materials, packaging materials, and finished products in coordination with the QC Authorized Person (APJ QC)

Oversee the collection of representative samples, as well as the preparation and maintenance of quality control documentation for the chemical laboratory

Ensure that testing results meet applicable testing standards, GMP and EHS requirements, as well as established Key Performance Indicators (KPIs)

Establish and implement procedures in accordance with Good Laboratory Practices (GLP)

Conduct laboratory investigations in case of out-of-specification (OOS) results

Prepare analytical method validation protocols and reports for raw materials

Ensure compliance with applicable safety regulations and requirements within the Quality Operation Department

Develop training methods and materials and provide GLP training to relevant personnel

Supervise and evaluate Quality Control personnel to ensure effective performance and quality control activities

Experience Requirement

Bachelor's degree in pharmacy

Minimum of 5 years of experience in pharmaceutical quality control

Proficient in chemical testing and instrumental analysis

Good command of computer skills

Good English skills, both verbal and written

Taisho Pharmaceutical Indonesia is the subsidiary of Taisho Pharmaceutical Co., Ltd., Japan - the number one over-the-counter medications company in Japan.

In Indonesia, Taisho Pharmaceutical has been operating since the end of 2009 after acquiring Bristol-Myers Squibb. Our main brands are Counterpain, Tempra, Theragran-M, Kenacort, Myco-Z and Mycostatin OS (Oral Suspension).

Taisho Pharmaceutical Indonesia is the subsidiary of Taisho Pharmaceutical Co., Ltd., Japan - the number one over-the-counter medications company in Japan.

In Indonesia, Taisho Pharmaceutical has been operating since the end of 2009 after acquiring Bristol-Myers Squibb. Our main brands are Counterpain, Tempra, Theragran-M, Kenacort, Myco-Z and Mycostatin OS (Oral Suspension).