Quality Control; Qc) Supervisor

Bachelor’s Degree in Pharmacy with a valid Pharmacist Professional Degree (Apoteker).

Minimum 3–5 years of experience in Quality Control within the pharmaceutical industry.

Previous experience as a QC Supervisor or in a similar leadership position is an advantage.

Strong knowledge of Good Manufacturing Practices (GMP/CPOB), pharmacopoeial standards, and pharmaceutical quality control procedures.

Familiar with testing raw materials, packaging materials, in-process materials, bulk products, and finished products.

Proficient in operating laboratory instruments such as HPLC, GC, UV-Vis Spectrophotometer, and other analytical equipment.

Knowledge of Softgel Capsule testing, gelatin quality testing, and pharmaceutical product specifications is an advantage.

Understanding of analytical method validation, OOS/OOT investigations, CAPA, and product stability studies.

Strong leadership, analytical thinking, problem-solving, and decision-making skills.

Detail-oriented, disciplined, responsible, and able to work effectively both independently and as part of a team.

Supervise and ensure all QC testing activities for raw materials, packaging materials, in-process materials, bulk products, and finished products are performed according to established specifications and procedures.

Ensure the quality testing of Softgel Capsule products meets applicable quality standards and specifications.

Monitor laboratory activities, including sampling, testing, documentation, and reporting of analytical results.

Ensure laboratory equipment is properly maintained, calibrated, qualified, and fit for use.

Coordinate investigations of Out of Specification (OOS), Out of Trend (OOT), and other laboratory deviations, including the implementation of appropriate CAPA.

Supervise product stability studies and retain sample management in accordance with applicable procedures.

Ensure compliance with GMP/CPOB requirements, internal SOPs, and applicable pharmaceutical regulations.

Lead, coordinate, and evaluate QC team performance, including task assignments, training, and competency development.

Support internal and external audits, regulatory inspections, and continuous quality improvement initiatives.

Coordinate with QA, Production, R&D, PPIC, and other relevant departments to ensure product quality and compliance.

Prepare and submit periodic QC activity reports to management.

Pharmaceuticals, Biotechnology & Medical Devices 51-100 employees

PT. Nova Chemie Utama is a company engaged in pharmaceutical industry particularly in manufacturing softgel capsule.

PT. Nova Chemie Utama has received quality standard and BPOM certification.

We have complete facilities supported with appropriate technology to produce quality products in accordance with consumer needs.

In addition to softgel capsule manufacturing, we provide services related to product development and analysis facilitated with complete laboratories and supported with experts in particular fields. Our commitment is to give an excellent service.

PT. Nova Chemie Utama is a company engaged in pharmaceutical industry particularly in manufacturing softgel capsule.

PT. Nova Chemie Utama has received quality standard and BPOM certification.

We have complete facilities supported with appropriate technology to produce quality products in accordance with consumer needs.

In addition to softgel capsule manufacturing, we provide services related to product development and analysis facilitated with complete laboratories and supported with experts in particular fields. Our commitment is to give an excellent service.