QA Specialist – Pharmaceutical Manufacturing

Pengiklan Anonim; Jakarta Timur; On-site; IDR 144,000,000 - 216,000,000; Full time

Benefits offered by this job

Competitive compensation package

Career development opportunities

Job summary

PT Nellco Indopharma seeks a dedicated Quality Assurance Specialist to join our East Jakarta quality management team. You will ensure all pharmaceutical products and processes meet stringent quality standards, regulatory requirements, and industry best practices, safeguarding product integrity and patient safety.

Responsibilities include implementing QC procedures, analyzing test results, and supporting regulatory inspections.

Qualifications

• 3–5 years of QA/QC experience in pharmaceutical manufacturing or related industry.
• Solid knowledge of pharmaceutical regulations, GMP, and quality management systems.
• Laboratory testing techniques and analytical methods for pharmaceutical products.

Responsibilities

• Conduct quality inspections and testing of pharmaceutical products across production stages to ensure compliance with standards.
• Develop, implement, and maintain QC procedures and documentation for pharmaceutical manufacturing.
• Analyze test results, identify deviations, and initiate corrective actions as needed.
• Monitor production processes to identify quality risks and implement preventative measures.
• Collaborate with production, R&D, and regulatory teams to ensure GMP adherence.

Skills

Quality assurance

GMP knowledge

ISO 9001

Laboratory testing

Statistical analysis

Bilingual Indonesian/English

Independent collaboration

Education

Apothecary degree

Tools

Quality management software

Job description

PT Nellco Indopharma seeks a dedicated Quality Assurance Specialist to join our East Jakarta quality management team. You will ensure all pharmaceutical products and processes meet stringent quality standards, regulatory requirements, and industry best practices, safeguarding product integrity and patient safety.

Responsibilities include implementing QC procedures, analyzing test results, and supporting regulatory inspections.