Deskripsi pekerjaan
QC Supervisor bertanggung jawab mengawasi analisis produk dalam proses, produk jadi, dan bahan baku untuk memastikan kepatuhan terhadap prosedur tervalidasi, standar kualitas, dan persyaratan GMP. Peran ini memastikan seluruh instrumen analitis dan peralatan laboratorium dikalibrasi dengan benar serta beroperasi sesuai standar Good Laboratory Practices (GLP). Selain pengawasan teknis, posisi ini berperan dalam pengembangan tim, penyusunan protokol validasi metode analitis, dan investigasi laboratorium jika terjadi hasil di luar spesifikasi (OOS). QC Supervisor juga memastikan kepatuhan terhadap regulasi keselamatan dan KPI departemen, serta memberikan pelatihan kepada personel terkait untuk menjaga efektivitas operasional kontrol kualitas.
Tanggung jawab: 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.
Kualifikasi: Bachelor's degree in pharmacy.
Tanggung jawab
- 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
Kualifikasi
- Bachelor's degree in pharmacy
Informasi lowongan
- Tipe pekerjaan
- Full-time
- Pendidikan
- S1
- Gaji
- Negosiasi