Supervisor QC WIP & FG

Selamat Datang di Situs Lowongan Kerja Indonesia Terbaru 2026 dan Saat ini kami ingin memberitahukan Info Terbaru Mengenai Informasi Loker dari Perusahaan PT Mersifarma TM dengan posisi Supervisor QC WIP & FG. Untuk selengkapnya silahkan baca deskripsi lowongan kerja di bawah ini dengan seksama dan teliti, beserta persyaratan minimal lowongan kerja di yang telah tertera dan dijelaskan di bawah ini.

PT Mersifarma TM melalui program rekrutmennya saat ini sedang membuka lowongan kerja untuk posisi Supervisor QC WIP & FG di Sukabumi yang bertujuan untuk meningkatkan kinerja operasional di dalam maupun luar kantor PT Mersifarma TM. Perusahaan Tersebut sedang mencari calon tenaga kerja yang siap diterjunkan ke setiap divisi bagian perusahaan yang sesuai dengan posisi, kemampuan dan keahlian para pencari kerja tersebut. Berikut ini adalah detail lengkap persyaratan untuk posisi Supervisor QC WIP & FG di Sukabumi Perusahaan PT Mersifarma TM:

• Supervise analytical testing activities for Work In Process (WIP), bulk products, and Finished Goods (FG).
• Lead and develop QC Analysts to ensure testing activities are conducted in accordance with approved procedures and GMP/CPOB requirements.
• Review analytical records, laboratory documentation, and test reports to ensure accuracy and compliance.
• Monitor laboratory operations, including logbooks, controlled substances, working standards, and analytical equipment utilization.
• Investigate deviations, OOS/OOT results, and support CAPA implementation.
• Collaborate with Production, QA, and other stakeholders regarding product quality and testing status.
• Review and improve analytical methods, SOPs, and laboratory practices.
• Prepare periodic reports and support internal/external audits and regulatory inspections.
• Ensure compliance with safety, environmental, and quality management requirements.

Job Qualifications:

• Bachelor’s Degree in Pharmacy, Chemistry, Pharmaceutical Sciences, or related fields.
• Pharmacist (Apothecary) certification is an advantage.
• Minimum 5 years of experience in Pharmaceutical Quality Control, with prior supervisory experience preferred.
• Strong understanding of GMP/CPOB, Deviation Management, CAPA, Validation, Qualification, Calibration, Risk Management, and Internal Audit Systems.
• Hands-on experience with analytical instruments such as: HPLC, GC, UV-Vis Spectrophotometer, FTIR, Karl Fischer, ICP-OES, Dissolution Tester, and other laboratory analytical equipment.
• Strong leadership, communication, teamwork, and problem-solving skills.
• Proficient in Microsoft Office applications.