Production Supervisor

• Plan, supervise, and coordinate daily manufacturing, filling, and packaging activities to meet production schedules, yield, and quality targets.
• Ensure production activities comply with GMP/CPOB, SOPs, safety, hygiene, line-clearance, and data-integrity requirements.
• Review batch records, logbooks, checklists, and production documentation for completeness and accuracy before submission to QA.
• Lead, train, and assess Production Staff and operators; manage manpower allocation and support team performance.
• Identify and manage deviations, non-conformities, equipment issues, and production bottlenecks; support root-cause analysis and CAPA with QA.
• Coordinate with PPIC, QA, QC, Engineering, Maintenance, and Warehouse to ensure material availability, equipment readiness, and smooth operations.

• S1 in Pharmacy, Pharmaceutical Sciences, Chemistry, Chemical Engineering, Industrial Engineering, Biology, or a related field; Apoteker certification is an advantage.
• Minimum 3–5 years’ experience in pharmaceutical manufacturing, production supervision, or a related GMP-regulated environment.
• Strong knowledge of GMP/CPOB, SOPs, batch records, line clearance, deviation management, and CAPA.
• Proven experience supervising, training, and leading production operators or junior staff.
• Strong problem-solving, decision-making, leadership, and cross-functional coordination skills.
• Strong English and Bahasa Indonesia communication skills, both written and verbal.
• Willing to work in a manufacturing environment and rotating shifts when required.
• Preferred: experience with solid dosage, sterile products, packaging lines, validation support, or SAP/ERP systems.

• Compensation: Not disclosed

English, Bahasa Indonesia