Key Responsibilities:

• Supervise daily production activities to achieve targets safely and efficiently.
• Ensure GMP compliance, line clearance, and adherence to approved manufacturing procedures.
• Monitor production output, product quality, and equipment utilization.
• Lead, coach, and motivate production personnel.
• Ensure accurate completion of Batch Manufacturing Records (BMRs), SOPs, and production documentation.
• Drive batch reconciliation, CAPA implementation, and continuous improvement initiatives.
• Promote a safe working environment and maintain high-quality standards.

Qualifications and Experience:
Ideal Candidate Requirements

• Bachelor’s degree in chemistry, Industrial Chemistry, Biochemistry, Pharmaceutical Sciences, or a related health science field.
• Minimum of 3 years’ experience in pharmaceutical manufacturing, preferably in tablet manufacturing or formulation and process development.
• Strong knowledge of GMP and pharmaceutical quality systems
• Experience with SAP and Microsoft Office is an added advantage.
• Excellent leadership, communication, and problem-solving skills.