Alza Pharmaceuticals is seeking a dynamic and experienced Production Manager to lead our end-to-end manufacturing operations. We are looking for a leadership-oriented professional with extensive hands-on experience in both sterile and non-sterile pharmaceutical production. The ideal candidate will drive operational excellence while ensuring the highest standards of quality and regulatory compliance.
Operations Management: Oversee and supervise the entire production lifecycle for a diverse range of sterile and non-sterile products.
Planning & Execution: Drive effective production planning and scheduling to meet institutional targets and optimize resource utilization.
cGMP Compliance: Ensure 100% adherence to cGMP requirements, Standard Operating Procedures (SOPs), and safety protocols.
Process Optimization: Continuously analyze and improve manufacturing workflows to minimize losses and enhance cost-effectiveness.
Cross-Functional Coordination: Collaborate closely with Quality Assurance (QA) and Quality Control (QC) to maintain product integrity.
Regulatory Support: Lead and manage regulatory affairs support, including preparation for inspections and internal/external audits.
Leadership: Train, mentor, and motivate production teams to achieve high performance and operational excellence.
Education: B. Pharmacy / Pharm-D or a relevant advanced degree.
Experience: 12 to 15 years of experience in pharmaceutical production, with several years in a managerial capacity.
Product Exposure: Proven expertise in Sterile & Non-Sterile products (Ophthalmic experience is highly preferred).
Technical Knowledge: Strong understanding of Medical Devices Manufacturing and equipment handling.
Industry: Pharmaceutical Manufacturing.
Manufacturing Excellence: In-depth knowledge of pharmaceutical manufacturing operations and sterile suite management.
Regulatory Mastery: Sound understanding of cGMP, SOPs, and DRAP regulatory requirements.
Leadership: Exceptional team management and conflict-resolution skills.