Production Manager

Sanofi; Teramo; In loco; EUR 14.000 - 29.000; Tempo pieno

Descrizione del lavoro

Sanofi in Goa is seeking a seasoned Production Manager to oversee end-to-end production planning, scheduling, and new product transfers to the Goa site. You will lead cross-functional teams to meet production plans, maintain WIP, and ensure compliant manufacturing and documentation.

The role demands strong leadership, data-driven process improvements, GMP/cGMP adherence, and staff development to deliver reliable medicines.

Competenze

• Minimum 10+ years of pharma manufacturing experience (OSD).
• Strong knowledge of GMP/cGMP and quality regulations.
• Experience leading large cross-functional teams and budgeting.
• Proficiency with data analytics tools and SAP BOM handling.
• Excellent communication and strategic thinking.

Mansioni

• Plan and schedule production across centers; coordinate with supply chain and cross-functional teams.
• Monitor daily production activities, changeovers, and maintain WIP; document products manufactured.
• Lead New Product Introduction at Goa: transfer from mother plant, BOM prep, SAP recipe creation, batch scheduling, reporting, approvals, and product registration.
• Train and develop staff to implement GMP/HSE, aiming for zero LTI/IWLT.
• Drive process improvements to reduce cycle time, improve yields and capacity utilization.
• Ensure cGMP systems and data integrity; documentation practices, validation status, SOPs; periodic training.

Conoscenze

GMP / cGMP

Lean manufacturing

Leadership

Budgeting

Data analytics

SAP recipes

BOM handling

Cross-functional collaboration

Quality regulations

Communication

Formazione

Bachelor or Master of Pharmacy or MSc

Strumenti

GxP systems

Validation systems

Descrizione del lavoro

As Production Manager at Sanofi in Goa, you will oversee end-to-end production planning, scheduling, and new product transfers to the Goa site. You will work with cross-functional teams to meet production plans, maintain WIP, and ensure compliant manufacturing and documentation. You will lead process improvements, GMP/HSE adherence, and staff development to drive consistent, high-quality output. This role offers impact through scalable operations and cross-site collaboration to deliver reliable medicines.

• Plan and schedule production and allocate work across centers; coordinate with supply chain and cross-functional teams
• Monitor daily production activities, changeovers, and maintain adequate WIP; document all products manufactured
• Lead New Product Introduction at Goa: transfer from mother plant, BOM prep, SAP recipe creation, batch scheduling, reporting, approvals, and product registration
• Train and develop staff to implement GMP/HSE, aiming for zero LTI/IWLT and workforce development
• Drive Process Excellence initiatives to reduce cycle time, improve yields and capacity utilization; review process parameters and quality metrics
• Ensure cgmp systems and data integrity: GMP adherence, quality system implementation, documentation practices, validation status, SOPs; periodic training of personnel
• HSE compliance: adhere to health, safety and environmental policies and requirements
• 10+ years of pharma manufacturing experience (OSD)
• Bachelor or Master of Pharmacy or Master of Science
• Strong production and operations management with KPI and budgeting experience; lean and supply chain knowledge
• Thorough knowledge of EHS, cGMP and quality regulations
• Experience managing medium to large teams; change management exposure; unionized workforce handling
• Experience in cross-functional roles (Quality, Opex, Engineering, Maintenance) is a plus
• Proficiency with data analytics tools and digital systems
• Effective communication
• Negotiation and influencing skills
• Strategic thinking
• SAP recipe creation and BOM handling
• GMP/cGMP and quality systems
• Good Documentation Practice (BMR, BPR, logbooks)