Production Manager

Sanofi

Firenze

In loco

EUR 90.000 - 120.000

Tempo pieno

4 giorni fa
Candidati tra i primi
Generatore di candidature

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Descrizione del lavoro

Sanofi seeks a Production Manager in Goa to oversee end-to-end production planning, scheduling and new product transfers. 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 scalable operations and reliable medicines across sites.

Competenze

  • Bachelor or Master of Pharmacy or Master of Science required.
  • Experience in pharma manufacturing and cGMP environments preferred.
  • Strong leadership and staff development capabilities.
  • Proficiency with data analytics tools and digital systems.
  • Experience with SAP recipes and BOM management is a plus.

Mansioni

  • Plan and schedule production 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 and drive continuous improvement.
  • Drive Process Excellence to reduce cycle time, improve yields and capacity utilization; monitor KPIs.
  • Ensure cGMP and data integrity; uphold SOPs andQuality systems; provide periodic training.

Conoscenze

Production planning
GMP/cGMP
Data analytics
Leadership
Cross-functional collaboration
SAP

Formazione

Bachelor/Master of Pharmacy or MSc

Strumenti

SAP
BOM handling

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)
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