Pharma Production Manager - NPI & Process Excellence

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

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.

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