Senior Production Manager – GMP & Process Excellence

Sanofi

Teramo

In loco

EUR 14.000 - 29.000

Tempo pieno

4 giorni fa
Candidati tra i primi
Generatore di candidature

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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

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.

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