Global Director, Oral Solids Manufacturing Tech

Grünenthal Group

Santiago

À distance

CLP 30 000 000 - 60 000 000

Plein temps

Il y a 39 heures
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Résumé du poste

Grünenthal Group is seeking a senior professional for Manufacturing & Global Operations to drive process engineering and technology transfers across the network. You will support scale-up, troubleshoot complex manufacturing issues, and ensure GMP compliance while maintaining product quality and regulatory standards.

The role requires 10–15+ years in pharmaceutical operations with hands-on expertise in oral solids and multiple dosage forms.

Qualifications

  • 10–15+ years of experience in pharmaceutical operations, process engineering, or technical manufacturing.
  • Academic background in Chemical Engineering, Pharmaceutical Technology, Process Engineering, Industrial Engineering.
  • Hands‑on expertise across multiple dosage forms and technologies, especially oral solids.
  • Experience leading technology transfers and scale‑up between development, sending and receiving sites.

Responsabilités

  • Provide deep technical expertise in granulation, blending, compression, coating, and process validation.
  • Support new product introductions, process transfers, and scale-up activities.
  • Lead complex manufacturing investigations and root cause analyses.
  • Translate process science into high-scale production respecting GMP and regulatory requirements.
  • Serve as the technical authority for manufacturing processes network-wide, focused on oral solids.

Connaissances

Process engineering
Technology transfers
GMP knowledge
Lean Six Sigma
Root cause analysis

Formation

Chemical Engineering or related field
Industrial Engineering background

Description du poste

Grünenthal Group is seeking a senior professional for Manufacturing & Global Operations to drive process engineering and technology transfers across the network. You will support scale-up, troubleshoot complex manufacturing issues, and ensure GMP compliance while maintaining product quality and regulatory standards.

The role requires 10–15+ years in pharmaceutical operations with hands-on expertise in oral solids and multiple dosage forms.

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