Global Director, Oral Solids Manufacturing Tech

Gr?nenthal GmbH

Santiago

Sur place

CLP 90 000 000 - 150 000 000

Plein temps

14 jours+

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Avantages offerts par ce poste

Mobile work

Résumé du poste

Grünenthal is seeking a Global Director Oral Solids Manufacturing Technology (m/f/d) for its Santiago, Chile site. You will lead manufacturing technology, drive scale-up, process transfers and continuous improvement across the network.

You will ensure GMP compliance and regulatory alignment while fostering cross-site collaboration and training initiatives. You bring 10–15+ years in pharmaceutical operations with expertise in granulation, blending, compression, coating, and process validation.

Qualifications

  • 10–15+ years in pharmaceutical operations or technical manufacturing.
  • Expertise across multiple dosage forms, especially oral solids.
  • Strong GMP and regulatory knowledge.
  • Experience with technology transfers and global harmonization.

Responsabilités

  • Provide deep technical expertise in granulation, blending, compression and coating.
  • Lead process validation and troubleshooting across the network.
  • Support technology transfers, scale-up and new product introductions.
  • Drive continuous improvement and harmonization of manufacturing processes.
  • Ensure GMP compliance and regulatory alignment in all activities.
  • Lead investigations and root-cause analyses for complex manufacturing issues.

Connaissances

Granulation
Blending
Compression
Coating
Process validation
Process industrialization
Scale-up
Technology transfers
Lean Six Sigma
GMP compliance

Formation

Chemical Engineering
Pharmaceutical Technology
Process Engineering
Industrial Engineering

Description du poste

Grünenthal is seeking a Global Director Oral Solids Manufacturing Technology (m/f/d) for its Santiago, Chile site. You will lead manufacturing technology, drive scale-up, process transfers and continuous improvement across the network.

You will ensure GMP compliance and regulatory alignment while fostering cross-site collaboration and training initiatives. You bring 10–15+ years in pharmaceutical operations with expertise in granulation, blending, compression, coating, and process validation.

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