Bioprocess Equipment Engineer for GMP & CQV

Sandoz France

Toulouse

Sur place

EUR 70 000 - 90 000

Plein temps

14 jours+
Générateur de candidature

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Résumé du poste

Sandoz France is seeking a Manufacturing Equipment Engineer to support a biopharmaceutical facility project in Toulouse. You will own equipment life cycle, support process control, and drive maintenance planning. You will participate in CQV activities (IOQ/PQ) and document SOPs, procedures and batch reports.

Fluent English and French communication, plus hands-on experience with qualification and GMP processes, are essential in this collaborative, agile culture.

Qualifications

  • Master or Engineer degree in engineering/biotech or related field.
  • 3+ years of relevant experience in a similar role.
  • Fluent in English and French, both written and spoken.

Responsabilités

  • Support Manufacturing Operations with process control expertise.
  • Act as equipment owner, ensuring life cycle management of equipment.
  • Support investigations, CAPA and changes related to process equipment.
  • Contribute to CQV activities (IOQ and PQ) with USP/DSP process knowledge.
  • Assist manufacturing in troubleshooting and improvement projects.
  • Define and execute equipment maintenance plans in alignment with Maintenance planner.
  • Create and review technical docs like SOPs, work procedures and batch reports.

Connaissances

Process equipment
Equipment commissioning
Equipment validation
cGMP knowledge
GMP documentation
FMEA
Data analysis
Bilingual EN/FR
Automation recipes
Troubleshooting
Single-use systems
Team collaboration

Formation

Master or Engineer in engineering/biotech

Description du poste

Sandoz France is seeking a Manufacturing Equipment Engineer to support a biopharmaceutical facility project in Toulouse. You will own equipment life cycle, support process control, and drive maintenance planning. You will participate in CQV activities (IOQ/PQ) and document SOPs, procedures and batch reports.

Fluent English and French communication, plus hands-on experience with qualification and GMP processes, are essential in this collaborative, agile culture.

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