Position: Entry level

Job type: Full-time

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Job content

Job Summary

As Production Engineer, you will join a dynamic team with transversals accountabilities through the sterile production’s department. As the sterile production is increasing, we open this position for someone who can support all current projects and support production activities.

This Position Will Ensure
  • the resolution of Technical Deviation & CAPA
  • to participate to the day-to-day production & technical meetings
  • to participate / Ensure HSE requirements through technical activities
Major Responsibilities
  • Give support to the sterile manufacturing projects
  • Give support to operational activities (management of deviation &CAPA, change control and training)
    • Work with Manufacturing Team (Production; Compliance & Technical Support )
    • Define with local teams (prod, QA, Q&V, ENG, RA)
  • Define with local teams (prod, QA, Q&V, ENG, DEV, RA) the best process validation strategy
  • Write and/or review and/or approve project / production / qualification documentation
Preparation of QA related documentation such as cGMP Process Change Controls. Responsible to assure adherence to cGMP requirements throughout all phases of project execution

Qualifications
  • Bachelor’s Degree Required; preferred area of study, Chemical Engineering, Mechanical Engineering or Bioengineering- Or equivalent experience.
  • Substantial experience in the manufacturing and operation of Biopharmaceutical products, both manufacturing and support systems (cGMP manufacturing).
  • Experience in project management and coordination associated with the execution of capital projects in an industrial environment.
  • Practical experience in the coordination of equipment vendors.
Experience and ability to work with a cross-functional team
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Deadline: 10-01-2026

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