Niveau: Mid-Senior level

Type d’emploi: Full-time

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le contenu du travail

Tasks

  • You actively participate in technology transfer and upscaling projects at CMOs.
  • You represent our client in projects managed by external partners.
  • You collaborate with internal teams, including quality, technical, regulatory, and manufacturing
  • You review and approve validation protocols and reports
  • You monitor timelines, activities, budgets, and ensure regulatory compliance
  • You manage deviations, change control, and CPV (Continued Process Verification)
  • You provide technical support and critical insight on sterile operations, including compounding and filling

Profile

  • You have at least 3 years of experience in sterile pharmaceutical environments, specifically in syringe/vial filling
  • You have expertise in technology transfers
  • You are knowledgeable about validation, deviation management, and CPV
  • You have strong project management skills
  • You exhibit a strong quality mindset
  • You can work effectively with external partners (CMOs).
  • You demonstrate autonomy, integrity, and strong influencing skills.
  • You are fluent in English
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Date limite: 06-01-2026

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MÊMES EMPLOIS

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