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Senior CQV Specialist

vor 1 Monat


Bern, Bern, Schweiz Consultys Vollzeit
Job Summary

We are seeking a highly skilled Senior CQV Specialist to join our Consultys team. As a key member of our C&Q team, you will be responsible for ensuring that CQV activities are executed in accordance with the C&Q Plan and supporting Validation Plans.

Key Responsibilities
  • Lead and coordinate the CQV execution effort supported by C&Q EPC teams, Engineering, Operations, and external vendors and contractors.
  • Plan and schedule commissioning activities according to the C&Q strategy and supporting Validation Plans.
  • Support the updates of Master C&Q Plan and supporting plans during project execution lifecycle.
  • Coordinate the planning and scheduling of commissioning activities with the construction interface and with other disciplines.
  • Guide the C&Q documentation preparation effort to ensure correctness, completeness, and alignment across different areas/systems.
Requirements
  • University degree in Engineering, Chemistry, or another relevant discipline.
  • At least 1 year of experience in Qualification and Validation of equipment.
  • Applied technical understanding of manufacturing or laboratory equipment; processes specific to Pharmaceutical manufacturing preferred.
  • Applied Knowledge of creation and verification of qualification equipment plans (FAT/SAT/DQ/IQ/OQ/PQ).
  • Analytical and structured working style; strong attention to detail.
  • Ability to effectively work as part of a multidisciplinary, international team.
  • Hands-on personality, with flexibility and dedication to maximize our client's value.
  • Fluency in English is required, German or French would be a plus.