Commissioning & Qualification Specialist

vor 1 Tag


Bern, Bern, Schweiz Randstad Vollzeit
Job Description

We are seeking a highly skilled Commissioning & Qualification Specialist to join our team at Randstad. The ideal candidate will have a strong background in engineering and technical services, with a minimum of 5 years of experience in a C&Q/CQV equivalent position within the pharma industry.



Key Responsibilities:

  • Develop and implement Commissioning & Qualification plans and protocols for new or modified GMP utilities, facilities, and process equipment.
  • Conduct DQ, IQ, OQ, and PQ activities, including protocol deviations, investigation, and corrective action activities.
  • Coordinate and execute FAT/SAT, commissioning activities for new GMP systems in collaboration with internal and external partners.
  • Prepare, review, and approve technical and GMP-related documentation.



Requirements:

  • Bachelor's or Master's degree in Engineering, technical, or natural sciences.
  • Minimum 5 years of working experience within the pharma industry in a C&Q/CQV equivalent position.
  • Knowledge of Qualification requirements according to cGMP regulations.
  • Excellent communication and analytical skills.



Working with us:

We offer a dynamic and challenging work environment, with opportunities for professional growth and development. If you are a motivated and experienced professional looking for a new challenge, please submit your application.



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