CSV Validation Specialist

il y a 3 semaines

Toulouse, Occitanie, France Optimus Life Sciences Temps plein
Job Title: CSV Engineer

We are seeking an experienced CSV Engineer to join our team at Optimus Life Sciences. As a CSV Engineer, you will be responsible for ensuring the validation of computerized systems in the biopharmaceutical sector.

Responsibilities:
  • Validate process control systems, spreadsheets, and benchtop equipment to ensure compliance with regulatory requirements and corporate standards.
  • Develop project scopes, implementation plans, and tracking mechanisms to ensure efficient operations of the CSV department.
  • Collaborate with engineering, controls, IT, and other departments to evaluate new applications and determine validation requirements.
  • Implement continuous improvements to clients' policies, procedures, and local VMPs to ensure efficient operations of the CSV department.
  • Address CSV issues to identify and resolve GMP concerns as the representative or conduit for the Validation Manager.
Requirements:
  • 5-10 years of experience working in CSV functions.
  • Experience working within the pharmaceutical industry under GMP requirements.
  • Ability to work in a team and good communication skills.
  • Fluent in English, French or Dutch skills would be a plus.
What We Offer:

We offer a competitive salary and benefits package, as well as opportunities for professional growth and development.

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