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CSV Engineer

  1. East Anglia
Toulouse
  1. Contract
Competitive
  1. CAPEX Projects
07-08-2024
34760

This vacancy has now expired

CSV Engineer - LIMS implementation - Empower implementation - 12-Month Contract

Our client, a global biotechnology organisation, is recruiting for a CSV to join their capital project in the South of France. This new build facility will house a therapeutic protein production plant, and we are looking for a CSV to help expand our client's biotech operations throughout Europe. As the CSV you will be responsible for implementing all safety requirements for a new build facility, estimated at approximately 14,900m2.


Responsibilities: 
  • Develop and execute validation protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), for computer systems and software applications.
  • Collaborate with cross-functional teams, including IT, Quality Assurance, and Operations, to ensure compliance with regulatory guidelines and internal policies.
  • Perform risk assessments and impact analyses to identify critical system functionalities and potential vulnerabilities.
  • Create and maintain validation documentation, such as validation plans, test scripts, traceability matrices, and validation summary reports.
  • Conduct periodic reviews to ensure ongoing compliance with regulatory requirements and internal procedures.
  • Participate in change control processes, assessing the impact of system changes and ensuring appropriate validation activities are performed.
  • Provide guidance and support to project teams regarding CSV principles, best practices, and regulatory expectations.
  • Stay updated with industry trends, regulatory changes, and advancements in computer system validation practices.

Requirements:
  • Bachelor's degree in Computer Science, Engineering, or a related field.
  • French speaking is an ideal
  • Strong knowledge of regulatory guidelines, such as FDA 21 CFR Part 11, EU Annex 11, and GAMP 5.
  • Experience in computer system validation within a regulated industry, preferably pharmaceuticals or biotechnology.
  • Familiarity with validation methodologies, including risk-based validation approaches.
  • Proficiency in creating and executing validation protocols and documenting validation activities.
  • Excellent analytical and problem-solving skills, with attention to detail.
  • Strong communication and interpersonal skills to collaborate effectively with cross-functional teams.
  • Ability to work independently and manage multiple projects simultaneously.


If this role is of interest to you, please apply now! 

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