Global CSV Expert OT
St .Prex, Switzerland
vor 4 Tg.

Headquartered in Saint-Prex, Switzerland, Ferring Pharmaceuticals is a research-driven, specialty biopharmaceutical group active in global markets.

A leader in reproductive and maternal health, Ferring has been developing treatments for mothers and babies for over 50 years.

Today, over one third of the company’s research and development investment goes towards finding innovative treatments to help mothers and babies, from conception to birth.

The company also identifies, develops and markets innovative products in the areas of urology, gastroenterology, endocrinology and orthopaedics.

Ferring has its own operating subsidiaries in nearly 60 countries and markets its products in 110 countries. For further information on Ferring or its products, visit www. Global CSV Expert OT Your mission : Accountable to deliver an efficient global validation strategy for local and for multi-site project / programme implementation of OT solutions.

Ensure that the validation strategy and roles and responsibilities between global and local functions and personnel are clear in order to answer accurately to any questions from health authorities.

Maintain the validated status of global OT solutions. Main responsibilities :

  • Maintain the validated status of global OT Systems and Applications with the system owner(s) and the local CSV experts.
  • Ensure that Computer System Validation related CSOPs are understood and implemented for OT Systems and Applications. Any required changes to the existing validation approach for OT Systems and Applications must be carried out (i.
  • e. : updating existing documentation or adding new documents according to a change in the related CSOPs). Work with the authors of the CSOPs to ensure that any specific validation requirements covering the implementation and operation of OT Systems and Applications is considered.

  • Accountable to define the validation strategy for new global OT project implementations and upgrades, ensuring easy ongoing maintainability for routine changes or where changes are expected to be more frequent (i.
  • e. : splitting the validation documentation for each interface and for each custom-made user screen).

  • Responsible to create the global CSV documents templates to support new OT project implementations according to the validation strategy and provide support to local CSV experts whenever required during global project execution.
  • Ensure that the validation documentation and the structure of global OT Systems and Applications are well understood by the manufacturing sites, so they can be independent during health authority audits.
  • Enforce the use of electronic systems for testing (i.e. : RQM) and ensure similar testing structure among projects. Where applicable enforce and support the regression testing using automated testing tools.
  • Participate in the assessment of system reviews, deviations, CAPA, Changes, continuous improvement and troubleshooting related to Global OT Systems and Applications.
  • Establish and lead the process / framework to monitor compliance adherence of OT Systems and Applications both globally and locally with the sites.
  • Responsible to create and maintain through the entire lifecycle the list of GMP OT applications with their compliance condition

  • Guide and support sites during health authority inspection as required, e.g. describing the validation approaches across multiple sites, expert input into questions related to CSV, etc.
  • Required Experience & Competences :

  • Bachelor's degree with a preference in Computer Science or related field. Master’s degree preferred
  • Min 10 years’ experience in an operational IT / OT / Automation position with a good understanding of pharma, chemistry, food industry within industrial company
  • Min 5 years of experience of CSV projects and computer validation methodologies.
  • Min 5 years of experience in writing, reviewing and executing CSV documentations (IQ, OQ, PQ)
  • Strong analytical & problem-solving skills
  • High commitment and result oriented
  • Good communication, good leadership, organised & proactive approach
  • Teamwork and customer oriented
  • Very good knowledge of PLC, SCADA, Historian, Data Collector implementation
  • Fluency in English, other languages will be a plus
  • Information for Recruitment Agencies :

    Ferring as well as all related entities (in the following Ferring) do not accept any candidate submission from unsolicited third parties.

    Candidates presented by unsolicited third parties (such as recruitment agencies, head hunters etc.), will not be entered into the recruitment process and will not be considered further.

    Further on, no contractual relationship will result out of such a submission between Ferring and a third party. Ferring is not obligated nor willing to pay any fee to third parties submitting candidates in this manner.

    Data Processing :

    Ferring (the Group) are proud to be an equal opportunities employer. We are committed to providing equal access to employment opportunities to all prospective employees within the recruitment process.

    The Group complies with and supports all national and local laws pertaining to non-discrimination. Please note that the Group is supported by Serendi for Talent Acquisition Services.

    As their Recruitment Process Outsourcing provider Serendi is exclusively in charge of the above-mentioned position. Your data is handled according to the compliance guidelines of the Group.

    Please see the for more information. If you have any questions your recruiter will be happy to help. (Serendi SA, Avenue de la Gare 2, CH-1700 Fribourg)

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