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Computer System Validation Lead

Req ID: J2281724

  • Location
    Haegendorf, Solothurn, Switzerland
  • Category Information Technology
  • Posted Thursday, August 5, 2021
  • Time Type Full time
  • Job Type Permanent Employee

Job Description

Job overview

The Computer System Validation (CSV) Lead will report to the Jabil Healthcare Sr. Manager of Computer System Validation and will be responsible for leading, conducting, coaching, or supervising CSV projects within the scope of the Jabil Quality Management System of various sizes and scopes, such as enterprise systems, SaaS, stand-alone applications, and Excel spreadsheets.

This position requires strong collaboration with Quality, Information Technology, and Business Owners. The CSV Lead will participate in supplier assessments and provide support during audits and inspections, such as internal audits, FDA, BSI, etc.


- Coordinates with Business owners and SMEs, IT representatives, and Quality to assess, scope, plan, lead, and complete validations of GxP IT items (applications, systems, spread‐sheets, etc.):

  • Complete validation assessments
  • Participate in business process requirements analysis
  • Author validation plans
  • Review and conduct requirements traceability to design specifications
  • Participate in supplier assessments
  • Author test plans
  • Supervise and lead test development, dry-running, execution, and post-execution review
  • Author validation summary reports

- Review and approve CSV deliverables and activities
- Develop and deliver training in a variety of formats, related to regulatory compliance, quality systems, and validation practices
- Participate in IT change control as a validation representative
- Mentor and coach CSV personnel and participants
- Participate in and support audits and inspections, such as internal audits, FDA, and BSI


  • Strong leadership skills
  • Strong project-management skills
  • Strong regulatory and standards knowledge, such as 21 CFR 820, 21 CFR 11, and ISO 13485
  • Strong computer-science\technical knowledge
  • Strong validation testing knowledge
  • Strong problem-solving skills
  • Strong coaching\mentoring skills
  • Thorough knowledge and understanding of good documentation practices and GxP compliance requirements

Education and Experience :

  • Bachelor’s Degree in Engineering / Technology or related field
  • 10+ years validation related work experience in an FDA regulated environment
  • Travel expectation of 25% to 50%

Accessibility Accommodation

If you are a qualified individual with a disability, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access site as a result of your disability. You can request a reasonable accommodation by sending an e-mail to or by calling 1.727.803.7515 with the nature of your request and contact information. Please do not direct any other general employment related questions to this e-mail or phone number. Please note that only those inquiries concerning a request for reasonable accommodation will be responded to from this e-mail address and/or phone number.

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