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Validation Consultant - CSV & IT Quality

Life Sciences
Validation and Qualification
Bachelor
Advanced (5+)
Location
Ghent, East Flanders
Work type
Consultancy
Work model
Fulltime, Hybrid

Our client, a global biotechnology organization, is seeking a professional to support their digital technology compliance team with computer systems lifecycle management and IT quality processes. The role involves ensuring the integrity and compliance of computerized systems within a highly regulated environment.

Responsibilities

  • Write, review, and approve validation and qualification deliverables within the electronic document management system.
  • Ensure compliance with internal SOPs and external regulations including GxP, SOx, and Data Privacy.
  • Deliver project validation and qualification requirements consistently and within specified timelines.
  • Assist in the development and review of validation and qualification SOPs and templates.
  • Resolve computerized system validation compliance issues and manage quality events such as CAPAs, deviations, and change controls.
  • Maintain effective and open communication with stakeholders across quality, data engineering, and security domains.

Requirements

  • You have a Master or Bachelor in Computer Science, Life Sciences, or Engineering.
  • You bring 8+ years of experience as a Validation Consultant or Quality Manager for computer systems within the pharmaceutical or biotech industry.
  • You possess expert knowledge of regulatory standards such as FDA 21 CFR Part 11, EU Annex 11, GAMP5, and CSA.
  • You have extensive experience with the qualification of infrastructure and cloud platforms such as Azure, AWS, or OCI.
  • You bring hands-on experience with cloud data warehouses like Snowflake or Databricks, data visualization tools such as Tableau or Power BI, and AI governance for LLMs.
  • You’re a proactive communicator with a critical mind, high attention to detail, and a pragmatic approach to problem-solving.
  • You are fluent in English.

Nice to Haves

  • Experience with Veeva, ERP, QMS, ServiceNow, or Jira.
  • Proficiency with the latest versions of the MS Office software package.

Offer

  • Enjoy a competitive salary package with extra perks that recognize your talent.
  • Advance your career with a clear growth path, coaching, and mentoring to support you.
  • Thrive in a dynamic and supportive environment where you can truly make an impact.
  • Work when and where you perform best, ensuring an optimal work-life balance.
  • Choose a flexible transport solution, from a company car to a public transport subscription.
  • Expand your network and enjoy unforgettable moments at exclusive events and afterworks.
  • Grow your skills with external courses and our in-house Pauwels Academy.
  • Work on exciting projects with industry leaders in Life Sciences, Engineering & Digital.
  • Seize opportunities at every level, from a strong start to career acceleration and expert collaboration.
# 101863
With a plus sign and country code (e.g. +32 400 00 00 00).
We accept Word and PDF files up to 3 MB.
Candidates must be legally authorised to work in the EU and possess the required language skills for the job location.
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