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Senior CSV and Data Integrity Engineer

Life Sciences
Validation and Qualification
Bachelor, Master
Senior (7+)
Location
Braine-l'Alleud, Walloon Brabant
Work type
Consultancy
Work model
Fulltime, Hybrid

Our client, a leading biotechnology organization, is seeking a Subject Matter Expert to lead commissioning and qualification activities for computer systems. This role focuses on ensuring that data integrity and validation standards are met for a major international capital expenditure project.

Responsibilities

  • Act as the subject matter expert and compliance lead for CSV and Data Integrity throughout the project lifecycle from design to reporting.
  • Drive the CSV portion of the project, ensuring all commissioning and qualification activities are completed in compliance with system requirements and project guidelines.
  • Execute Data Integrity Risk Assessments (DIRA) and perform comprehensive gap analyses for equipment and systems.
  • Oversee 21 CFR Part 11 compliance aspects, including audit trails, electronic signatures, system security, and access management.
  • Collaborate with IT and automation specialists to ensure correct implementation and testing of PLC, SCADA, and DCS systems.
  • Draft and coordinate the review of CSV technical documentation, including requirements, testing protocols, and summary reports.
  • Manage verification testing, lead deviation investigations, and resolve technical issues encountered during execution activities.

Requirements

  • You have a Bachelor or Master degree in Engineering or a related technical qualification.
  • You bring 5+ years of experience as a Lead or Subject Matter Expert in international CAPEX Commissioning and Qualification.
  • You possess extensive knowledge of CSV within the pharmaceutical or biotechnology industry, including risk-based approaches.
  • You have a deep understanding of GAMP-5, Annex 15, Eudralex, and ASTM E2500 standards.
  • You bring technical expertise in Data Integrity and process automation systems such as DCS, SCADA, and PLC.
  • You're a strong leader with the ability to make decisions under pressure and collaborate effectively with senior stakeholders.
  • You are fluent in English.

Nice to Haves

  • Experience with sterile, biotech, or single-use equipment.
  • Familiarity with electronic validation execution.

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.
# 101837
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Candidates must be legally authorised to work in the EU and possess the required language skills for the job location.
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