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QA Consultant Utilities

Life Sciences
Validation and Qualification
Bachelor, Master
Medior (3+)
Location
Puurs-Sint-Amands, Antwerp
Work type
Consultancy
Work model
Fulltime, On-site

Our client, a leading pharmaceutical manufacturer, is seeking a consultant to support their technical department with quality assurance documentation for critical utility systems. This role bridges the gap between technical operations and compliance by managing deviations, change controls, and root cause investigations.

Responsibilities

  • Own and manage the backlog of utility-related deviations and CAPA plans within established timelines.
  • Lead root cause analysis (RCA) sessions for recurring deviations involving HVAC, purified water, and environmental monitoring systems.
  • Author high-level quality documentation and deviation reports compliant with EU GMP Part I standards.
  • Support OOT/OOS trend analysis, risk stratification, and data integrity reviews for utility systems.
  • Provide technical oversight and serve as a backup for utility operations, including BMS alarm management and system monitoring.
  • Strengthen the link between preventive maintenance activities and deviation root causes to improve system reliability.

Requirements

  • You have a Bachelor or Master in Electromechanical, Mechanical, or Building Services Engineering.
  • You bring 3+ years of technical engineering experience within a GMP-regulated manufacturing environment.
  • You possess expertise in quality assurance processes including CAPA, deviation management, and root cause analysis (RCA).
  • You have hands-on technical knowledge of utility systems such as Purified Water (PW), HVAC/AHU, and BMS/EMS.
  • You're familiar with Commissioning, Qualification, and Validation (CQV) processes and EU GMP regulations.
  • You're comfortable with a documentation-heavy role and possess strong analytical troubleshooting skills.

Nice to Haves

  • Experience with FDA regulations and 21 CFR Part 11 data integrity standards.
  • Knowledge of validation engineering or maintenance management systems like SAP PM.
  • Prior experience in a lead or supervisory capacity within a technical or pharmaceutical environment.

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.
# 100953
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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