QA Qualification Engineer

• Review and approve qualification documents including SOPs, user requirements, and risk analyses to maintain regulatory compliance.
• Review quality records such as test plans, test scripts, Change Controls, and CAPAs.
• Participate in engineering teams to provide cGMP guidance for the introduction of new or upgraded systems and processes.
• Manage and follow up on deviations occurring during the execution of qualification activities.
• Communicate status updates regarding quality, compliance, and planning to the broader quality assurance team.

• You possess a background in the chemical or pharmaceutical industry with specific experience in equipment qualification.
• You bring sound knowledge of cGMP regulations and guidelines.
• You have experience with manufacturing systems and document management tools such as TruVault.
• You have worked with problem reporting and change request systems such as Trackwise or Comet.
• You are able to translate technical information for various organizational levels and manage multiple projects simultaneously.
• You are fluent in English and Dutch.

Nice to Haves

• Experience with digital test tools such as Kneat.

• 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.