Senior Quality Engineer (Pharma)

TL;DR

Senior Quality Engineer (Pharma): Preventing deviations and improving compliance in a cGMP environment with an accent on deviation and CAPA management. Focus on driving effective preventive and corrective actions, managing change, and ensuring product safety.

Location: Belgium (implied by company growth and Dutch Pharma context)

Company

An independent technology consulting firm providing guidance and solutions across Information Systems, Telecom, Life Sciences, and Engineering.

What you will do

• Analyze quality deviations to identify root causes, clusters, and trends.
• Lead deviation and CAPA management to ensure robust investigations and preventive measures.
• Collaborate with topic leaders to define and implement process improvements and change management.
• Monitor action plans and use data analysis to track residual risks and performance indicators.
• Ensure strict compliance with cGMP standards across production facilities and documentation.
• Support Operational Excellence and transformation initiatives related to quality.

Requirements

• 7–10 years of experience in a GMP environment (QA, QC, or Manufacturing).
• Proven expertise in deviation and CAPA management.
• Dutch fluency is mandatory.
• Experience in Operational Excellence and Transformation Management.
• Strong analytical mindset and professional data analysis skills.
• Ability to work in a cross-functional, regulated international environment.

Culture & Benefits

• Opportunities for rapid career growth within a fast-expanding Belgian office.
• Exposure to prestigious projects in the pharmaceutical and biotechnology sectors.
• Agile and dynamic international work environment promoting meritocracy and intrapreneurship.
• Commitment to diversity and an inclusive workplace for all qualified candidates.

Hiring process

• Brief virtual or phone introductory call to discuss motivations.
• Average of three interviews with line managers and team members.
• Potential case study or technical assessment depending on the specific requirements.