CQV Engineer (H/F)

La mission

Efor is a leading consulting group specialized in Life Sciences, bringing together more than 3,200 consultants and experts and supporting over 1,000 clients worldwide, including 90% of the leading pharmaceutical, biotech and medtech companies. In Belgium, our teams contribute to high-impact industrial projects for major Life Sciences players such as UCB, GSK, Novo Nordisk, Takeda and Baxter, addressing key challenges across CQV, Quality, and Engineering. As part of our continued growth in Belgium, we are looking for CQV Engineers who want to bring their expertise to ambitious pharmaceutical and biotechnology projects, including new facilities, revamping, capacity expansion, new production equipment and optimization of existing installations. 🚀 Your role As a CQV Engineer, you will work at the heart of our clients’ investment projects, contributing to the successful commissioning and qualification of pharmaceutical facilities, systems and equipment in compliance with GMP requirements. Depending on your experience and area of expertise, you may be responsible for: • Defining and implementing Commissioning & Qualification strategies; • Preparing, reviewing and/or executing DQ, FAT, SAT, IQ, OQ and PQ activities; • Coordinating commissioning and qualification activities throughout the different project phases; • Reviewing qualification protocols, test results and raw data; • Identifying, investigating and following up on deviations through to resolution; • Preparing and/or approving qualification reports; • Ensuring compliance with GMP requirements throughout the project lifecycle; • Coordinating key stakeholders including Engineering, Quality, Production, suppliers and contractors; • Managing CQV activities in line with project milestones and timelines.