Qualification‑Validation Engineer (Pharma)Walloon Brabant, BelgiumJoin Nalys and contribute to impactful engineering projects in the pharmaceutical industry!At Nalys, we are passionate about engineering, life sciences, and the people who drive these industries forward. As a fast‑growing consultancy supporting leading pharmaceutical organizations, we offer our consultants the opportunity to grow, innovate, and make meaningful impact.We are looking for a motivated Qualification‑Validation Engineer to support one of our long‑standing partners located near Brussels. In this role, you will play a key part in ensuring that equipment, systems, and processes meet the highest standards of compliance and performance within a regulated environment.IntroductionAs a Qualification‑Validation Engineer, you will be involved in the qualification and validation of laboratory and production equipment, utilities, and related systems. Working closely with multidisciplinary teams, you will help define validation strategies, prepare documentation, supervise execution, and support continuous improvement activities. This position offers a dynamic environment, strong technical exposure, and the chance to grow within complex pharmaceutical projects.Key ResponsibilitiesParticipate in the planning, execution, and review of qualification and validation activities (IQ/OQ/PQ)Draft and update validation documents such as URS, validation plans, test protocols, reports, and risk assessmentsAct as a point of contact for validation topics across functions (engineering, QA, QC, maintenance, production)Support commissioning activities for new or upgraded equipment and systemsEnsure compliance with GMP standards, internal procedures, and industry guidelinesContribute to deviation, CAPA, and change control processes related to validation scopeMaintain accurate documentation and ensure proper archiving of validation filesSuggest improvements to enhance validation processes and operational efficiency.RequirementsYou hold a Master’s or Bachelor’s degree in Engineering, Life Sciences, Industrial Sciences, or a related fieldYou have a first experience (or strong internship background) in equipment qualification, validation, or quality/compliance within a pharmaceutical or biotech environmentYou have a good understanding of GMP, validation principles, and regulatory expectationsWith a strong analytical mindset, structured working style, and ability to prioritizeAnd an excellent communication and teamwork abilitiesYou are fluent in English; knowledge of French or Dutch is a plus.Recruitment Process at NalysOur recruitment journey is designed to be smooth, transparent, and respectful of your time:Introductory call with our Talent Acquisition Specialist, to answer all of your HR questions and assess your expectationsTechnical discussion with one of our Technical Referents to a deeper technical talkA Last meeting with our Director Life Sciences BU, Jimmy Rousseaux.How to ApplyFeel inspired to join an innovative engineering community?Send your CV to directly on linkedin or apply directly via our careers platform.Our team will get in touch shortly to discuss your ambitions and how they align with our opportunities.