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Responsibilities
Who we areAkkodis is a global digital engineering and smart industry leader, bringing together talent and technology to engineer a smarter future. With more than 50,000 experts worldwide and over 1,000 in Belgium, we support companies across industries in innovation, digital transformation and R&D; from consulting and talent solutions to end-to-end project delivery. Driven by passion, expertise and impact, we make incredible happen.In Belgium, we operate through 7 dedicated practices, where our consultants receive the technical guidance, coaching and support they need to grow and fully unlock their potential. We believe in empowering our talent by providing the right expertise, knowledge-sharing and development opportunities to help them thrive. Our practices: Product & System Development, Validation & Verification, Manufacturing & Operations, Cloud Infrastructures & Security, Data Analytics & Artificial Intelligence, Digital & Software and Wireless & Connectivity.Akkodis is part of the Adecco Group.MissionAs Commissioning & Qualification (C&Q) Subject Matter Expert (SME), you will oversee and mentor a team of seven professionals. You will be the primary contact for equipment qualification, requalification, and improvement projects within a GMP environment. Your role involves ensuring that critical production facilities and sterile equipment consistently comply with quality standards. Combining technical expertise with people management, stakeholder management, and a hands-on approach, you will swiftly address urgent issues and actively contribute to CAPAs, non-conformances, and quality improvementsYour responsibilitiesCoordinate and execute (re)qualifications using V-model and risk-based approachInitiate and follow up on improvement projects with short turnaround timesPrepare, review, and approve validation documentation and technical reportsSupport audits and inspections to ensure compliance with GMP guidelinesActively participate in meetings, bridging operations, quality, and engineeringManage CAPAs and follow up on non-conformances to improve quality standardsEnsure systems and processes remain compliant with GMP guidelines and internal standardsWhat skills do you bring to the table?Master's degree in bioengineering, chemistry, pharmacy, or equivalent fieldMin of 5 years of experience in equipment qualification, validation, or quality in a GMP environmentStrong technical knowledge of sterile equipment and validation processesProficient in CAPAs and quality improvement projectsExperience in people management or a strong ambition to grow in this areaFluent communicator in both Dutch and English languagesSocial, flexible, and able to quickly integrate into a dynamic teamOur recruitment processStage 1: Initial telephone interview (15 min) with @Bo, Talent Acquisition Specialist.Step 2: Interview (60 min) with a Business Manager.Step 3: Interview (60 min) with the client.
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