COMPLIANCE ENGINEER (M/F/D), Akkodis

Solliciteren

Plaats

2440 Geel
België
België

Contract

Vooltijds, Onbepaalde duur

Datum gepubliceerd

2026-04-18

Online to:

2026-06-17
EUR 20.00 HOUR

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COMPLIANCE ENGINEER (M/F/D)

Akkodis
België
Andere
3 uren geleden

Who we are Akkodis 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. 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. Product & System Development, Validation & Verification, Manufacturing & Operations, Cloud Infrastructures & Security, Data Analytics & Artificial Intelligence, Digital & Software and Wireless & Connectivity. As Compliance Engineer, you will strengthen the Reliability and Support team within the Engineering & Maintenance department. You will focus on ensuring that engineering and maintenance activities are aligned with internal procedures and external requirements that apply to the pharmaceutical industry. You will work with the QMS system (VeeVa), analyze deviations across a wide range of technical systems, and support the implementation of corrective and preventive actions. The role requires frequent interaction with production, QA, and system owners, as well as a strong focus on quality upskilling and monitoring quality-related KPI within the E&M department. Take responsibility for drawing up actions in the QMS system (VeeVa) within the Engineering & Maintenance department and ensure timely follow-up of all related activities. Act as the central contact person in the Engineering & Maintenance department for performing analyses into the technical root cause of deviations across various technical systems. Perform structured investigations into deviations related to diverse systems, including process systems, HVAC, clean utilities such as WFI, ROW, and process gassenn, ensuring accurate documentation of findings. Support the drafting of any CAPAs, ensuring that corrective and preventive measures are clearly defined, technically sound, and aligned with quality and compliance requirements. Contribute actively to quality upskilling within the E&M department by sharing insights from deviation analyses and supporting continuous improvement of quality awareness. Good knowledge of legislation within the pharmaceutical industry, allowing correct interpretation and application of regulatory and compliance requirements in daily work. Experience with Quality Management Systems, ideally including practical use of systems such as the QMS system (VeeVa) in a technical or engineering environment. Background in a compliance-oriented role, providing familiarity with deviation handling, CAPAs, documentation standards, and quality audits in the pharmaceutical context. Ability to work effectively within the Reliability and Support team and the broader E&M department, collaborating on technical root cause analyses and quality upskilling initiatives. Stage 1: Initial telephone interview (15 min) with @Bo, Talent Acquisition Specialist.

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