Amaris Consulting - Belgium

Join a Brussels-based team as a Junior Power Platform & SharePoint Developer. Leverage your 1-3 years of experience with Power Apps, Power Automate, and SharePoint to maintain and enhance business applications. Fluency in English, French, and Dutch is mandatory. Benefit from a multicultural envir...

Join a dynamic team in Brussels as a Software Developer under the V.I.E programme, driving digital transformation in the life sciences sector. You’ll design and maintain applications for manufacturing and regulated processes using Python, Java, or C. Ideal for candidates with 3+ years of experien...

Business Manager role in Belgium: drive growth in a fast-paced, international environment. Identify prospects, manage key accounts, and recruit top talent. Requires a Master’s in business/engineering, fluency in Dutch, French & English, and a competitive mindset. Enjoy a dynamic culture, robust t...

Seeking a **Deviation Maintenance Pharma** specialist in **Brussels, Belgium** to ensure GxP compliance for a Life Sciences client. You will own routine QA activities, manage deviations and CAPAs, and perform a targeted gap-assessment of procedures. Requires proven GxP QA experience, fluency in *...

Join Amaris Consulting as a Supply Chain & Logistics Specialist in Brussels. You will manage inventory, optimize supplier performance, and handle import/export logistics using ERP systems. The role requires fluency in French, Dutch, and English, plus 3-6 years of experience. Benefit from a divers...

Lead the technical evolution of LIMS (LabWare) in a major European QC lab transformation. Apply your GxP expertise to design compliant solutions and support deployments in Braine-L'alleud. This role combines deep technical leadership with strategic impact in the pharmaceutical sector.

Lead GMP QA operations for clinical trial materials and companion diagnostics in Mechelen. You will build and mentor a team, ensure EU/FDA compliance, and oversee batch release. Requires 7+ years' GMP QA experience in pharma/medical devices, team leadership, and fluency in English and Dutch. Join...

Join our client's Site Validation team in Belgium as a Qualification & Validation Engineer. Execute GMP protocols for equipment and process parameters in a biological drug-substance environment. Requires 4-6 years' pharma QV experience and fluency in French & English. Benefit from rapid growth an...

Join our team in Wavre as an SAP Quality Control Specialist. You will configure and maintain SAP QC inspection plans, supporting AGV system integration and managing ECO/ECR workflows. This administrative role requires 4-6 years of hands-on SAP QC experience and exceptional data accuracy. Enjoy an...

Join our GMP analytical team in Beerse as an Associate Scientist. Develop and validate Karl Fischer titration and HPLC/UPLC methods for pharmaceutical testing. Ensure compliance with strict regulatory standards in a dynamic, international environment. Grow your career with prestigious projects in...