Amaris Consulting

Join a major bio-manufacturing digitalization program in Braine-L'alleud. As an MES & OSIsoft PI Consultant, you will own process packages from requirements to qualification in a GxP environment. Requires 4-6 years in pharma/biotech, hands-on MES (e.g., PAS-X) and PI expertise, plus fluent Englis...

Join our global team in Singapore as a QC Microbiologist. You will perform critical biological testing, environmental monitoring, and support GMP-compliant lab operations. The role requires a life sciences background, meticulous attention to detail, and experience with lab equipment and documenta...

Join Johnson & Johnson's MSAT team in Beerse as a Lifecycle Management Consultant. You will manage change controls for primary packaging materials in large molecule drug manufacturing. The role requires 4-6 years of pharma experience, GMP knowledge, and skills in change management systems. This i...

Join Amaris as a QA Specialist in Wavre, ensuring GMP compliance for a leading pharmaceutical client. You will manage quality oversight of CMOs, handling batch release, deviations, and change control. This role requires 4-6 years of cGMP experience, fluency in French/English, and expertise in SAP...

Join our Operational Quality team in Wavre as a GMP Compliance Medior. You will strengthen QA oversight and Environmental Monitoring across three GMP production buildings. The role involves designing harmonized tools, leading inspection rounds, and authoring key documentation. We seek a Life Scie...

Join our international team in Singapore as a Quality Operations Associate. You will ensure compliance by reviewing and approving electronic batch records within the pharmaceutical industry. This role requires a relevant degree, strong attention to detail, and experience with electronic record sy...