GMP Compliance Medior Pharmaceuticals F/M/X - Wavre

We are looking for an EHS Engineer with an experience in pharmaceuticals.You will own the end-to-end delivery of circa 30 risk analyses for warehouse and chemical-storage areas, ensuring full ADR, ergonomics and chemical-storage compliance across the site. · ...

We are looking for an EHS Engineer with an experience in pharmaceuticals. · Key Responsibilities · Risk Analysis & Field Work · – Conduct on-site inspections of warehouse zones, chemical-storage rooms and ADR areas.Draft and update activity sheets · Safety data sheets · ...

We are looking for an EHS Engineer with an experience in pharmaceuticals. · Risk Analysis & Field Work Conduct on-site inspections of warehouse zones, chemical-storage rooms and ADR areas. · Review existing analyses, identify gaps and produce clear, actionable risk-assessment rep ...

Amaris Consulting is looking for a QA Specialist to support a leading pharmaceutical client in managing quality oversight of Contract Manufacturing Organizations within the External Manufacturing – Drug Product team. · ...

We are looking for a skilled Commissioning and Qualification Specialist to join our dynamic team in the pharmaceuticals sector. · Lead the commissioning and qualification processes for HVAC systems and clean rooms. · ...

We are looking for a Project Manager with an expertise in CQV in the pharmaceutical sector. You will drive the roll-out of a new global Engineering Standard (ES) across 12 manufacturing buildings in Belgium. · ...

Amaris is looking for a QA Specialist to support a leading pharmaceutical client in managing quality oversight of Contract Manufacturing Organizations (CMOs) within the External Manufacturing – Drug Product (EM Q DP) team. · This role ensures product quality, · regulatory complia ...

We are looking for a Project Manager with an expertise in CQV in the pharmaceutical sector. · 4–6 years' experience in product & process engineering within pharma/biotech. · Proven project-management track record (planning, budgeting, risk, timeline). · ...

We are looking for a Project Manager Medior to be part of the cold chain department with the validation activities and digitalization initiatives for the pharmaceutical operations, · ...

We are looking for a skilled Commissioning and Qualification Specialist to join our dynamic team in the pharmaceuticals sector.The ideal candidate will have a minimum of 4 years of experience in the commissioning and qualification of critical equipment, including HVAC systems and ...

We are looking for a Project Manager with an expertise in CQV in the pharmaceutical sector.Key ResponsibilitiesCompare the new ES against existing Belgium SOPs and identify discrepancies. · Risk Assessment LeadershipPlan, facilitate and document risk assessments with local subjec ...

The candidate will support the implementation of automated systems within clinical laboratories by providing quality assurance oversight. They will ensure compliance with regulatory standards throughout the system lifecycle. · Ensure business processes, equipment, and automated/a ...

Amaris Consulting is an independent technology consulting firm providing guidance and solutions to businesses. · ...

We are looking for a Junior CSV Specialist to support the successful implementation of automated and computerized systems within clinical laboratories. · Bachelor's or Master's degree in Life Sciences, Engineering or related field. · ...

Job summary Lead quality assurance oversight for the implementation of automated and computerized systems within clinical laboratories and central scientific teams. Ensure compliance with global regulatory standards and internal quality systems to support pipeline delivery, audit ...

We are seeking a Quality Assurance Specialist to lead quality assurance oversight for the implementation of automated systems within clinical laboratories. The ideal candidate will have experience in computerized systems validation (CSV) and equipment qualification. · Lead QA ove ...

We are seeking a Junior QA Validation Computer Systems for our pharmaceutical and biotechnology clients in the Walloon Region. The successful candidate will be responsible for ensuring the quality of computerized systems and automation projects from design to validation and opera ...

Lead quality assurance oversight for the implementation of automated and computerized systems within clinical laboratories and central scientific teams. Ensure compliance with global regulatory standards and internal quality systems to support pipeline delivery, audit readiness, ...

Support the successful implementation of automated and computerized systems within clinical laboratories. · ...

We are offering international volunteer positions VIE for talented engineers and compliance specialists to support critical operations across our pharmaceutical sites in Belgium. · These roles are ideal for early-career professionals seeking hands-on experience in a regulated ind ...