Project Manager Digitalization Pharmaceuticals F/M/X - Wavre

Job Description · Key Responsibilities · Validation Strategy & Documentation · Ensure a comprehensive and compliant validation lifecycle, including: · Development, review, and approval of validation documentation: · Validation Plan (VP) · IOQ/PQ validation protocols (equipment an ...

Job Description · Key Responsibilities · Validation Strategy & Documentation · Ensure a comprehensive and compliant validation lifecycle, including: · Development, review, and approval of validation documentation: · Validation Plan (VP) · IOQ/PQ validation protocols (equipment ...

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 ...

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 ...

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 ...

Job Description · Mission Overview · Lead the digital transformation of manufacturing operations, driving strategic digital initiatives that enhance operational excellence, regulatory compliance, and competitive advantage in vaccine production. · Key Responsibilities · Strategic ...

Amaris Consulting is seeking a Digital Project Leader for Pharmaceuticals in Wavre, Walloon Region. The candidate will lead the replacement of SAP ECC cold-chain tracking with Parkour's TOST platform. · Gap Analysis: Map Belgium site processes against global TOST template. · Vali ...

We are looking for a Project Manager with expertise in CQV in the pharmaceutical sector to drive the roll-out of a new global Engineering Standard (ES) across manufacturing buildings. · Gap Analysis: Compare the new ES against existing Belgium SOPs and identify discrepancies. · R ...

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 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 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. · ...

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). · ...

+ Job summary: Amaris is looking for a QA Specialist to support a leading pharmaceutical client in managing quality oversight of Contract Manufacturing Organizations (CMOs). · + Qualifications: University degree in a scientific field; 4–6 years of experience in cGMP-regulated env ...

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 ...

Lead the replacement of SAP ECC cold-chain tracking with Parkour's TOST platform across Belgium operations as a critical S/4HANA readiness step. · ...

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 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 ...