As a CSV Consultant, you'll contribute to the validation of computerized systems in regulated Life Sciences environments. You'll ensure that digital solutions meet compliance standards and support quality, safety, and data integrity across pharma, biotech, and medtech organizatio ...

Join us in driving progress in the working world and beyond. Plan and coordinate IT quality/computer system validation (CSV) projects and/or IT audits, provide regulatory compliance, IT quality and computer validation guidance and support, create validation deliverables, perform ...

ALTEN Belgium is a leading consultancy company in the fields of Engineering, Life Sciences and IT in which our people and clients are central. · Act as Process Owner for local computer systems validation management. · Maintain current Validation Master Plans; oversee timely execu ...

We are currently looking for a CSV Engineer to start on a project at one of our clients within the pharmaceutical industry in Flanders. · Act as Process Owner for local computer systems validation management. · Maintain current Validation Master Plans; oversee timely execution. · ...

Are you passionate about both science and IT? · Do you want to contribute to cutting-edge projects in the Life Sciences while specializing in Computer Software Validation (CSV)? · Manage and oversee project deliverables for cutting-edge applications · Provide full-cycle support t ...

Join our expanding Software and Services division at QbD as a CSV Specialist. Contribute to cutting-edge projects in the Life Sciences while specializing in Computer Software Validation (CSV). · Manage and oversee project deliverables for cutting-edge applications. · Provide full ...

Wij zijn op zoek naar een Compliance Engineer – Automation & CSV voor een farmaceutisch bedrijf in Beerse. · Master of bachelor in een technische richting · Minstens 3 à 5 jaar ervaring in een GMP-omgeving · Kennis van relevante regelgeving en richtlijnen · Ervaring met één of me ...

Farma Consulting & Partners zoekt een getalenteerde en gemotiveerde collega voor project ondersteuning. We zoeken naar technische vaardigheden, maar ook een positief mindset en de juiste soft skills. · Min. 2 jaar ervaring binnen QA, Validatie of CSV · Consultant in een dynamisch ...

We are looking for a CSV Specialist – Medior to strengthen our quality and compliance team. This role offers the opportunity to contribute to high-value projects while benefiting from Nalys' collaborative culture and support. · Lead validation projects including process equipment ...

We are currently looking for a CSV & DI Team Leader at one of our clients. · Provide direction on CSV & DI best practices and corresponding science-based risk management approaches · Oversee the various projects and corresponding resources (contractors), applying diligent project ...

CONSULTYS BENELUX is op zoek naar een Life Science Consultant om het consultancyteam te versterken en bij te dragen aan de groei in Vlaanderen. · Masterdiploma in life sciences, biotechnologie, farmaceutica of bio-ingenieurswetenschappen · Ervaring in een GMP-omgeving · Goed inzi ...

MindCapture is looking for a Validation Engineer to take GMP critical systems to the next level. Challenging projects at an international healthcare leader, a competitive salary package with full benefits, and plenty of room to grow your career. · Validation execution: Develop, i ...

At Amaris Consulting, you will join an international and dynamic environment where you can develop your career within a fast-growing organization. Our values – entrepreneurship, trust, autonomy, continuous learning, and diversity – are at the heart of everything we do. We believe ...

Join an international and dynamic environment where you can develop your career within a fast-growing organization. Our values – entrepreneurship, trust, autonomy, continuous learning, and diversity – are at the heart of everything we do. · Support the QA Engineering department i ...

Ben jij een ervaren validatie-expert met een passie voor geautomatiseerde systemen en softwarepakketten? · Minimaal 3 jaar ervaring in de farmaceutische sector en een GMP-omgeving. · Ervaring met CSV. · Sterke communicatieve vaardigheden. · Selfstandig en leergierig, met het verm ...

Ben jij een ervaren validatie-expert met een passie voor geautomatiseerde systemen en softwarepakketten? Voor onze klant in Geel zijn we op zoek naar een Validatie Ingenieur die ervoor zorgt dat onze processen en systemen te allen tijde voldoen aan de hoogste kwaliteits- en compl ...

Avertim is a uniquely positioned management consulting group that bridges the gap between strategy, technology, and operations. Founded in 2007 and headquartered on Brussels' iconic Avenue Louise, Avertim has grown into a European consultancy with over 350 consultants across Belg ...

As a MES Project Manager, you will lead Manufacturing Execution System implementation and optimization projects within regulated Life Sciences environments. · Lead end-to-end MES implementation projects, from scoping and design to deployment and validation · Manage project timeli ...

As a MES Project Manager, you will lead Manufacturing Execution System implementation and optimization projects within regulated Life Sciences environments. · Lead end-to-end MES implementation projects, from scoping and design to deployment and validation · Manage project timeli ...

As a MES Project Manager, you will lead Manufacturing Execution System implementation and optimization projects within regulated Life Sciences environments. · Lead end-to-end MES implementation projects, from scoping and design to deployment and validation · Manage project timeli ...

Join Nalys, a fast-growing consultancy company specialized in high-tech engineering and life sciences, as a QA Validation Specialist. You will play a critical role in ensuring the compliance and robustness of validation activities across various departments. · QA validation for e ...