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MSI Pharma recruits for jobs across the Life Sciences industry. We are strategically engaged with clients around the world and offer opportunities for temporary, interim and permanent roles.

Pharma jobs

Found 10 jobs
    • Europe
    • Competitive Salary
    • Posted 24 days ago

    ​Source Clinical IT SME (Fully Remote- work from anywhere in Europe) The team is responsible for managing and supporting various Veeva Vault systems used for clinical development and quality management at UCB.

    • Europe
    • Competitive Salary
    • Posted 24 days ago

    ​We are seeking a Consulting Project Manager to lead client implementation projects for technology solutions in the life sciences sector. This is a strategic, client-facing role requiring strong project management expertise, experience in regulated environments, and the ability to drive successful outcomes across global teams.

    • Belgium
    • Competitive Salary
    • Posted 24 days ago

    ​We are looking for a Procurement Project Manager to support a major construction project in Braine l’Alleud. You will manage procurement across various projects, focusing on construction, MEP, and process equipment. This global role requires close coordination with the procurement team and adherence to regulatory requirements.

    • Anderlecht
    • Competitive Salary
    • Posted 24 days ago

    Lead, Global Talent, Compensation & HRIS Tools (SuccessFactors Focus) ​Experience Required: 5-8 years of experience in HR processes, talent management, performance, and compensation cycles. Strong background in SuccessFactors with a focus on functional and business advisory aspects. Experience su...

    • Belgium
    • Competitive Salary
    • Posted 24 days ago

    ​We are seeking an experienced Procurement Manager based in Belgium to provide support for Building & Facilities procurement activities, including a major CAPEX project in the UK. The role requires independent work, strong knowledge of construction/facilities procurement, and experience in contract negotiation and vendor management. Immediate availability is essential, with potential for extension.

    • Belgium
    • Competitive Salary
    • Posted 24 days ago

    ​The IT Veeva Vault Quality Configuration Specialist will play a key role in managing, configuring, and improving the Veeva Vault Quality Suite (including Quality Docs and QMS) for a global pharmaceutical company. Based in Belgium with hybrid work flexibility. Ideal candidates will have experience in Veeva Vault, Quality Assurance, system administration, and Pharma IT compliance (CSV/GxP). Strong communication, adaptability, and technical skills are essential.

    • Belgium
    • Competitive Salary
    • Posted 24 days ago

    ​Join our international team as a Device Quality Lead, supporting the development and quality management of innovative medical devices like auto-injectors and pen injectors. This remote-friendly role (with some EU travel) is ideal for candidates experienced in ISO standards, supplier management, and risk control. Fluency in English is required; French is a plus. Help shape safer, smarter healthcare solutions — apply now!

    • Belgium
    • Competitive Salary
    • Posted 24 days ago

    ​UCB is hiring a Device Documentation Lead (remote, Belgium-based) to support regulatory documentation for a drug-device combination product. Perfect for detail-oriented professionals with a collaborative mindset.

    • Belgium
    • Competitive Salary
    • Posted 24 days ago

    ​We're seeking a CSV Expert with strong PCS 7 experience to support the qualification, validation, and remediation of computerized systems for a major biopharma building expansion project in Belgium. The role requires 8+ years of CSV experience, deep GMP knowledge, and strong collaboration skills. Primarily on-site with up to 60% remote flexibility.

    • Belgium
    • Competitive Salary
    • Posted 24 days ago

    Lead the selection and assessment of drug delivery devices for global clinical trials. Requires 8+ years’ experience, strong knowledge of medical devices and regulations (EU MDR, ISO13485), and a background in clinical trials. Work remotely from Belgium with a global, cross-functional team.

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