Analytical Method Transfer | Life Sciences

Capgemini Engineering

Diegem

Ibrido

EUR 65.000 - 90.000

Tempo pieno

4 giorni fa
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Vantaggi offerti da questo lavoro

Hybrid work
GetCelebrating recognition programme
FlexAbroad – 45 days abroad

Descrizione del lavoro

Capgemini Belgium is seeking an Analytical Method Transfer Consultant specializing in biologics to join a hybrid team. Based in Beerse or Brussels with remote flexibility, you will coordinate method transfers, define transfer strategies, and author protocols and reports to ensure GMP-compliant transfer of analytical methods for biologics.

You will collaborate with cross-functional teams, manage timelines, anticipate risks, and support lab readiness across sites.

Competenze

  • Minimum 2 years in analytical or quality control within pharma/biotech.
  • Hands-on analytical techniques with GMP awareness.
  • Experience authoring protocols and reports to a high standard.

Mansioni

  • Coordinate analytical method transfers across laboratories and define scope and timelines.
  • Develop transfer strategies, select samples, acceptance criteria, and statistics.
  • Author, review and approve protocols and reports ensuring GMP compliance.
  • Track progress, manage risks, and support lab readiness across sites.

Conoscenze

HPLC
GMP compliance
Analytical method transfer
Cross-functional collaboration

Formazione

Degree in Chemistry/Biochemistry or related field

Descrizione del lavoro

Choosing Capgemini means choosing a company where you will be empowered to shape your career in the way you’d like, where you’ll be supported and inspired by a collaborative community of colleagues around the world, and where you’ll be able to reimagine what’s possible. Join us and help the world’s leading organizations unlock the value of technology and build a more sustainable, more inclusive world.Your roleAs an Analytical Method Transfer Consultant specialising in biologics, you will be embedded within a leading pharmaceutical environment, playing a central role in ensuring the successful transfer of analytical methods across laboratories. Working in a hybrid setup, on-site in Beerse and Brussels with remote flexibility, you will collaborate with diverse stakeholders and bring both technical depth and project leadership to every engagement. In this role you will play a key role in:Collaborating with cross-functional teams including method and specification owners, internal QC and stability laboratories, regulatory affairs, and external quality partners to define the scope, timelines, and country-specific requirements for analytical method transfersDefining and documenting analytical method transfer strategies for biologics (large molecules), including identification of appropriate samples, acceptance criteria, and statistical evaluation approaches, building robust transfer plans in line with GMP standardsAuthoring, reviewing, and approving analytical protocols, technical reports, and supporting documentation to ensure accuracy, compliance, and alignment with regulatory expectationsReviewing and summarising data from analytical method transfers — including non-clinical statistical data evaluation — drawing clear, well-supported conclusions to drive decision-makingCoordinating laboratory readiness, tracking progress against timelines, and providing or facilitating technical troubleshooting and investigative support for any issues arising during the transfer processIdentifying and communicating potential risks to scope and timelines, proposing mitigation strategies, and providing regular updates to project teams and functional managementYour profileYou hold a degree in (Bio)Chemistry, Pharmaceutical Sciences, Biotechnology, or a related scientific disciplineYou have a minimum of 2 years of experience in an analytical or quality control role within the pharmaceutical or biotech sectorYou have hands-on experience with analytical techniques such as HPLC, and a solid understanding of GMP requirements, method validation principles, and quality control processes for biologics (large molecules)You are experienced in managing or coordinating analytical method transfers, with the ability to author and review technical documents such as protocols and reports to a high standardYou communicate with confidence across multidisciplinary teams, are comfortable managing competing priorities in a project environment, and bring a proactive, structured approach to identifying risks and driving timely resolutionWhat you'll love about working hereHybrid working – We encourage flexibility when it comes to when and where work gets done. Employees work with their managers to determine an arrangement that works best for their role and personal circumstances.GetCELEBRATING – Our Employee Recognition Program is here to enable us to recognize inspiring people like you. The program appreciates both big and small wins, as well as the everyday efforts that help us all achieve the future we want. GetCelebrating makes the day-to-day feedback and kudos received from colleagues, exchangeable for prizes and gifts.FlexAbroad – Employees in 20+ countries can work abroad for up to 45 days in a 12-month period.Capgemini is an AI-powered global business and technology transformation partner, delivering tangible business value. We imagine the future of organizations and make it real with AI, technology and people. With our strong heritage of nearly 60 years, we are a responsible and diverse group of 420,000 team members in more than 50 countries. We deliver end-to-end services and solutions with our deep industry expertise and strong partner ecosystem, leveraging our capabilities across strategy, technology, design, engineering and business operations. The Group reported 2024 global revenues of €22.1 billion.Make it real | www.capgemini.com
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