Analytical Method Transfer | Life Sciences

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Your role

As 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 transfers
• •Defining 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 standards
• •Authoring, reviewing, and approving analytical protocols, technical reports, and supporting documentation to ensure accuracy, compliance, and alignment with regulatory expectations
• •Reviewing and summarising data from analytical method transfers — including non-clinical statistical data evaluation — drawing clear, well-supported conclusions to drive decision-making
• •Coordinating laboratory readiness, tracking progress against timelines, and providing or facilitating technical troubleshooting and investigative support for any issues arising during the transfer process
• •Identifying and communicating potential risks to scope and timelines, proposing mitigation strategies, and providing regular updates to project teams and functional management

Your profile

• •You hold a degree in (Bio)Chemistry, Pharmaceutical Sciences, Biotechnology, or a related scientific discipline
• •You have a minimum of 2 years of experience in an analytical or quality control role within the pharmaceutical or biotech sector
• •You 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 standard
• •You 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 resolution

What you'll love about working here

• •Hybrid 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