Supervisor, Bioassay NPI

The Westport Bioassay department requires highly skilled personnel to fulfil several critical tasks. The Supervisor, Bioassay NPI is responsible for the oversight and operation of the Bioassay QC NPI laboratory. The group performs Cell-Based Potency Assay (CBPA) and ELISA testing of development and clinical products generated by Biologics Development Manufacturing and is responsible for release and stability testing following assay transfer and validation from PDS&T. This is for a fixed term contract of 12 months. 

The supervisor ensures that release and stability testing for products in the development pipeline is scheduled and completed in line with global request timelines, supporting uninterrupted clinical supply and the achievement of project milestones. The role also communicates results to key stakeholders, schedules ancillary laboratory activities—including critical reagent screening and qualification, laboratory housekeeping, paperwork review, and procedural updates—and supports personnel development, talent management, and succession planning within the team.

• Provide motivation to the team and take appropriate corrective action on individual or team performance where required through effective communication.
• Hold performance meetings in accordance with company policy.
• Take an active role in the recruitment of team members.
• Update Kronos and take appropriate action where an individual’s attendance or timekeeping is below the expected standard.
• Actively participate in the training and certification of new employees.
• Ensure all activities are completed in line with regulatory requirements, including QA and EHS requirements, and corporate standards.
• Maintain capacity in line with business needs, including recruiting staff and managing constraints appropriately.
• Coach and develop Analytical Technology Specialists to support succession planning and Individual Development Plans (IDPs).
• Provide required data in line with testing timelines to support product release and the global stability programme.
• Provide team KPI data.
• Attend departmental and OPEX meetings.
• Review and approve local and corporate documents.
• Work directly with Microbiology, Chemistry, Production, QA, and Planning to ensure the timely release of development products.
• Ensure the timely review of data generated within the team.