Analytical Group Manager

TERUMO BCT, INC; Millbrook; On-site; GBP 60,000 - 85,000; Full time

Job summary

Terumo BCT in Larne, Northern Ireland, is seeking an Analytical Group Manager to lead multiple analytical teams, ensuring high scientific and quality standards in chemistry testing and method development.

You will own QA documentation, drive CAPA closures, oversee method transfers, and align laboratory performance with site and company goals. The role requires extensive lab experience and strong leadership across functions.

Qualifications

• Degree in Chemistry or closely related subject.
• Extensive hands-on laboratory operations experience.
• Experience in staff management.
• Knowledge of EP/USP methods.
• Experience with laboratory equipment: AA, HPLC, GC, IC, ICP.

Responsibilities

• Mentor analysts and managers; uphold scientific rigor and documentation.
• Ensure all work conforms to approved methods and QMS.
• Ensure regulatory compliance of analytical results and reports.
• Provide technical review of laboratory data and investigations (NC, OOS, OOT).
• Lead development, validation/verification and optimization of analytical methods per ICH guidelines.
• Support product development and lifecycle management with stability-indicating methods.
• Oversee method transfers between departments or sites.
• Maintain compliance with cGMP, GLP and internal standards.
• Own SOPs, method protocols, and instrument calibration.
• Implement CAPAs and ensure timely closure.

Skills

Multitasking

Communication & collaboration

Education

Chemistry degree

Tools

AA

HPLC

GC

IC

ICP

Job description

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Analytical Group Manager

Date: Oct 22, 2026

Analytical Group Manager

(26_36)

Terumo BCT is a Global leader in blood management, blood safety, therapeutic apheresis, cell therapy and cell collections. We have an exciting opportunity for an Analytical Group Manager to join Terumo BCT- Larne.

The Analytical Group Manager will provide management, leadership and coaching to multiple operational analytical teams, servingas the technical leader and subject matter expert for chemistry and ensuring that analytical testing, method development and regulatory compliance meet the highest scientific and quality standards. In addition, the post holder will have responsibility for strategic oversight to ensure safe, efficient and compliant lab operations.

General Duties

• Mentor analysts, senior analysts and department managers; uphold a culture of scientific rigor and good documentation practices
• Ensure all analytical and laboratory work is conducted in conformance with approved methods and systems to ensure adherence to the site QMS
• Ensure accuracy, traceability, and regulatory compliance of all analytical results and reports
• Provide technical review and approval of laboratory data and investigations (e.g., NC, OOS, OOT).
• Lead the development, validation / verification and optimization of analytical methods per ICH and pharmacopeial guidelines.
• Support product development and lifecycle management with stability-indicating methods and formulation analysis
• Manage feasibility testing of new methods
• Manage method transfers between departments (AD/QC) or sites (CMOs), ensuring readiness and robustness
• Maintain and enforce compliance with cGMP, GLP and internal quality standards
• Own and oversee SOPs, analytical method protocols, laboratory documentation, training records and instrument calibration and qualification programs.
• Implement CAPAs and ensure closure in alignment with regulatory and internal expectations
• Act as a key participant or host during internal audits, customer audits, regulatory inspections and quality reviews
• Define, track, and report KPIs (e.g., on time release, first-pass yield, training compliance, NC/CAPA closure rates)
• Use data-driven insights to improve lab efficiency, reduce errors and drive continuous improvement initiatives
• Collaborate with site leadership to align laboratory performance with broader organizational goals
• Champion laboratory safety practices in compliance with EH&S regulations and expectations
• Act as a cross-functional liaison with manufacturing, regulatory and external partners
• Contribute to departmental strategy, budgeting and technology planning
• Liaise with Global TBCT sites to advise on analytical related issues.
• Own QC laboratory throughput and testing prioritisation processes to ensure analytical activities are aligned with production schedules, customer commitments and inventory requirements
• Provide strategic leadership for batch release testing, ensuring timely generation, review and approval of analytical results to support on‑time product disposition and release.
• Partner closely with Manufacturing, Quality Assurance, Supply Chain and R&D teams to balance analytical turnaround times, compliance requirements and operational priorities, minimising production delays while maintaining data integrity and quality standards.
• Establish and monitor laboratory performance metrics relating to testing cycle times, sample backlog, testing right-first-time, and release performance, driving continuous improvement to improve responsiveness and efficiency.
• Lead the analytical support for in‑process manufacturing testing, ensuring rapid, scientifically sound interpretation of results to enable timely operational decision making and process control.
• Ensure appropriate laboratory resource planning, staffing and capability to meet fluctuating manufacturing demands, critical release timelines and business continuity requirements.
• Act as the primary escalation point for critical production‑related analytical issues, providing risk‑based recommendations and expediting investigations to minimise manufacturing disruption.
• Drive continuous improvement initiatives focused on reducing analytical turnaround times, optimising workflow efficiency and increasing laboratory capacity without compromising compliance or data quality.
• Implementation and maintenance of LIMS (laboratory information management system) across laboratories.

Education

• A degree in Chemistry or closely related subject

Experience

• Extensive hands‑on experience in laboratory operations, demonstrating a high level of technical competence and scientific understanding
• Experience in the Management of staff
• Knowledge of current EP/USP methods
• Experience in use of laboratory equipment - AA, HPLC, GC IC, ICP

Skills

• Ability to manage multiple priorities and work collaboratively across departments
• Excellent organisational, communication, and problem‑solving skills

Additional Information

• Occasional travel to global TBCT locations

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