Onsite QC Team Lead – GMP & Lab Excellence

Takeda Pharmaceutical Co.; Wicklow; On-site; EUR 58,000 - 79,000; Full time

Job summary

Takeda Pharmaceutical Co. is seeking a QC Team Leader in Bray, Ireland, for a fully onsite role within the Quality Control Department.

You will ensure GLP/gCMP compliance, oversee a team of QC analysts and technicians, and drive continuous improvement with cGMP and regulatory expectations. The ideal candidate has a BSc in science and at least five years in an analytical lab with supervisory experience, plus GC and HPLC expertise.

Qualifications

• Minimum of a BSc in science or a related discipline.
• Minimum of 5 years' experience in an analytical lab with supervisory responsibilities.
• Technical experience with GC and HPLC analyses required.
• Experience implementing continuous improvement plans in QC environment.

Responsibilities

• Ensure QC lab compliance with GLP and cGMP.
• Lead and develop a team of QC analysts/technicians.
• Support production, QA, planning and shipping with timely, compliant service.

Skills

Team leadership

Performance management

Interpersonal communication

Problem solving

Organisational skills

Investigational writing

Self-starter

Safety awareness

Education

BSc in science

Tools

GC

HPLC

Job description

Takeda Pharmaceutical Co. is seeking a QC Team Leader in Bray, Ireland, for a fully onsite role within the Quality Control Department.

You will ensure GLP/gCMP compliance, oversee a team of QC analysts and technicians, and drive continuous improvement with cGMP and regulatory expectations. The ideal candidate has a BSc in science and at least five years in an analytical lab with supervisory experience, plus GC and HPLC expertise.