QC Technical Project Lead: Lab Systems & Compliance

Eisai Emea; Hatfield; On-site; GBP 65,000 - 90,000; Full time

Benefits offered by this job

Electric charging points for Electric/

Discretionary Bonus

Free onsite parking

Subsidised onsite restaurant and cafe

Learning and development opportunities

Retail discounts

Well-being & mental health awareness

Multi-faith prayer room

Job summary

Eisai EMEA is seeking a Quality Control Technical Project Manager to lead a team of specialists responsible for QC equipment and electronic systems (e.g., LIMS and CDS), and to drive qualification, validation, and change-control activities.

The role focuses on maintaining compliance with GMP, data integrity guidelines, and pharmacopeia requirements while delivering robust QC capabilities across manufacturing and testing processes.

Qualifications

• Degree or equivalent in a science discipline with GMP exposure.
• Strong knowledge of QC equipment and electronic systems qualification/validation.
• Experience managing QC equipment/electronic systems for 2+ years.
• Laboratory administration experience and end-user of QC systems.
• Excellent communication and people management skills.

Responsibilities

• Lead a team of technical specialists in QC lab projects.
• Oversee QC equipment and electronic systems, ensuring SOPs and GMP compliance.
• Develop and maintain a five-year equipment replacement plan.
• Manage New Product Introduction and Method Transfer.
• Lead QC compliance activities including data integrity and pharmacopeia reviews.
• Educate and train QC staff on equipment and software usage.

Skills

GMP knowledge

Data integrity understanding

Technical project management

QC equipment knowledge

Electronic systems qualification/val

Lab administration

Communication and people management

Education

Degree or equivalent in a science discipline

Tools

MS Office (Word, Excel, PowerPoint)

Job description

Eisai EMEA is seeking a Quality Control Technical Project Manager to lead a team of specialists responsible for QC equipment and electronic systems (e.g., LIMS and CDS), and to drive qualification, validation, and change-control activities.

The role focuses on maintaining compliance with GMP, data integrity guidelines, and pharmacopeia requirements while delivering robust QC capabilities across manufacturing and testing processes.