Analytical Laboratory Technical Leader
Hours : 37.5 hours per week. Monday – Friday, flexible working hours
Ref No:
HRJOB10304 Business Unit:
Pharma Services Location:
Loughborough, Leicestershire, UK Open To:
Internal and external candidates welcome to apply The Role The Analytical Laboratory Technical Leader will provide leadership and coaching for Senior Analysts, Analysts, and Technicians, enabling the delivery of complex projects. The post holder will act as the primary analytical lead for their assigned project. They will execute, delegate, and monitor the progress of work on a daily basis, ensuring project timelines are met. They will also be responsible for communicating progress to internal and external clients. As part of a busy team within a rapidly growing organisation, operating within a challenging industry, you will benefit from the numerous personal and professional developmental opportunities available throughout the Almac group. Candidate Criteria B.Sc. (or equivalent) in Chemistry or a Life Science based discipline Significant experience of analysing pharmaceutical drug products in a GMP environment Significant experience in: LC analysis Stability study design and testing HPLC method development Method validation Experience of supervising and managing cGMP laboratory activities and staff meeting demanding timelines Experience of leading analytical development activities in support of pharmaceutical development projects Experience of assessing and investigating quality events Experience of client interaction in a contract manufacturing company Closing Date:
Sunday 2nd February 2025 at 5pm local time
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HRJOB10304 Business Unit:
Pharma Services Location:
Loughborough, Leicestershire, UK Open To:
Internal and external candidates welcome to apply The Role The Analytical Laboratory Technical Leader will provide leadership and coaching for Senior Analysts, Analysts, and Technicians, enabling the delivery of complex projects. The post holder will act as the primary analytical lead for their assigned project. They will execute, delegate, and monitor the progress of work on a daily basis, ensuring project timelines are met. They will also be responsible for communicating progress to internal and external clients. As part of a busy team within a rapidly growing organisation, operating within a challenging industry, you will benefit from the numerous personal and professional developmental opportunities available throughout the Almac group. Candidate Criteria B.Sc. (or equivalent) in Chemistry or a Life Science based discipline Significant experience of analysing pharmaceutical drug products in a GMP environment Significant experience in: LC analysis Stability study design and testing HPLC method development Method validation Experience of supervising and managing cGMP laboratory activities and staff meeting demanding timelines Experience of leading analytical development activities in support of pharmaceutical development projects Experience of assessing and investigating quality events Experience of client interaction in a contract manufacturing company Closing Date:
Sunday 2nd February 2025 at 5pm local time
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