HRjob8639 - Analytical Group Leader - Loughborough, United Kingdom - Almac Group

Almac Group

Verified Company

Loughborough, United Kingdom

6 days ago

Posted by:

Tom O´Connor

beBee Recruiter

Description

Analytical Group Leader

Hours: 37.5 hours per week

Salary:
Competitive

Ref No:
HRJOB8642

Business Unit:
Pharma Services

Location:
Loughborough, Leicestershire

About The Role
To provide technical and managerial leadership to multiple large and small analytical teams. Primarily Raw Materials, Cleaning Verification, Environmental Monitoring, Laboratory Equipment and Laboratory Support

To manage the progress of Analytical work and ensure that project schedules are met and that the work is carried out safely, efficiently, compliantly, and accurately, providing regular updates to Analytical management.

To manage the Support Function of the Analytical Laboratories ensuring a high level of equipment availability, consumables availability and advising on future CAPEX programmes.

To actively support Pharma Services in delivering the Company's operational and business objectives.

About You
To be successful in this role, we're looking for you to have:

Significant experience of managing and leading analytical teams within a GMP/GLP laboratory supporting the development of pharmaceutical drug products. Including recruitment, performance management and talent management.
Supervision or Management of Pharmaceutical Raw material testing and or GMP Manufacturing Equipment Cleaning Verification, has gained a clear in depth knowledge of one of these.
History of responsibility for analytical instrumentation either hands on or leading an equipment team.
Gained a clear in depth knowledge of a wide range of analytical instrumentation and equipment.
A proven ability for solving and coaching others to solve analytical and laboratory based challenges.
Significant experience in the interpretation of data from a wide range of analytical techniques.
Experience of hosting aspects of laboratory quality audits and inspections by external bodies. This experience should have been gained from hosting aspects of many different cGMP/GLP quality audits.
Ability to work effectively on own initiative and effectively contribute within a team environment.
Managing and motivating analytical teams and delivering multiple projects within a concurrent timeframe.
Ability to build, maintain and inspire teams of people
Ability to present ideas and information clearly to multi disciplined teams
Excellent attention to detail.
Practical problem solving skills.
CChem MRSC or M.Sc./PhD (or equivalent) in Analytical Chemistry or Chemistry
Experience of Environmental Monitoring and microbiology applicable to pharmaceutical Oral Solid Dose Production.
Experience working with multiple stake holders to deliver successful outcomes to complex projects.
Experience running a team of Technicians supporting a busy analytical facility.
Experience of statistical data analysis techniques.
Experience of preparing or supporting the preparation of CMC regulatory submission documentation.
Experience of leading analytical development activities within a contract research environment.