Mary Bolt is recruiting for an excellent opportunity for a QC Supervisor to work within the Pharmaceutical Analytical division of a global contract development and manufacturing organisation, and provide technical and operational leadership, training and coaching to the analytical team. This role will be based in Leicestershire on a permanent basis.
Job Summary:
To manage the progress of Analytical work to GMP requirements and ensure that project schedules are met and that the work is carried out efficiently and accurately.
Responsibilities include:
-Taking full ownership for the analytical activities required as part of their assigned projects.
-Actively managing the performance of Technical Leaders, Senior Analysts, Analysts and Technicians assigned as their direct and indirect reports.
-Preparing, reviewing and approving any protocols.
-Ensuring laboratory cGMP procedures/systems are adhered to and investigate and manage any non-compliance issues.
On offer is a competitive salary plus excellent benefits (pension, healthcare, flexible working, childcare vouchers, free parking, health promotions, death in service benefits and more).
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Qualifications, Skills and Experiences:
-BSc (or equivalent) in Chemistry or a Life Science subject with a significant chemistry portion.
-Significant experience of leading analytical activities for Pharmaceutical drug products in a cGMP environment.
-Significant experience of Analytical method development, this must include a high level of HPLC, Analytical Validation, this must include a high level of HPLC and Stability study design and testing.
-A good understanding of the pharmaceutical drug development process from an analytical perspective.
Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained.
CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 47001 in all correspondence.
INDGEN
Job Summary:
To manage the progress of Analytical work to GMP requirements and ensure that project schedules are met and that the work is carried out efficiently and accurately.
Responsibilities include:
-Taking full ownership for the analytical activities required as part of their assigned projects.
-Actively managing the performance of Technical Leaders, Senior Analysts, Analysts and Technicians assigned as their direct and indirect reports.
-Preparing, reviewing and approving any protocols.
-Ensuring laboratory cGMP procedures/systems are adhered to and investigate and manage any non-compliance issues.
On offer is a competitive salary plus excellent benefits (pension, healthcare, flexible working, childcare vouchers, free parking, health promotions, death in service benefits and more).
@
Qualifications, Skills and Experiences:
-BSc (or equivalent) in Chemistry or a Life Science subject with a significant chemistry portion.
-Significant experience of leading analytical activities for Pharmaceutical drug products in a cGMP environment.
-Significant experience of Analytical method development, this must include a high level of HPLC, Analytical Validation, this must include a high level of HPLC and Stability study design and testing.
-A good understanding of the pharmaceutical drug development process from an analytical perspective.
Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained.
CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 47001 in all correspondence.
INDGEN
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