HRjob8409 Quality Control Supervisor - Edinburgh, United Kingdom - Almac Group

Almac Group
Almac Group
Verified Company
Edinburgh, United Kingdom

1 week ago

Tom O´Connor

Posted by:

Tom O´Connor

beBee Recruiter
Description

Quality Control Supervisor

Hours: 40 hours per week


Salary:
Competitive


Ref No:
HRJOB8409


Business Unit:
Almac Sciences


Location:
Technopole, Edinburgh


Open To:
Internal and External Applicants may apply


The Business Unit


Almac Sciences provides a wide range of custom synthesis services, technology, and products to the pharmaceutical industry, supporting our clients from drug discovery to commercialisation of new chemical entities.

We can offer a complete set of solutions aimed at accelerating entry into early-stage clinical development.


The Role
Almac Sciences, Edinburgh, are now recruiting for a Quality Control Supervisor.

The post holder will be responsible for providing hands-on technical leadership in the support of high throughput GMP manufacturing projects, testing and release of finished product, raw materials, and other QC related tasks.


The QC Supervisor will participate in site scheduling meetings and be responsible for scheduling and assigning analysis required to support client manufactures and related stability programs, ensuring all required analysis is performed correctly and on time.


They will also provide technical and chromatographic expertise in method validation exercises undertaken for new clients and ensure relevant protocols and reports are in place.


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.


Essential

  • GCSE (or equivalent) passes, grades A-C, in Mathematics and English Language
  • Degree level qualification (or equivalent) in a Life Science related discipline
  • Previous analytical experience within the pharmaceutical or fine chemical industries.
  • Working knowledge of HPLC and mass spectrometry.

Desirable

  • Degree level qualification (or equivalent) in an Analytical related discipline
  • LCMS experience
  • Experience of drug substance and/or drug product analysis in a GMP environment
  • Experience in HPLC method development and/or tech transfer and/or validation
  • Experience in supervising staff

Closing Date:
Tuesday 28th February 2023 at 5pm
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