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QC Analyst

Smart4Sciences
Posted 7 hours ago, valid for a month
Location

Preston, Lancashire PR4 0AS, England

Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • The role of QC Analyst is available in Preston with a salary of up to £28,000.
  • Candidates must have a relevant science degree or equivalent qualification and experience in analytical validation.
  • The position involves designing and conducting HPLC/UPLC/UV/GC analytical method validation and supporting quality monitoring processes.
  • A strong understanding of GMP, Health and Safety, and COSHH regulations is required for this role.
  • The ideal candidate will have relevant experience in a pharmaceutical or equivalent laboratory environment.

Role: QC Analyst

Location: Preston

Full time

Salary: Up to £28,000

A fantastic opportunity has arisen for a QC Analysts to join a sterile manufacturing facility in North Wales. We offer a fantastic package plus benefits such as:

  • 7 % matched pension
  • Discounts on common retail outlets through our rewards platform
  • Generous holidays
  • Salary sacrifice scheme
  • Subsidised canteen
  • Free parking

The role: QC Analyst

As an Analyst you will:

  • Design and carry out HPLC/UPLC/UV/GC analytical method validation and/or verification
  • Support the department to monitor the quality of components, raw materials, products and production processes by inspection, sampling and/or analysis.

The successful QC Analyst will have:

  • A relevant science degree or equivalent qualification
  • Understanding of current GMP, Health and Safety and COSHH regulations
  • Experience of designing validation, and/or verification protocols, running method validation, and/or verification studies and be able to write validation reports with minimal supervision
  • The ability to take on a limited supervisory role would be an advantage
  • Relevant experience in a pharmaceutical or equivalent laboratory environment and proven industry experience performing analytical validation

To apply for the Senior Quality Control Analyst or here more information, please contact Jack Challinor at Smart4Sciecnes on

Apply now in a few quick clicks

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.