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Senior QC Analyst

Smart4Sciences
Posted 2 days ago, valid for 2 days
Location

Wrexham, Wrexham LL144EJ, Wales

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 Senior QC Analyst is available in North Wales, Wrexham, offering a salary of around £30,000.
  • Candidates should possess a relevant science degree or equivalent qualification and have experience in designing validation protocols and performing analytical validation.
  • The position involves carrying out HPLC/UPLC/UV/GC analytical method validation and supporting quality monitoring processes.
  • Additional benefits include a 7% matched pension, generous holidays, and discounts on retail outlets.
  • Experience in a pharmaceutical or equivalent laboratory environment is required, along with an understanding of current GMP and Health and Safety regulations.

Role: Senior QC Analyst

Location: North Wales, Wrexham

Full time

Salary: Around £30,000

A fantastic opportunity has arisen for Senior 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.