QC Analyst

QCS Staffing; England; On-site; GBP 25,000 - 35,000; Full time

Job summary

A leading global biopharmaceutical company is seeking a QC Analyst for a 6-month contract in Oxfordshire. The role involves performing analytical chemistry and stability testing, maintaining cGMP documentation, and supporting laboratory activities. Ideal candidates will have a BSc in Chemistry and relevant experience in a pharmaceutical quality control setting.

Qualifications

• BSc in Chemistry or relevant scientific discipline.
• Extensive experience in a pharmaceutical quality control laboratory.

Responsibilities

• Perform routine analytical chemistry & stability testing.
• Maintain cGMP documentation for all work performed.
• Support general laboratory activities and establish a safe laboratory environment.

Skills

Analytical Chemistry

HPLC

UPLC

GC

UV

Dynamic Light Scattering

Education

BSc in Chemistry

Tools

LIMS (LabVantage)

Job description

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QC Analyst - Oxfordshire, England - 6 Months Contract

Would you be interested in working for a global biopharmaceutical company supporting a state-of-the-art new-build project in the UK?

Are you a QC Analyst based in the UK seeking an opportunity with one of the world’s leading biotechnology companies? We have the role for you! Our client is at the forefront of developing key and revolutionary products, and with a thriving global presence, they are recruiting a QC Analyst to join their new project.

Essential Duties and Responsibilities:

• Perform routine analytical chemistry & stability testing, including HPLC, UPLC, GC, UV, Particle Analysis by Dynamic Light Scattering, KF, etc.
• Conduct HPLC (AEX) and NaOH plate reader-based assays to support manufacturing process stat testing.
• Maintain cGMP documentation for all work performed.
• Support general laboratory activities such as reagent preparation, sample management, equipment maintenance, and lab housekeeping.
• Establish and uphold a safe laboratory environment.
• Enter sample results into LIMS (LabVantage) and execute Electronic Assay Forms.
• Manage ordering of laboratory consumables and supplies, and oversee QC lab stock.
• Perform stability testing in compliance with SOPs and support stability programs.
• Create, review, and revise stability protocols and reports.
• Assist with stability sample setup, labeling, quantity verification, and updates in LIMS; manage routine stability sample inventory, assessment, and disposal activities.

Desirable Experience:

• BSc in Chemistry or a relevant scientific discipline.
• Extensive experience in a pharmaceutical quality control laboratory.

If you're interested in applying or learning more, get in touch now!

Additional Details:

• Seniority level: Entry level
• Employment type: Contract
• Job function: Quality Assurance
• Industries: Staffing and Recruiting