QC Analyst

QCS Staffing; England; On-site; GBP 30,000 - 50,000; Full time

Job summary

Join a global bio-pharmaceutical company as a QC Analyst in a groundbreaking project in the UK. This role involves performing critical analytical chemistry and stability testing using advanced techniques like HPLC and UPLC. You will be integral to maintaining cGMP standards, managing laboratory supplies, and ensuring a safe working environment. This innovative firm is at the forefront of biotechnology, offering a unique opportunity to contribute to revolutionary products. If you're passionate about quality control in a fast-paced environment, this is the perfect role for you.

Qualifications

• Experience in analytical chemistry and stability testing.
• Knowledge of laboratory safety and cGMP practices.

Responsibilities

• Conduct routine analytical testing and maintain documentation.
• Manage laboratory supplies and ensure a safe working environment.

Skills

HPLC

UPLC

GC

UV Spectroscopy

Dynamic Light Scattering

cGMP Documentation

LIMS (LabVantage)

Education

BA/BSc in Chemistry

Relevant scientific discipline

Tools

LIMS

Job description

QC Analyst - Oxfordshire, England - 6 Months Contract

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

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

Essential Duties and Responsibilities:

1. Performs routine analytical chemistry & stability testing including, but not limited to, HPLC, UPLC, GC, UV, Particle Analysis by Dynamic Light Scattering, KF, etc.
2. Performs HPLC (AEX) and NaOH plate reader-based assays in support of manufacturing process stat testing as needed.
3. Completes and maintains cGMP documentation for work performed.
4. Performs general laboratory support activities including reagent preparation, sample management, equipment maintenance, lab housekeeping, etc.
5. Establishes and maintains a safe laboratory working environment.
6. Enters sample results into LIMS (LabVantage) and executes Electronic Assay Forms in LIMS.
7. Assists with and executes ordering of laboratory consumables and supplies; manages and stocks QC lab supplies.
8. Performs stability responsibilities in compliance with SOPs and supports stability programs.
9. Creates, reviews, and revises stability protocols and reports.
10. Supports stability set-down and pull activities, including labelling, verifying sample quantities, and updating in LIMS and logs; manages routine stability sample inventory, assessment, and disposal activities.

Desirable Experience:

• BA/BSc in Chemistry (preferred) or other relevant scientific discipline.
• Extensive experience in a quality control laboratory within a pharmaceutical company.

If you would like to apply or find out more, get in touch now!