QC Analyst - Method Development - North East

A chance for a motivated and experienced QC Analyst to join a chemical research and development company in the North East. As a QC Analyst you will be responsible for developing methods using HPLC and GC in a busy R&D environment and ensuring that products meet the highest standards of quality and accuracy. If you are a QC Analyst and have prior experience in method development then apply below!

Key Responsibilities as a QC Analyst

• Develop, optimise and validate HPLC and GC methods of raw materials and intermediates
• Conduct routine analysis of samples using HPLC and GC, and other techniques such as KF, NMR and MS
• Analyse and interpret data
• Contribute to instrument maintenance, troubleshooting instruments when required

Key Requirements for a QC Analyst

• Degree educated in Chemistry or a related subject
• A minimum of 2 years of experience in HPLC and GC method development and validation
• Familiarity with GMP regulations and regulatory requirements
• Previous analytical experience within the chemicals or pharmaceuticals industry

Apply immediately with a CV (In Word document format) to be considered for this great opportunity.

Note my client is unable to sponsor visas for those without eligibility to work in the UK.