Pharmaceutical Quality Control - Shift Analyst

Pharmaceutical Quality Control - Shift Analyst

Location:

Oxfordshire

Sector:
Pharmaceutical

Our client is a leading Pharmaceutical CRO based in Oxfordshire and, due to continued expansion, they now have an exciting opportunity for an experienced QC Analyst to join the company.

This role is a shift‑based position which includes 12 hour shifts on a 4 days on, 4 days off rotation.

As a QC Analyst you will be responsible for analysing pharmaceutical samples using a range of analytical techniques and for a variety of projects. All work must be carried to the highest quality standards and in compliance with industry guidelines. You will also be expected to report and provide written documentation for the laboratory work completed.

• Previous Pharmaceutical industry experience working in an analytical or QC role is essential
• Experienced in the use of analytical techniques such as HPLC, GC, NMR, UV-Vis, FT-IR
• Knowledge of Quantitative and Qualitative analysis
• Good knowledge of GMP, FDA and MHRA guidelines
• Educated to degree level (or equivalent experience) in Analytical Chemistry, Pharmaceutical Science or Chemistry discipline
• Any method development or method validation experience would be beneficial
• Organised and methodical approach to work
• Good communication skills

Our client offers an opportunity to work for a leading Pharmaceutical company on a permanent basis with a competitive annual salary, benefits and generous shift allowance.

Applicants must be fully eligible to work in the UK. Visa Sponsorship is not available with this position and therefore applicants must not require immediate sponsorship or have Visa sponsorship requirements in the future.