Pharmaceutical Quality Control - Shift Analyst

Taylorollinson; Oxford; On-site; GBP 30,000 - 50,000; Full time

Job description

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.

The role:

As a QC Analyst, you will be responsible for analysing pharmaceutical samples using a range of analytical techniques for a variety of projects. All work must be carried out 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.

Experience expectations:

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

The Package:

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.