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Pharmaceutical Quality Control Analyst - Validation
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 and support in Validation studies within the analytical team.
The role:
As a QC Analyst you will be responsible for analysing pharmaceutical samples using a range of analytical techniques and for a variety of projects.
This role will focus on:
- Validation and verification of analytical methods for HPLC, GC, NMR, KF etc.
- Degradation and stability studies for a variety of conditions
- LCMS analysis for impurity identification
- Running and reporting on multiple projects simultaneously
- All work must be carried to the highest quality standards and in compliance with industry guidelines.
- You will also be expected to interpret and report on the laboratory work completed.
Experience expectations:
Suitable applicants;
- 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
- Experience with Method Validation and Stability studies
- Educated to degree level (or equivalent experience) in Analytical Chemistry, Pharmaceutical Science or Chemistry discipline
- Organised and methodical approach to work
- 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 career progression opportunities.
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.
