Method Validation Analyst

Industry Sector Pharmaceutical
Location UK, South East
Salary Competitive

Description

Method Validation Analyst

Location: Oxfordshire

Sector: Pharmaceutical

Our client is a leading Pharmaceutical CRO based in Oxfordshire and due to continued expansion they now seeking an experienced analyst within their Quality Control department with a particular focus on validation of analytical methods.

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. 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.

Experience expectations:

Suitable applicants;

·       Previous Pharmaceutical industry experience working in an analytical or QC role would be beneficial

·       Experience in the validation of analytical methods

·       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

·       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.

 

For additional information or to submit an application please contact Sam Coxon on 07789 695548 or email your CV and cover letter to sam.coxon@taylorollinson.co.uk

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