Pharmaceutical Quality Control Supervisor

Industry Sector Pharmaceutical
Location UK, South East
Salary Competitive

Description

Pharmaceutical Quality Control Supervisor 

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 Supervisor to join the company

 

The role: 

As a QC Supervisor you will be responsible for overseeing a team and facilitating the analysis of pharmaceutical samples using a range of analytical techniques. Working in a CRO environment you will need to be able to support on various pharmaceutical analysis projects and provide technical guidance on analytical techniques, including troubleshooting, maintenance and development of analytical methods. 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 experience in a supervisory role within a pharmaceutical analytical team, ideally within a CRO and/or GMP environment

·       Significant experience in the use of analytical techniques such as HPLC, GC, NMR, UV-Vis, FT-IR

·       Experience in method development and validation

·       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 and benefits.

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