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Pharmaceutical Quality Control Analyst

taylorollinson Ltd
Posted 18 hours ago, valid for 23 days
Location

Kidlington, Oxfordshire OX5 2XY

Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • The job is for a Pharmaceutical Quality Control Analyst located in Oxfordshire with a leading Pharmaceutical CRO.
  • The role involves analyzing pharmaceutical samples using various analytical techniques and ensuring compliance with industry standards.
  • Applicants must have previous experience in the pharmaceutical industry, specifically in analytical or QC roles, and at least 2-3 years of relevant experience.
  • Candidates should be familiar with techniques such as HPLC, GC, NMR, UV-Vis, and FT-IR, as well as GMP, FDA, and MHRA guidelines.
  • The position offers a competitive annual salary and benefits for a permanent role within the company.

Pharmaceutical Quality Control 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

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 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

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.

Apply now in a few quick clicks

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.