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Pharmaceutical Quality Control - Shift Analyst

Taylorollinson
Posted 2 days ago, valid for 23 days
Location

Oxford, Oxfordshire OX1 1HB, England

Salary

£40,000 - £48,000 per annum

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Contract type

Full Time

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Sonic Summary

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  • A leading Pharmaceutical CRO in Oxfordshire is seeking an experienced QC Analyst for a shift-based position involving 12-hour shifts on a 4 days on, 4 days off rotation.
  • The role involves analyzing pharmaceutical samples using various analytical techniques and ensuring compliance with industry standards.
  • Candidates must have previous experience in the pharmaceutical industry, particularly in analytical or QC roles, and be proficient in techniques such as HPLC, GC, NMR, UV-Vis, and FT-IR.
  • A degree in Analytical Chemistry, Pharmaceutical Science, or a related discipline is required, along with knowledge of GMP, FDA, and MHRA guidelines.
  • The position offers a competitive annual salary along with benefits and a generous shift allowance.

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 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, benefits and generous shift allowance.

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