OverviewPharmaceutical 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.

Responsibilities

As a QC Analyst you will be responsible for analysing pharmaceutical samples using a range of analytical techniques and for a variety of projects.

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 / Qualifications

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

Package / BenefitsOur 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.

EligibilityApplicants 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.

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