Pharmaceutical Quality Control Analyst Validation

taylorollinson Ltd; United Kingdom; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading Pharmaceutical CRO in Oxfordshire is seeking a Pharmaceutical Quality Control Analyst for validation studies. The role involves analyzing samples with techniques like HPLC and GC, ensuring compliance with industry standards. Candidates should have a degree and experience in the pharmaceutical sector.

Qualifications

• Previous experience in a pharmaceutical analytical or QC role is essential.
• Knowledge of quantitative and qualitative analysis required.
• Organised and methodical approach to work.

Responsibilities

• Analyze pharmaceutical samples using various analytical techniques.
• Perform validation and verification of analytical methods.
• Report on stability studies and laboratory work.

Skills

Analytical Chemistry

GC

HPLC

NMR

Method Validation

GMP

FDA Guidelines

Education

Degree in Analytical Chemistry

Pharmaceutical Science

Job description

Pharmaceutical Quality Control Analyst Validation

Pharmaceutical 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.

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.

This role will focus on:

• 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 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
• 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

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 career progression opportunities.

Applicants 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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Compulsory fields are in bold.

I'm interested in this job

Please use the form provided to get in touch with us and we will respond as soon as possible.

Compulsory fields are in bold.

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