Pharmaceutical Quality Control - Shift Analyst

ZipRecruiter; Oxford; On-site; GBP 80,000 - 100,000; Full time

Job summary

A leading Pharmaceutical CRO in Oxford is seeking an experienced QC Analyst for a shift-based position. The role involves analyzing pharmaceutical samples using a variety of analytical techniques while ensuring compliance with quality standards. Ideal candidates should possess relevant experience in the pharmaceutical industry, good communication skills, and a degree in a related field. Competitive salary and benefits are offered.

Benefits

Competitive annual salary

Generous shift allowance

Opportunity for permanent employment

Qualifications

• Previous experience in the pharmaceutical industry in an analytical or QC role is essential.
• Experience in using various analytical techniques.
• Good knowledge of GMP, FDA, and MHRA guidelines.

Responsibilities

• Responsible for analyzing pharmaceutical samples using a range of analytical techniques.
• Ensure all work meets the highest quality standards and complies with industry guidelines.
• Report and provide written documentation for laboratory work.

Skills

Analytical techniques

Communication skills

Organised and methodical approach

Education

Degree in Analytical Chemistry, Pharmaceutical Science or Chemistry discipline

Tools

HPLC

GC

NMR

UV-Vis

FT-IR

Job description

Overview

Pharmaceutical Quality Control - Shift Analyst

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.

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. 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 / 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
• 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

Package / Benefits

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. 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