Pharmaceutical Quality Control Analyst - Validation

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

Job summary

A leading Pharmaceutical company in Oxfordshire is seeking an experienced Pharmaceutical Quality Control Analyst to support validation studies within their analytical team. The successful candidate will analyze pharmaceutical samples using various techniques and must possess previous experience in the pharmaceutical industry. This role offers a competitive salary and opportunities for career progression.

Benefits

Competitive annual salary

Benefits

Career progression opportunities

Qualifications

• Previous Pharmaceutical industry experience in an analytical or QC role is essential.
• Experienced in the use of analytical techniques such as HPLC, GC, NMR, UV-Vis, FT-IR.
• Good knowledge of GMP, FDA and MHRA guidelines.

Responsibilities

• Analyse pharmaceutical samples using a range of analytical techniques.
• Validation and verification of analytical methods.
• Carry out degradation and stability studies.

Skills

Analytical techniques (HPLC, GC, NMR)

Quantitative and Qualitative analysis

Good communication skills

Organised and methodical approach

Education

Degree in Analytical Chemistry, Pharmaceutical Science or Chemistry

Tools

HPLC

GC

NMR

Job description

Overview

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.

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 / Benefits

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.

Eligibility

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.