Pharmaceutical Quality Control - Shift Analyst

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

Job summary

Une entreprise pharmaceutique de premier plan basée en Oxfordshire recherche un Analyste de Contrôle Qualité pour rejoindre son équipe. Ce poste basé sur un système de rotation de 12 heures vous demandera d'analyser des échantillons en utilisant diverses techniques analytiques tout en respectant les normes de qualité et les réglementations de l'industrie. Une expérience antérieure dans un rôle analytique ou QC est essentielle, et vous serez responsable de documenter chaque étape du processus. Ce rôle comprend une rémunération concurrentielle et un ensemble d'avantages attrayants.

Benefits

Salaire annuel compétitif

Avantages sociaux

Primes de rotation généreuses

Qualifications

• Expérience antérieure dans l'industrie pharmaceutique en rôle analytique ou QC requise.
• Compétences dans l'utilisation de techniques analytiques comme HPLC et GC.
• Connaissance des lignes directrices GMP, FDA et MHRA.

Responsibilities

• Analyser des échantillons pharmaceutiques en utilisant diverses techniques analytiques.
• Assurer la conformité avec les normes de qualité et les lignes directrices de l'industrie.
• Documenter et rapporter le travail de laboratoire effectué.

Skills

Analyse Quantitative

Analyse Qualitative

Connaissance de GMP

Utilisation de HPLC

Utilisation de GC

Utilisation de NMR

Utilisation de UV-Vis

Utilisation de FT-IR

Education

Diplôme en Chimie Analytique, Science Pharmaceutique ou Discipline Connexe

Job description

Pharmaceutical Quality Control - Shift Analyst

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

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.

I'm interested in this job

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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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