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Smart4Sciences are currently working with a Pharmaceutical Company in the North West to recruit a QA Officer to join a small team responsible for all aspects GMP compliance within their Sterile manufacturing facility on a 12 month fixed term contract.

This QA Officer position is a brilliant opportunity for candidates with prior GMP experience to further their career within QA with a company who can provide strong progression opportunities or for people with a background in GMP laboratories who are keen to transition to QA.

Key Responsibilities

Respond to and action quality enquiries and quality management activities including deviations, change controls, risk assessments, complaints etc.Support internal and external GDP/GMP auditsAuthor, review and archive quality documentation including SOPs, PQRs, supplier agreementsEnsure GMP compliance at all times

Key Requirements

Prior GMP experience within the pharmaceutical/medical device industries is essentialPrior experience working with Pharmaceutical Quality Management Systems is essentialA pro-active, can do attitude is essential

Interviews for this QA Officer position are imminent so please apply now or contact Gareth Gooley at Smart4Sciences for more information

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Role: QC Analyst

Location: Preston

Full time

Salary: Up to £28,000

A fantastic opportunity has arisen for a QC Analysts to join a sterile manufacturing facility in North Wales. We offer a fantastic package plus benefits such as:

7 % matched pensionDiscounts on common retail outlets through our rewards platformGenerous holidaysSalary sacrifice schemeSubsidised canteenFree parking

The role: QC Analyst

As an Analyst you will:

Design and carry out HPLC/UPLC/UV/GC analytical method validation and/or verificationSupport the department to monitor the quality of components, raw materials, products and production processes by inspection, sampling and/or analysis.

The successful QC Analyst will have:

A relevant science degree or equivalent qualificationUnderstanding of current GMP, Health and Safety and COSHH regulationsExperience of designing validation, and/or verification protocols, running method validation, and/or verification studies and be able to write validation reports with minimal supervisionThe ability to take on a limited supervisory role would be an advantageRelevant experience in a pharmaceutical or equivalent laboratory environment and proven industry experience performing analytical validation

To apply for the Senior Quality Control Analyst or here more information, please contact Jack Challinor at Smart4Sciecnes on

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