Job Description

• North West
• \xc2\xa360,000-\xc2\xa375,000 + bonus
• Non-Laboratory & Other Scientific Roles

About this job

Rare opportunity for an accomplished Quality Manager to take the next step up to Director level!

Our client offers a fully integrated scientific and regulatory consultancy service to the global pharmaceutical and nicotine/cannabinoids market, combined with comprehensive laboratory services. Joining the company as Associate Director of Quality, you will hold ultimate responsibility for quality and compliance across two busy laboratory sites undertaking GMP, GLP, ISO and non-GxP regulated projects. You will play a key role in the implementation of GMP regulations, ensuring a harmonised QMS system across both sites and the wider remote team. Utilising previous experience, you will directly manage a team of 4 Quality Managers within a quality department of 9 professionals.

A clear progression route to Quality Director has been carved for the successful incumbent within 12 months.

Applications are invited from Quality Managers from a GMP, GLP or ISO17025 environment. You will be skilled in managing a team of quality professionals and have confidence and determination to excel at Director level.

In return you will receive a competitive salary and extensive benefits package, with up to 10% OTE bonus, rising to 20% upon promotion to Director level. This is a site-based role, with flexibility for 1 day per week home working.

Apply now to be considered!

Keywords: Quality, Management, Manager, Director, Associate, QM, QMS, laboratory, pharmaceutical, GMP, GLP, GxP, ISO, ISO17025, nicotine, cannabinoids, chemistry, analytical, HPLC, Lancashire, North Yorkshire, Skipton, Earby, VRS8437AW

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