We’re offering…
A stimulating and rewarding quality role in the MEU’s phase 1 accredited unit in Wythenshawe and its sister company, CRO Solutions in Salford Quays. This is an ideal opportunity to gain further experience in a regulatory environment, with the potential for progression as the company grows.
The role…
You will be an enthusiastic, self-motivated, organised quality professional with a keen eye for detail. Some previous experience (ideally between 1 – 2 years) of working in a GCP regulated environment or in a quality environment in a clinical trial organisation is desirable.
Day to day, you will oversee the Company’s quality systems, including the management of SOPs, deviations, change controls and CAPAs. You will also conduct internal and vendor audits in accordance with the approved audit programme and host Sponsor audits and regulatory inspections, as required.
You will also have a high level of competence in Microsoft Office and the ability to communicate effectively with all levels of staff. A science background would be advantageous but is not essential for the right person.
This is an office-based position in Manchester. A full UK driving licence is required.
We will offer you……
CRO-Solutions® is our sister company to Medicines Evaluation Unit Ltd. Located at Salford Quays, CRO-Solutions® has the ability to offer a single site solution for all your clinical trial needs.
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