Join a dynamic team working with some of the most distinguished pharmaceutical companies in the UK and internationally.
We are looking for an experienced quality assurance professional to contribute to our continued success in the clinical trials sector.
About Us: The Medicines Evaluation Unit (MEU) is a phase 1 accredited unit based in Wythenshawe, and together with our sister company, CRO Solutions in Salford Quays, we are at the forefront of clinical research.
As our company enters its third expansion phase, we are offering a unique opportunity for a quality assurance professional to grow with us.
The Role: This stimulating role is ideal for someone with GCP (Good Clinical Practice) quality assurance experience in a regulatory environment.
You will play a key part in overseeing the company's quality systems, reviewing quality documentation, and managing deviations, change controls, and CAPAs (Corrective and Preventive Actions).
Please note, this is an on-site role based at our HQ in Wythenshawe, South Manchester.
Key responsibilities include: Conducting internal and vendor audits in accordance with the approved audit programme.
Hosting sponsor audits and regulatory inspections, as required.
Maintaining and improving the quality systems to ensure full compliance.
Writing clear and concise reports and communicating effectively with colleagues, vendors, and regulators.
You will need to be: Enthusiastic, self-motivated, and highly organized.
Experienced in working in a quality role within a clinical trial organization.
Proficient in Microsoft Office.
A good communicator with strong attention to detail.
A science background is advantageous but not essential.
A full UK driving licence is required, as the role involves travel between sites.
What We Offer: Starting salary dependent on experience.
Immediate start.
Continuous professional development opportunities.
29 days annual leave.
Company pension scheme.
Generous annual bonus.
Healthcare plan.
Free parking.