Myonex is seeking a Quality Operations & Systems Specialist (Maternity Cover) to join our team in Leicester, from 1st August 2026 to 30th September 2027. If you have experience within a GxP pharmaceutical environment, we want to hear from you!
About Myonex:
Myonex is a leader in providing integrated clinical and commercial services to support the advancement of life-saving medicine.
We partner with pharmaceutical, biotechs, and contract research organizations (CROs) in both clinical and commercial stages, including companies managing advanced therapies. With locations in the US, Germany, UK and France, Myonex supports projects globally.
Built in 2017, Myonex Leicester, our UK clinical trial storage and distribution facilities, manages both IMP/NIMP and equipment supplies. The local teams work in tandem with the other Myonex facilities for seamless clinical trial supply sourcing and distribution across Europe, particularly taking into account the impact of Brexit and QP oversight.
The Benefits:
* Salary of £36,000 - £42,000.
* 7.5% performance-related bonus.
* Salary sacrifice, 2-1 contribution pension scheme.
* Private medical insurance (after the qualifying period).
* Fast-paced, team-oriented environment.
* Progression and development opportunities.
About the Role:
As the Quality Operations & Systems Specialist, you carry out day‑to‑day QC activities which are supportive of both business and compliance needs of Myonex Ltd. The role is responsible for reviewing and approving clinical trial project set‑up documentation, including protocols, applications, ethics approvals, and Quality Technical Agreements. The role delivers hands‑on Quality Control activities, completing QC checks on GxP materials, Just‑In‑Time labelling processes, and outbound clinical shipments, while supporting transport risk assessments. You will draft and maintain Product Specification File indices, issue packaging materials, and ensure accurate stock movements and releases within the Oracle Cloud ERP system. The position works closely with internal stakeholders to support the import of EU QP‑certified material into Great Britain, reviewing both internal and client documentation. You will also generate regulatory reports for imported batches, approve key vendor purchase orders, and provide back‑up support for returns and destruction activities as required.
About the Candidate:
* Experience within a GxP pharmaceutical environment and QA experience
* Excellent organisational and communication skills (both written and verbal).
* Accuracy and detail oriented.
* Ability to multi-task.
* Experience with Microsoft Office packages.
* Relevant university degree or equivalent preferred.
* Experience within the Clinical Trial environment
* Experience of eQMS and ERP systems
Most important of all, your values will align with ours: you will Be a Great Team Player, Be Client Focused and you will always strive to Learn & Grow and Find a Way. Join us at Myonex and contribute to our mission of delivering excellence in the clinical trials space.
This organisation is an equal opportunities employer who welcomes applications from underrepresented groups. We are happy to discuss any reasonable adjustments individuals may require in the recruitment process, on commencement, or once in post.
To find out more about what Myonex do and who we are as an employer, head to our LinkedIn page and website.
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