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An established industry player is seeking a motivated Quality Administrator to support the Product Development/QMS team. This full-time role offers the opportunity to work in a hybrid model, ensuring compliance with GxP regulations. You will assist with the administration of the eQMS, support training initiatives, and manage supplier qualifications. Join a collaborative and high-performing environment where your contributions will help shape the future of a fast-growing business. If you are self-motivated and detail-oriented, this is a fantastic opportunity to make a significant impact in a dynamic team.
Cycle Pharmaceuticals based in Cambridge are seeking motivated Quality Administrator. As a Quality Administrator, you will be responsible for providing administrative support for the Product Development/QMS team to maximise quality and efficiency and ensure compliance with relevant GxP regulations (GMP, GDP, GCP and GVP).
Job Interactions & Interface:
This role interacts internally with key areas such as Regulatory – CMC, Clinical and Product Development, Supply Chain, Project Management, Legal and Finance. Externally this position interacts with service suppliers and contractors.
Position Summary: This is a full-time position within the Quality department, working in our Cambridge office on a hybrid basis (minimum 3 days in the office).
Key Responsibilities:
Qualifications and Skills:
What can we offer to you:
Applications: Cycle Pharmaceuticals embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.