At a Glance
- Tasks: Manage documentation and support compliance processes in a detail-oriented role.
- Company: Join a dynamic, growing orthopaedics company with a supportive team culture.
- Benefits: Flexible part-time hours that fit around your life and studies.
- Other info: Perfect for team players who thrive in a collaborative environment.
- Why this job: Make a real impact in quality and regulatory compliance while gaining valuable experience.
- Qualifications: Experience in a regulatory or quality-focused admin role is essential.
The predicted salary is between 24750 - 30250 £ per year.
This is a part-time position, between 16-20 hours a week. You’re comfortable working where detail matters. Managing documentation, supporting compliance processes, and keeping quality systems running smoothly behind the scenes. You’ve built experience in a regulatory or quality-focused admin role, and you take pride in keeping things accurate, organised, and audit-ready. This role gives you a chance to use that experience, and – because it’s a part-time role – it’ll also work around you and your life. It's perfect for someone who wants a role that fits with school hours, or over fewer days per week. As long as you can get the job done, it'll fit around your life, not the other way round.
And it’s not just the hours that make this a great fit. You’ll be joining a tight-knit, growing orthopaedics business that’s growing steadily. The team’s supportive and collaborative, so you’ll be surrounded by people who help each other out.
What will your day to day look like? You’ll support the quality and regulatory teams with keeping their processes and procedure in good shape. An average week might include:
- Ensuring processes related to quality/regulatory compliance are maintained
- Managing the document control process
- Updating policies, procedures and forms relating to QMS and regulatory compliance
- Administering the CAPA process for the business
- Coordinating the internal IL process, including managing updates and handling complaints
- Administering any product recall activities
- Monitoring MHRA field safe notices
- Compiling information required for quality management reviews
- Assisting with product registrations
This role will suit you if you…
- Have experience in an ISO13485 or ISO9001 certified business (or other regulated industry)
- Have an internal audit qualification or experience performing them
- Are great at admin, communication and time management
- Love getting into the nitty gritty and thrive on detail
Think this could be your next role? Then we’d love to hear from you!
Regulatory Affairs & QMS Administrator in England employer: FMC Talent
Join a dynamic and fast-scaling software company that prioritises employee growth and rewards performance in a meritocratic environment. With the flexibility of remote or hybrid work options in Leeds, you will benefit from uncapped commission structures and a supportive culture that fosters collaboration and innovation. This role not only offers competitive compensation but also the opportunity to make a significant impact in asset-intensive industries, ensuring your contributions are recognised and valued.
