Regulatory Affairs Coordinator

Stannah is a family-owned manufacturing and engineering company. Our products move people and goods in and around homes and buildings. We make life easier for people. We do this by improving access for greater convenience and independence.

Stannah is a family-owned manufacturing and engineering company. Our products move people and goods in and around homes and buildings. We make life easier for people. We do this by improving access for greater convenience and independence. Joseph Stannah founded the business in 1867. A lot has happened since then and today Stannah is a global business. The family is in their fifth generation and plays a hands-on role in running the business.

Most people know us for our stairlifts. Our range of products includes lifts, escalators, and homelifts. We also provide maintenance and repair services.

Stannah have an exciting opportunity for a Regulatory Affairs Coordinator to join the Regulatory Affairs team based at our Andover Head Office
. This role will involve supporting the Head of Regulatory Affairs to ensure Stannah products comply with relevant legal, regulatory and internal policy requirements. You'll play a key role in maintaining regulatory records, coordinating testing and certification activities, supporting compliance initiatives and helping to ensure our product documentation remains accurate and up to date. As the Regulatory Affairs Coordinator
, you will work full-time hours on a permanent basis. The successful candidate can work on a hybrid basis after successful training with flexi-time working. This is a great opportunity for someone looking to build a career in regulatory affairs, compliance or quality within a global manufacturing business. With structured training and development provided, this role offers an excellent foundation for candidates with strong administration, organisation and attention to detail skills who are keen to develop specialist regulatory knowledge.

To be successful as the Regulatory Affairs Coordinator
, it is essential that you have strong organisational skills and attention to detail. Experience of Document Control within a manufacturing environment, ideally Medical Device manufacturing, would be highly desirable, as is knowledge of CE Marking. This is not a straightforward admin role, you will be working on multiple regulatory projects, and over time, it is expected that you will become familiar with various regulations and be comfortable working with them.

A willingness to learn is a prerequisite.

• Maintain and organise regulatory records, technical files, Declarations of Conformity and certification documentation.
• Support the creation, implementation and maintenance of regulatory processes, registers and tracking systems.
• Gather, collate and verify data for regulatory filings, registrations and compliance reporting.
• Coordinate testing and certification activities with external laboratories and certification bodies.
• Assist with regulatory monitoring, compliance training administration, audits and stakeholder communications.

Please see the full job description here:
Regulatory Affairs Coordinator

• Strong organisational skills with excellent attention to detail.
• Good written and verbal communication skills and proficiency in Microsoft Office applications.
• Ability to manage multiple priorities, maintain accurate records and meet deadlines.
• A proactive approach with a willingness to learn and develop knowledge of regulatory compliance and product legislation.

If you have previous experience…