Global Regulatory Affairs Associate - Hybrid (EMEA)

Recruitment Solutions (Folkestone) Limited; Folkestone; Hybrid; GBP 21,000 - 39,000; Full time

Job summary

Recruitment Solutions (Folkestone) Limited is seeking a Regulatory Affairs Associate on a temporary contract based in Folkestone. You will support regulatory compliance and product registrations across EMEA, collaborating with internal teams and distributors to ensure timely market access.

The role requires strong regulatory knowledge, project management and stakeholder communication. Hybrid working is offered, with exposure to medical devices, medicines and consumer healthcare products.

Qualifications

• Good understanding of EU MDR 2017/745 and regulatory requirements.
• Strong organisational and project management skills.
• Excellent attention to detail and accuracy.
• Strong written and verbal communication and relationship-building.
• Proactive, self-motivated with ability to work independently.
• Experience in Regulatory Affairs, product registrations or compliance.

Responsibilities

• Support regulatory enquiries and product registration activities with internal teams and distributors.
• Prepare, coordinate and submit documentation for new registrations and licence maintenance.
• Research and apply regulatory requirements across EMEA markets.
• Collaborate with Quality, R&D, Marketing, Supply Chain and Legal to maintain regulatory dossiers.
• Manage registration projects and ensure milestones are met.
• Maintain regulatory files and coordinate signings, authentication and legalisation.
• Liaise with authorities and stakeholders to support market access.

Skills

Regulatory affairs

Project management

Communication

Attention to detail

Stakeholder management

Analytical thinking

Tools

Microsoft Office

Word

Excel

Teams

SharePoint

Job description

Recruitment Solutions (Folkestone) Limited is seeking a Regulatory Affairs Associate on a temporary contract based in Folkestone. You will support regulatory compliance and product registrations across EMEA, collaborating with internal teams and distributors to ensure timely market access.

The role requires strong regulatory knowledge, project management and stakeholder communication. Hybrid working is offered, with exposure to medical devices, medicines and consumer healthcare products.