Regulatory Affairs Associate

Job Title: Regulatory Affairs Associate

Client: Hunter Selection

Location: Caerphilly, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference: 7791c6ab59d6

Job Views: 16

Posted: 14.03.2025

Expiry Date: 28.04.2025

Job Description

Are you passionate about delivering solutions to customers which deliver a genuine positive impact? This could be the perfect opportunity for you. My client is an international business with a strong market presence within their sector. They are looking to add a vital acquisition of a Regulatory Affairs Associate to the regulatory team. This role will provide you with a hybrid working model and the opportunity to develop your skillset within a highly regulated industry.

Roles and Responsibilities

• Support RA Director for regulatory documentation including updating technical files, reports, and procedures.
• Compile vigilance PMS and PSUR reports.
• Documentational support for worldwide regulatory submissions.
• Assist with Competent Authority registrations including the MHRA and ECREP.
• Create Declarations of Conformity.
• Review and manage standards database.
• Support Management of Patents and Trademarks.
• Create and implement compliant Regulatory procedures.

Requirements

• The successful candidate will have experience working within regulatory affairs.
• The ideal background for this role would come from a highly regulated industry – medical, pharmaceutical.
• Experience of technical files, competent authority regulations.
• Experience working with quality management systems.

Suitable candidates should apply immediately by calling Jack Lavis for this vacancy – on 02920 894900 or by sending your CV directly to him.