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.
#J-18808-Ljbffr