Regulatory Affairs Specialist - Remote/Watford Head Office Based

Are you an expert in Medical Devices Regulations who seeks an opportunity to join a leading and fast-growing company within the Global Ophthalmology Market?
Our client is seeking a Regulatory Affairs Specialist to work on a hybrid basis, working at least 2 days in Head Office in Hertfordshire.
The ideal candidate will work across all therapy areas of their extensive product portfolio, forming an integral part of the Regulatory Team.

Ideal Requirements
At least 2-3 years of regulatory knowledge including a solid understanding of the EUMDR 
Post market experience 
Competent in Microsoft Office suite 
Experience in medical devices 
Field Safety Corrective Action experience

Role Responsibilities
Stay well-informed of regulatory changes and liaising with Regulatory and Quality contacts in EMEA and Corporate to ensure UK and Ireland regulatory requirements are met and procedures updated accordingly 
Undertake Post Market Surveillance (PMS) activities in the region, including the execution of Product Field Safety Corrective Actions (FSCA)  
Provide training and education on Regulatory Affairs topics both internally and externally as required 
Resolve regulatory inquiries from both internal and external stakeholders

Role Specific Competencies
Collaborative and positive spirit
Adaptable and open for change 
Strong communication skills
Ability to work to tight timelines

Recruitment Process
2/3 stage process.

Interested? Please click apply or contact Claire Handley on 0113 457 0777 to discuss further!

Evolve is a leading recruitment and outsourcing organisation, operating within the Pharmaceutical, Healthcare, Medical Device and Life Science sectors.