The Regulatory group works with the wider business to translate the constantly evolving requirements of the UK Regulatory environment into the clients policies, procedures, solutions and strategies that ensure compliance and maximize the value for patients.
Do you possess a strong understanding of medical device regulations, coupled with at least 3 years' experience in medical device regulatory affairs and MDR?
We are a global wound care manufacturer, looking to appoint a knowledgeable and experienced Regulatory Affairs Specialist to our growing team.
As regulation around the smart metering infrastructure continues to evolve, we need to stay informed and proactive in lobbying to ensure the interests of meter asset providers are considered.
Calisen is the UK's leading meter asset provider for smart meters.
Our growth strategy spans low carbon heating solutions, solar and battery offerings, electric vehicle charge points, and water meters.
An exciting opportunity for a German Speaking candidate with a background in Specifications and Artwork approval to join this highly successful business that provide labelling, consumer information and regulatory advice.
OPPORTUNITY HIGHLIGHTS
Fully remote role.
This role is for a fluent German Speaking candidate only.
We are seeking a highly knowledgeable and experienced Regulatory Reporting Compliance Advisor on a contract basis to join the compliance advisory team.
This role involves reviewing requirements, advising on regulatory interpretation and practice, control design, and resolving queries from the First Line of Defense (1LOD) regulatory reporting teams.
The ideal candidate will focus on key regulatory frameworks, including MiFID II, EMIR, and SFTR, providing interpretative and advisory support to our regulatory reporting colleagues.