Associate,RegulatoryAffairs

ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. We are looking for a dynamic person to join our in-house team as an Associate, Regulatory Affairs on a permanent basis. Join our team: you can be part of making a difference in peoples’ lives and experience a fulfilling and rewarding career! Main Job Tasks and Responsibilities: Support with new application for marketing authorization/renewal/variation of medicinal products, medical devices, cosmetics, food supplements for regulatory submission and follow-up closely on queries from HA through to approval Publishing and submission of products registration applications Coordination of activities ensuring product registration information is accurate and current Support compilation, tracking, indexing and archival of regulatory information Specifying storage, labelling and packaging requirements for regulated products Creation, update, review and quality check of product labels Education and Experience: Bachelor’s Degree in Life Science (Chemistry, Biology, Biomedical Engineering) Experience in the related field is a plus Fluency in English Ability to work under pressure to meet the deadlines Ability to get a challenge and perform excellent teamwork Our Benefits: Flexible Working Hours Full performance and development process with end of year reviews Team events and end of year party Employee satisfaction survey - your feedback is important for continuous improvement Health Insurance The Application Process Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. Who will you be working for? About ClinChoice ClinChoice is a global full-se