Regulatory Affairs Specialist

In the context of a new project, we are looking for a Regulatory Affairs Specialist to join our teams in Mexico. Group Responsibilities Provide guidance and support about Mexican and Central America legislation Contribute to the regulatory activities performed. Regulatory activities include pre licensing activities, new registration (sites and medicinal products), post licensing regulatory submissions. Contribute to the production of client administrative documents to be included in regulatory submissions Compile regulatory dossiers in accordance with national requirements. Systems Management and Administration Document and track regulatory submissions and regulatory authority approval. Provide regulatory support to clients and associate companies Liaise with sponsor head-Office and affiliate departments on regulatory issues. Provide review of packaging texts. Provide format review of Summary of Product Characteristics, Patient Information Leaflets, and labelling (e.G., QRD compliance check). Contribute to data entry in PLG tools enabling measurements of KPI, metrics for regulatoryservices Group Education & Experience Bachelors degree or more in a Life Sciences related field. Pharmacy degree would be a plus. 4-8 years of experience in Regulatory Affairs in the Pharmaceutical Industry or via a Service Provider Previous experience in a consulting company would be a plus Group Profile Hard/Technical skills:
Excellent organizational and interpersonal skills Autonomous Excellent communication skills Ability to work well within a team and autonomously Ability to prioritize different workloads/multi-task Process orientated with good attention to detail Solution-driven