Vacancy for Regulatory Affairs Executive (Lagos) at PACIFIC ACCESS

An indigenous Drugs manufacturing firm based in Isheri, Alimosho LGA of Lagos State, with regional centers and offices nationwide requires the services of Pharmacist to fit the following role in its employ;Regulatory Affairs Executive; Lagos.The Person MUST have minimum 2 years considerable experience in Research, Development and Regulatory affairs in relevant pharmaceutical industry. Must have performed internship or NYSC in any regulatory agency.Duties & Responsibilities:To manage the regulatory department and develop processes so that new chemical entities, new dosage forms and new indications are registered in a timely fashion. Overall responsibility for compiling regulatory submissions to NAFDAC and other regulatory bodies, drafting Product Information, Consumer Information, literature searches to support submissions, product analysis, changes in manufacturing, pack sizes, CPI and PI development, packaging changes, MIMS notification and other regulatory activities.Ensures that all state and federal regulatory requirements are addressed for the clinical research programme and for marketed products.Develop professional relationships with NAFDAC staff and proactively monitor relevant governmental bodies to identify changes in legislation/regulations.Provide regulatory expertise to clinical project teams (CTN applications, importation of clinical trial material, reporting of adverse events).Provide regulatory expertise to global product development teams.Conduct training sessions for CRAs and sales representatives on ADR reporting and the importance of pharmacovigilance.Working with marketing to ensure that the content of all promotional material is fully supported by the Product Information and literature, and in accordance with the guidance offered by NAFDAC and other government regulators.

Apply at