Regulatory Affairs Pharmacist

Job title : Regulatory Affairs Pharmacist Job Location : Gauteng, Johannesburg Deadline : January 09, 2025 Quick Recommended Links Jobs by Location Job by industries Job Purpose Support the Regulatory Affairs function in its pre-registration and/or post-registration dossier submission activities by assisting in data gathering, screening, collating and compiling of the dossiers, post-registration variations and any other documentation in order to submit the same to the Health Authorities for approval within the defined timelines as per overall objective of Cipla Medpro.
Accountabilities CDT/New dossier submissions and approvals Perform pre-launch activities to ensure timeous submission and registration of products within the defined timelines.
Dossier Life Cycle Management- Perform the dossier life cycle management activities by supporting the post registration variations and other activities to ensure support to the regulatory function and its objectives Support and assist the administrative team in the responsibility to effectively manage and maintain dossiers (electronically and hard copies), collection and delivery of documents, ensure smooth operations and maintain quality standards Develop and manage stakeholder relationships by communicating and interacting on a regular basis in order to achieve the functional objectives Education Qualification BPharm or BSc.
or higher post graduate scientific degree Relevant Work Experience Minimum 2 years of experience in the regulatory function covering all areas, Attention to detail, Resilience, Collaborative approach, time-management, good communication skills, team player; experience in e-CTD submissions Pharmaceutical  jobs