About the Role Our client is seeking a diligent and experienced Pharmacovigilance Specialist to join their dedicated safety team in Paarl . This role is essential for monitoring the safety of our client's pharmaceutical products post-market, ensuring compliance with global regulatory requirements, and protecting patient health. You will be responsible for collecting, assessing, and reporting adverse events, as well as contributing to signal detection and risk management activities. This is a critical position within the pharmaceutical industry , offering the chance to contribute significantly to drug safety and public health. Key Responsibilities Collect, process, and document adverse event reports from various sources. Assess seriousness and causality of adverse events according to company and regulatory standards. Prepare and submit regulatory safety reports within strict timelines. Support signal detection activities and contribute to risk management plans. Maintain the pharmacovigilance database and ensure data accuracy and completeness. Collaborate with internal stakeholders (e.g., Medical, Regulatory) and external partners on safety matters. Requirements Bachelor's degree in Pharmacy, Nursing, Life Sciences, or a related healthcare field. Minimum of 3 years of experience in pharmacovigilance or drug safety. Solid understanding of global pharmacovigilance regulations and reporting requirements (e.g., ICH E2A, E2B). Experience with safety databases and adverse event reporting systems. Strong analytical and critical thinking skills with excellent attention to detail. Proficiency in English, with excellent written and verbal communication skills. Benefits Competitive annual salary and potential for bonuses. Comprehensive medical and retirement benefits. Opportunities for specialized training in pharmacovigilance and drug safety. A collaborative and supportive work environment. Contribution to ensuring the safety of pharmaceutical products. #J-18808-Ljbffr
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