Pharmacovigilance Associate

at  Teva Pharmaceuticals

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Pharmacovigilance Associate
Date: Apr 23, 2024
Location:Jakarta, Indonesia, 13710
Company: Teva Pharmaceuticals
Job Id: 55482

WHO WE ARE

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

THE OPPORTUNITY

We are seeking an experienced Pharmacovigilance (PV) professional to join our dynamic business at Teva. As the Pharmacovigilance Associate, you will be managing the day-to-day operations within the Indonesia PV department. Your key responsibilities include ensuring quality and compliance of all PV deliverables and you will be involved in training, business development, audits/inspections, and the management of the outsourced vendor relationships.
For those currently at Senior PV Associate level, this is a great opportunity for you to step up and lead PV for Indonesia. Additionally, you will have the opportunity to lead and participate in regional PV projects, working with APAC PV team and other global PV departments. At the APAC level, you will also have oversight of all aspects of PV compliance.

YOUR EXPERIENCE AND QUALIFICATIONS

• Bachelor’s Degree in Life Sciences/ Nursing / Pharmacy or related disciplines
• Minimum 3 years of relevant experience within the pharmaceutical industry – ideally in PV, Reg Affairs, Medical Information or Medical Affairs
• Strong understanding and experience in PV at a senior level in the Indonesia market (and other APAC markets, if applicable) and acting as Locally Qualified Person in Indonesia
• Knowledge of ICH guidelines and other global guidelines
• Experience with global safety database
• Strong stakeholder management and communications skills in particular managing and influencing regulators, executives and cross functional leaders
• A self-starter with a hands-on approach and a strong “can-do” attitude, with the ability to work independently and be self-motivated
• Results oriented, and self-motivating with a strong drive to meet and exceed all targets
• Possess a high level of business ethics, integrity, and professionalism

Please refer the Job description for details