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together, we’re on a mission to make good health more affordable and accessible, helping millions around the world enjoy healthier lives. Our work spans nearly 60 countries, embracing diverse nationalities and backgrounds. Working here means collaborating with the world’s leading manufacturer of generic medicines, many of which are on the who’s essential medicines list. Currently, over 200 million people worldwide take our medicines daily. We are committed to making a difference and welcoming new talent to join us in this mission.
the opportunity
- be a core member of the safety team, responsible for pharmacovigilance activities within the north american pv unit, collaborating with drug safety specialists and managers to review adverse event data for pre- and post-market products.
- serve as a liaison with other teva business units and as a resource to the team.
- ensure all pv activities are documented, organized, and maintained in compliance with global and local sops, wis, and regulations.
how you’ll spend your day
- assist in preparing risk management plans and associated strategies as per health canada requirements.
- handle local labeling updates and safety variation submissions for teva medicinal products, considering regulatory timelines.
- review and submit psurs and asrs to health canada according to regulations.
- oversee adr reports from the health canada vigilance database to ensure compliance.
- assist in health hazard assessments as needed.
- draft pharmacovigilance agendas and minutes, and archive documents accurately.
- participate in audits and inspections, contribute to process improvements, and support capa reviews.
- complete required training and sop/wi reviews timely.
- update sops/wis when processes change to ensure compliance and efficiency.
- support training of new pv team members on systems and processes.
- engage in local pv activities, manage cases and workflows, and coordinate with other departments.
- lead regional projects as assigned and perform any additional activities assigned by the manager.
your experience and qualifications
education: bachelor’s degree in physics, chemistry, biology, biochemistry, microbiology, physiology, anatomy, or pharmacology.
experience: at least 5 years in healthcare or pharmaceutical industry, with a minimum of 3 years in pharmacovigilance. Proficiency in microsoft office, familiarity with pv it systems like arisg, argus, cognos, and knowledge of fda/health canada regulations are required.
reports to
associate director, canadian local safety officer – pv canada
already working @teva?
if you are a current teva employee, please apply via the internal career site on 'employee central' for priority processing and access to exclusive opportunities. Use the provided link or access from your home network. Contact hr/it if you face issues.
teva’s equal employment opportunity commitment
teva is dedicated to providing equal employment opportunities regardless of age, race, gender, disability, or other protected status. We promote diversity and inclusivity. Please inform us of any accommodations needed during the recruitment process; all information will be kept confidential.
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