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Mgr Pharmacovigilance - 6585

Date: May 20, 2021

Location: Beijing, CN, 00000

Company: Teva Pharmaceuticals

Company Info

Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Job Description

  • Organize and coordinate Pharmacovigilance (PhV) activities in China and Hong Kong.  Liaise with local markets and key functions (regulatory affairs, medical affairs, supply chain, quality assurance, marketing and legal) to make sure safety related information to company products is appropriately managed and communicated. Maintain PhV compliance, as per Teva corporate standards and applicable local regulations and to keep oversight on collection and reporting of adverse events and other safety related reports.
  • Additionally, acting as the Qualified Person, you will need to ensure compliance with the local regulations and standards pertaining to PhV, communication of product safety information, preforming risk minimisation activities in business collaboration and working with cross-functional departments, such as Medical, Regulatory Affairs, Legal and Quality.


  1. University Degree qualification (life sciences) or related disciplines in natural/science/health care or nursing/pharmacy degree

  2. Minimum 3 years of relevant experience, in a global multi-national company - Some regional experience will be advantageous

  3. Strong understanding and experience in PhV at a senior level in the China and Hong Kong market and acting as Locally Qualified Person

  4. Knowledge of ICH guidelines and other global guidelines

  5. Experience with global safety database


Regulatory Affairs

Sub Function


Reports To

In process of validation

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Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.