Pharmacovigilance Manager
Date: June 3, 2025
Location: Shanghai Shi, China
Company: Teva Pharmaceuticals
Job ID: 62292
Who We Are
We are on a mission to make good health more affordable and accessible, helping millions globally enjoy healthier lives. Our team spans nearly 60 countries with diverse nationalities and backgrounds. As the world’s leading manufacturer of generic medicines and a key producer on the WHO Essential Medicines List, over 200 million people take our medicines daily. We continually seek new ways and people to make a difference.
The Opportunity
Organize and coordinate Pharmacovigilance (PhV) activities across China, Taiwan, and Hong Kong.
Liaise with local markets and key functions (regulatory affairs, medical affairs, supply chain, quality assurance, marketing, legal) to manage and communicate safety-related product information.
Maintain PhV compliance per Teva corporate standards and local regulations.
Oversee adverse event collection and reporting.
Act as the Qualified Person responsible for Pharmacovigilance (QPPV) ensuring compliance with local regulations and standards.
Collaborate cross-functionally to perform risk minimization activities.
How You’ll Spend Your Day
General Pharmacovigilance Tasks:
Serve as QPPV for China, Taiwan, and Hong Kong per local requirements.
Establish, maintain, and oversee the local PhV system.
Act as Local Safety Officer and primary interface with regional PhV team.
Develop and train on local SOPs/WIs for cross-functional communication flows.
Coordinate PhV activities with local distributors and ensure contract compliance.
Align with regional PhV management on business development.
Provide expert input to regional and global PhV management to ensure regulatory adherence.
Support medical affairs and marketing on clinical trials, PMS, market research, and patient support programs by providing PhV input.
Adverse Event Management and Communication:
Manage collection and communication of adverse event reports and safety information.
Ensure timely submission of adverse events to local authorities.
CCSI Handling:
Review updated CCSI and confirm if local Product Information changes are needed.
PSUR Handling:
Confirm PSUR requirements for registered products.
Develop and manage PSUR submission schedules.
Translate/re-format and submit PSURs to national authorities as required.
RMP Handling:
Collaborate on local Risk Management Plans (RMP) with regional teams and local Regulatory Affairs.
Coordinate implementation of RMPs.
Address additional Health Authority requests.
Regulatory Compliance, Audits, and Inspections:
Monitor PhV legislation progress in cooperation with local RA or partners.
Assist with preparation for local audits and inspections.
Manage CAPAs related to audit/inspection findings.
System Management:
Maintain accurate document repositories for agreements, RMPs, PSURs, ICSRs (e.g., Trackwise, Delta).
Your Experience and Qualifications
University degree in life sciences, healthcare, nursing, pharmacy, or related disciplines.
Minimum 3 years relevant experience in a global multinational company; regional experience preferred.
Strong understanding of PhV at a senior level in China and Hong Kong markets; experience as a Locally Qualified Person.
Knowledge of ICH and global guidelines.
Experience with global safety databases.
Make a Difference with Teva Pharmaceuticals
Submit your CV and cover letter addressing key skills and experience related to this role. Only shortlisted candidates will be contacted.
Reports To
Director, Pharmacovigilance
Internal Applicants
Current Teva employees should apply via the internal career site “Employee Central” for priority and exclusive opportunities. Contact HR/IT if you have access issues.
Equal Employment Opportunity Commitment
Teva Pharmaceuticals provides equal employment opportunities without discrimination, committed to diversity and inclusion. Accommodations available throughout recruitment upon request; all information confidential.
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