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Pharmacovigilance Associate Ii

3-5 years
Not Disclosed
10 June 4, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Pharmacovigilance Associate II

Date: May 21, 2025
Location: Ciudad De Mexico, Mexico, 03810
Company: Teva Pharmaceuticals
Job ID: 61946


Who We Are

We’re on a mission to make good health affordable and accessible, helping millions worldwide live healthier lives. Our team spans nearly 60 countries and diverse backgrounds. As the world’s leading generic medicine manufacturer and a key producer on the WHO Essential Medicines List, over 200 million people take our medicines daily. We’re continually seeking new ways to make an impact and new people to join us.


The Opportunity

  • Perform pharmacovigilance activities within the North America PV unit.

  • Collaborate with Drug Safety Specialists, Pharmacovigilance Safety Specialists, and Managers/Directors.

  • Receive and review adverse event information for pre-marketing and post-marketing products.

  • Liaise with other Teva business units and serve as a resource for the team.

  • Ensure accurate records of all PV activities are created, organized, and maintained according to global/local SOPs and WIs, updating as regulations require.


How You’ll Spend Your Day

  • Receive adverse event information including XML extraction, upload, and receipt.

  • Perform case registration by entering search information.

  • Submit adverse event information to licensed partners within agreed timelines.

  • Collect additional information from reporters and follow up with healthcare professionals and consumers.

  • Review and assess reportability of adverse events to FDA or Health Canada as appropriate.

  • Manage negative acknowledgements from FDA and Health Canada, taking necessary actions.

  • Participate in Pharmacovigilance Quality Management System (QMS) activities.

  • Perform Pharmacovigilance reconciliation tasks.


Your Experience and Qualifications

  • Bachelor of Science in life sciences (pharmacy, physiology, biochemistry, anatomy, pharmacology, microbiology).

  • 3 to 5 years in health or pharmaceutical sectors; minimum 2 years in Pharmacovigilance.

  • Advanced English proficiency.

  • Proficient in MS Word, Excel, PowerPoint, Outlook.

  • Familiarity with PV IT systems such as Veeva Vault, ArisG, Argus, and Cognos is a plus.

  • Comfort with Veeva Vault security database and medical terminology.

  • Knowledge of FDA, Health Canada, and international PV regulations.


Reports To

Senior Manager, Pharmacovigilance


Internal Applicants

Current Teva employees should apply via the internal career site “Employee Central” for priority processing and access to exclusive jobs. Contact local HR/IT for access issues.


Equal Employment Opportunity Commitment

Teva is an equal opportunity employer committed to diversity and inclusion, providing employment without discrimination or bias. Accommodations are available during recruitment and selection as needed.