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Senior Manager (M/F/D) Pharmacovigilance 100%

5+ years
Not Disclosed
10 Jan. 3, 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

Senior Manager (m/f/d) Pharmacovigilance
Location: Basel, Switzerland
Full-time: 100%

Teva Pharmaceuticals, a leading global supplier of generics, is seeking an experienced Senior Manager for Pharmacovigilance to join our team in Basel. In this role, you will serve as the Local Safety Officer (LSO) and Qualified Person for Pharmacovigilance (QPPV) for Switzerland and Liechtenstein, overseeing pharmacovigilance tasks and ensuring compliance with local regulations.


Key Responsibilities:

  • Routine Pharmacovigilance Tasks:
    • Oversee case processing (collection, global database entry, QC, follow-up, and submission).
    • Collaborate with Regulatory Affairs on PSURs, RMPs, CCSI, and signal management.
    • Develop and implement pharmacovigilance and risk minimization activities for Teva and Mepha’s products in Switzerland.
    • Maintain local pharmacovigilance agreements and coordinate Health Hazard Assessments.
    • Ensure compliance with Swiss regulations and internal SOPs, including for external partners.
    • Act as the main point of contact for Swissmedic on all pharmacovigilance matters.
  • PV DACH Cluster Topics:
    • Lead and execute pharmacovigilance activities for DACH (Germany, Austria, Switzerland) countries.
    • Work closely with local LSOs and Teva Global to ensure regulatory compliance.
    • Provide backup for LSO-Austria and LSO-Germany.
  • Leadership & Collaboration:
    • Lead the local Pharmacovigilance team, with budget responsibility.
    • Represent pharmacovigilance in local projects and activities.
    • Foster strong working relationships with interfacing units and external partners.
    • Contribute to association work within pharmacovigilance.

Your Qualifications:

  • Education: Master’s degree in Life Sciences, Pharmacy, or a related field.
  • Experience: At least 5 years of experience in pharmacovigilance, preferably within the Swiss pharmaceutical industry.
  • Knowledge: In-depth understanding of Swiss pharmacovigilance regulations, ICH (GCP), EU GVP, and medical knowledge.
  • Languages: Fluent in English and German. Proficiency in Italian and/or French is a plus.
  • Leadership: Experience in leading teams is preferred.
  • Technical Skills: Proficiency in Microsoft Office tools (Excel, Word, PowerPoint).
  • Soft Skills: Strong communication skills, ability to manage multitasking, and work within a matrix organization.

What We Offer:

  • Dynamic Role: Engage in a varied and exciting role within a growing, international organization.
  • Challenging Work: Gain valuable insights into various business processes and contribute to regulatory compliance and safety.
  • Perks: Lunch card, public transport allowance, and a central office location with easy access to Basel SBB train station.
  • Work Environment: A collaborative and inclusive team focused on growth and professional development.

Teva Pharmaceuticals is committed to Equal Employment Opportunity and values a diverse and inclusive workforce. If you require any accommodations throughout the recruitment process, please contact us for assistance.


Contact:
Kamila Walawska, Human Resources

Teva is dedicated to creating an accessible candidate experience. If you're a current Teva employee, please apply using the internal career site available on Employee Central.