Zoetis

Pharmacovigilance Medical Manager – Deputy Qualified Person Responsible for Pharmacovigilance

Zoetis

full-time

Posted on:

Location Type: Remote

Location: Germany

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About the role

  • Good understanding of the ADE reporting regulations (US and EU) and of product trending standards.
  • Collaborate with signal management team regarding validation activities for assigned products (including signal detection) to comply with FDA/USDA/EU expectations and to better understand the safety and efficacy profiles of Zoetis products post-marketing.
  • Prepare trending reports of assigned marketed products to the pharmacovigilance stakeholders and make recommendations regarding potential safety and efficacy profile adjustments.
  • Provide input for negotiations with regulatory agencies regarding submission of ADE reports as well as for responses to these agencies about product safety and efficacy issues.
  • Assist in the design pharmacovigilance policies as needed.
  • Assist in the maintenance of a pharmacovigilance electronic system from a data capture, trend analysis and regulatory submission perspective as necessary.
  • Function as Pharmacovigilance subject matter expert for assigned product group(s).
  • Provide pharmacovigilance input for advertising and promotional material upon request.
  • Risk Mitigation in support of Global Manufacturing and Quality and Regulatory label defense activities.
  • Complete pharmacovigilance data requests and Health Hazard Assessments for assigned products upon request.
  • Act as Deputy EU/UK QPPV

Requirements

  • Minimum requirement of a Veterinary Medicine (DVM, VMD)
  • 5 or more years of experience in Veterinary Pharmaceutical Industry including veterinary pharmacovigilance in the European Union.
  • Graduate degree or diploma in animal science and/or epidemiology or related experience is a plus.
  • Ability to review and analyze pharmacovigilance data to develop trending reports is essential.
  • Knowledge of the FDA/USDA and international regulations on Adverse Drug Event (ADE) reporting is a benefit.
  • Strong interpersonal skills, ability to work under pressure and in a highly matrix environment is essential.
  • Experience with database software and pharmacovigilance systems is desirable.
  • May lead/mentor others.
Benefits
  • Attractive remuneration & comprehensive social benefits: A fair, competitive salary plus additional benefits for your security and future.
  • Flexible working & remote model: Enjoy the freedom of flexible working hours with a 37.5-hour week and a possibility to work from a home office.
  • Time to relax: With 30 days of holiday per year, you have plenty of opportunity to switch off and recharge your batteries.
  • Career & further development opportunities: Customized training, workshops and individual career planning for your personal and professional development.
  • Together for a good cause: One paid volunteer day per year so you can get involved in social causes.
  • Mobility that suits you: Benefit from excellent public transport connections as well as our mobility offers such as a company ticket and job bike.
  • Discounts & health offers: Access to numerous employee discounts and a Wellhub membership for fitness and wellness.
  • Focus on mental health: confidential and free counselling for you and your loved ones from the Fürstenberg Institute.
  • Motivating team & inspiring environment: Work in a committed, dynamic team that grows and inspires together.
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
pharmacovigilancedata analysistrending reportsrisk mitigationsignal detectionregulatory submissionHealth Hazard AssessmentsADE reportingveterinary pharmacovigilanceanimal science
Soft Skills
interpersonal skillsability to work under pressurementoringcollaborationcommunicationproblem-solvingorganizational skillsleadershipadaptabilityattention to detail
Certifications
DVMVMDgraduate degree in animal sciencediploma in epidemiology