Pharmacovigilance Specialist (m/f/d)

☞ mamgo

View: 147

Update day: 29-03-2024

Location: Lucerne Luzern LU

Category: Executive management Production / Operation

Industry: Technology Information Internet

Position: Entry level

Job type: Full-time

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Job content

My duties
  • Responsible for execution of local PV processes and activities in collaboration with internal functional areas and external parties as assigned
  • Responsible for day-to-day adverse events case management including case intake, tracking, translation to English (as applicable), acknowledgments, and follow-up activities in accordance with PV procedures and country regulations
  • Responsible for reporting adverse experiences or events (AE) or product quality complaints (PQCs) associated with the use of our company products in compliance with Corporate Policy 01: Patient Safety
  • Supports local PV audits and inspections including readiness activities and supports audits of business partners/vendors including the development of CAPAs in response to findings/observations as assigned
  • Participates in compliance activities and coordinates the preparation of necessary corrective actions locally for late reports
  • Supports training of local company staff, distributors, vendors, and business partners as instructed by their manager

My Qualifications
  • Experience in the pharmaceutical industry with a specific focus on safety and pharmacovigilance related activities
  • General knowledge of relevant PV regulations
  • Must be fluent in English and ideally French (written and spoken) while proficient in German
  • Strong communications, organizational, and time management skills
  • Excellent teamplayer and also able to work independently with no supervision
  • Ability to interface broadly with colleagues within related functions and cross-functionally and be able to work independently with no supervision except in the most complex of situations

My Benefits
  • Max commuting time: 2 hours (door to door)
  • A day in the job: At the beginning mainly PV Intake activities (including reconciliation and followup), Individual case safety report (ICSR) and aggregate submissions, compliance monitoring.
  • Hybrid working model with 2 days office days/week (increased office presence will be required during on-boarding phase)

About Hays

With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.

My contact at Hays

Contact

E-Mail: positionen@hays.ch

Tel: +41 44 225 50 00

Reference number

635287/1
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Deadline: 13-05-2024

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