US

Job Search

Refine your search

Deputy EUQPPV (m/w) - Hessen

  • Job type:Permanent
  • Salary:Negotiable
  • Location:Hessen
  • Reference:PR-32599552

Deputy EUQPPV (m/w) - Hessen

Work as "Deputy EUQPPV (m/w)" at a global leader in the plasma protein biotherapeutics industry in Hessen, Germany. The position includes a wide range on responsibilities and provides a lot of variation.

Responsibilities:

  • Support the EU-QPPV in all aspects and take over full EU-QPPV accountability when the EU-QPPV is absent
  • Deputizes for all managerial tasks and responsibilities for the QPPV Office
  • Takes the lead for targeted investigations and improvement initiatives as per delegation by the QPPV
  • Accountable for keeping specific parts of the Pharmacovigilance System Master File up to date and ensure compliance
  • Contribute to and coordinate communications to the Regulatory Authorities relating to safety and pharmacovigilance matters and coordinates responses to any request from Regulatory Authorities for (further) information
  • Critical review of benefit-risk evaluation, aggregate reports and planned RM measures
  • Oversight over PV operations and PV systems such as but not limited to
  • Safety Database and ICSR receipt and reporting
  • Regions
  • PV Agreements
  • PV Quality Management and respective compliance as delegated by the EU-QPPV
  • Supports the EU-QPPV in ensuring global inspection readiness at all PV sites through regular review of the pharmacovigilance system including its quality system and takes a risk- based approach when designing and implementing CAPAs.
  • Closely cooperates with the affiliates and GCSP Regions in order to ensure compliance and inspection readiness
  • Deputizes the EU-QPPV in the Global Safety Governance system, specifically in the Global Safety Review Team (GSRT) and Global Safety Committee (GSC).

Your profile:

  • Medical Doctor with working experience as a physician minimum 3 years working experience in the Pharmacovigilance
  • Excellent knowledge of regulations, particularly EU Significant service within a global Pharmacovigilance function
  • Good knowledge in Risk Management

Advantages:

  • International company
  • Intercultural Team
  • flexible working time
  • Home office
  • attractive salary
  • withinthenextyearsdevelopmenttotheEUQPPV

As a Recruitment Consultant in the area Drug Safety, I would like to give you more information about that vacancy and will assist you in the complete application process.

If you are interested in that vacancy, I look forward to your email with an actual CV and an proposed date for a phone call.

Julia Ecker, T: +49 (0) 89 5519 7711, E: j.ecker(at)prlifesciences.com

Für mehr Informationen über Progressive Recruitment besuchen Sie www.progressive.de

Submit your CV

Update your CV

As part of Progressive Recruitment commitment to supporting you in your career and improving your job prospects we'd like to share industry:

  • news and information
  • recruitment & salary trends
  • reports and whitepapers
  • events and conferences

Please note: we will never sell your data or share it without your express permission

SThree is parent company to the following specialist recruitment businesses:

Real Staffing Group:
Pharmaceuticals. Biotechnology & medical devices sectors
Huxley Associates:
Banking & Finance, Energy & Renewables, Technology and professional services
Computer Futures:
IT
Progressive Global Energy:
Oil & Gas, Mining and Maritime
Progressive:
IT & Engineering

SThree is parent company to the following specialist recruitment businesses:

Real Staffing Group:
Pharmaceuticals. Biotechnology & medical devices sectors
Huxley Associates:
Banking & Finance, Energy & Renewables, Technology and professional services
Computer Futures:
IT
Progressive Global Energy:
Oil & Gas, Mining and Maritime
Progressive:
IT & Engineering