Pharmacovigilance Quality Assurance Specialist

hace 1 día


Sant Cugat, Barcelona, España Grifols A tiempo completo
About Grifols

Grifols is a global healthcare company dedicated to improving the health and well-being of people around the world. With a rich history dating back to 1909, we have established ourselves as leaders in plasma-derived medicines and transfusion medicine.

Job Summary

We are seeking a highly skilled Pharmacovigilance QA Specialist to join our Clinical Quality Assurance team. As a key member of our team, you will play a crucial role in ensuring compliance with good pharmacovigilance practices (GVP) and supporting the development of innovative medicines.

Responsibilities
  • Conduct audits according to established plans to ensure compliance with GVP.
  • Collaborate with Global Pharmacovigilance (GPV) staff to resolve audit findings and provide suggestions for improvement.
  • Analyze deviations and CAPAs Management.
  • Support Pharmacovigilance staff regarding compliance issues within the area of expertise.
  • Contribute to the development of training plans and review of SOPs and documentation generated by GPV.
Requirements
  • Bachelor's degree in Health Sciences, with specialization in pharmacovigilance and/or audits being a plus.
  • 3-5 years of experience in pharmacovigilance and/or audits within a pharmaceutical company.
  • Advanced English proficiency (C1.1).
  • Proactive, team player with strong written and oral communication skills.
  • Rigorous and analytical.
About the Role

This is an exciting opportunity to join a dynamic team and contribute to the development of innovative medicines. As a Pharmacovigilance QA Specialist, you will have the chance to work with a global team and make a meaningful impact on the healthcare industry.

What We Offer

Grifols is committed to maintaining an excellent working environment that encourages employee growth and development. We offer a competitive compensation package and opportunities for professional advancement.



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