Quality Assurance R&d Pharmacovigilance Specialist

Recordati Industria Chimica e Farmaceutica S.p.A

Milano, Italy
On-site
Quality management system
Pharmacovigilance
Good pharmacovigilance practice
The primary objective of this function is to assure the development, implementation, and maintenance of Recordati's Quality Management System in relation to Pharmacovigilance, in alignment with Group and R&D quality standards

Job Summary

  • The primary objective of this function is to assure the development, implementation, and maintenance of Recordati's Quality Management System in relation to Pharmacovigilance, in alignment with Group and R&D quality standards.
  • Responsibilities include coordinating the activities of Affiliates’ QA R&D for Pharmacovigilance and liaising with local QA teams.
  • The role involves interaction with pharmacovigilance personnel at Headquarters, the PV contact person at each SPC Affiliate, and RRD PV personnel as required.

Matching Summary

The primary objective of this function is to assure the development, implementation, and maintenance of Recordati's Quality Management System in relation to Pharmacovigilance, in alignment with Group and R&D quality standards.

Skills & Requirements

Must-have

  • Quality Management System
  • Pharmacovigilance
  • Good Pharmacovigilance Practice
  • SOPs/WIs on PV processes
  • Deviations, CAPA, Change
  • Audit management

Nice-to-have

  • Ability to work across cultures
  • Flexible and adaptable
  • Initiatives and self-motivation capacities
  • Positive thinking and enthusiasm
  • Positive attitude and ability to interact diplomatically

Key Requirements

  • 6-8 years experience in Pharmaceutical companies
  • Project Management
  • Computer System Validation knowledge
  • Knowledge of QA Standards
  • Management / Leadership skills

Work Rights

Not specified

Tailored Resume

Cover Letter