Job Requirements

Join our team as a PV Intern, for 12 months, reporting to the RA/aPV Country Lead. You’ll gain hands-on experience in the pharmaceutical industry, working closely with a mentor in a dynamic, multidisciplinary environment.

Key Responsibilities:

Collaborate with a mentor to manage adverse event cases and ensure compliance with global and local regulations.Participate in PV activities such as case processing, audits, inspections, and documentation.Complete company training courses and stay updated on local and EU legislation.Support local PV audits, inspections, and develop corrective actions for non-compliance issues.

Tasks:

Manage day-to-day adverse event cases, including intake, follow-up, and reconciliation.Process safety reports and ensure compliance with PV systems and quality management.File and archive safety-related data and documentation.Assist in developing local procedures and improving efficiency.

Competencies and Qualifications:

Qualifications:

Personal: Good time management, organizational, and collaboration skills. Strong communication (verbal and written) and compliance mindset. Self-motivated and proactive.Project Management: Ability to organize, prioritize tasks, and utilize resources effectively.Business Knowledge: General understanding of business trends to optimize activities and improve quality.Regulatory & Compliance: Awareness of Spanish and European regulations, pharmacovigilance concepts, and local SOPs.Computer Skills: Proficient in word processing, presentations, spreadsheets, and learning new systems.Collaboration: Ability to work well with others to achieve quality goals.Communication: Strong oral and written communication skills in English; proficiency in French is a plus.

Requirements:

Post-graduate education in pharmacovigilance, pharmaceutical industry, or related field.Degree in health, life science, or medical science.Fluent in English; local language proficiency is beneficial.