Pharmacovigilance Specialist

Are you passionate about drug safety, compliance, and improving patient wellbeing? Join an international pharmaceutical organization as a Pharmacovigilance Specialist and help ensure medicines are monitored and managed safely throughout their lifecycle.

As a Pharmacovigilance Specialist, you will support local pharmacovigilance and drug safety activities, ensuring compliance with regulatory requirements and company procedures. You will play an important role in monitoring product safety, managing regulatory documentation, and supporting audits and inspections.

Key responsibilities:

• Managing and coordinating adverse event and drug safety reporting activities;
• Supporting pharmacovigilance compliance in line with local and global regulations;
• Maintaining accurate safety documentation, records, and procedures;
• Supporting regulatory inspections, audits, and follow-up actions;
• Coordinating with internal teams, external partners, and health authorities;
• Monitoring changes in pharmacovigilance regulations and implementing updates;
• Supporting risk management activities and safety-related projects;
• Providing guidance and training on pharmacovigilance processes and requirements;
• Ensuring timely and accurate communication with relevant stakeholders;
• Contributing to continuous improvement of local safety and compliance processes.

• Salary of €6,700 gross per month;
• Full-time position of 40 hours per week in Haarlem;
• Contract until November 2027 (maternity leave replacement);
• Hybrid working environment with 2 office days per week;
• Paid vacation days and 8.33% holiday allowance;
• Pension plan from the first day of employment;
• Access to training and development opportunities through Adecco Academy;
• Opportunity to work in a leading international pharmaceutical organization;
• A role with a high level of responsibility and impact on patient safety.

You will join an international pharmaceutical company focused on delivering safe and effective healthcare solutions. You will work closely with Regulatory Affairs, Medical Affairs, Quality, and Pharmacovigilance teams, contributing to patient safety and regulatory excellence across the business.

• Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or a related field;
• Experience in Pharmacovigilance, Drug Safety, Regulatory Affairs, or a similar pharmaceutical role;
• Knowledge of adverse event reporting and pharmacovigilance regulations;
• Experience supporting audits, inspections, or compliance activities is preferred;
• Professional level of English and Dutch, both written and spoken;
• Strong attention to detail and documentation skills;
• Strong communication and stakeholder management skills;
• Proactive, organized, and quality-focused mindset.

Do you have experience in pharmacovigilance or drug safety and want to contribute to patient safety in a global environment? Apply now and become part of a team dedicated to maintaining the highest standards of regulatory compliance and healthcare quality. We look forward to receiving your application.