About this role
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.
What are you going to do? 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.
- What do we offer?- 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.
Where will you work?
You will join an international p