Key Responsibilities
* Maintain the Pharmacovigilance (PV) Quality Management System to ensure compliance with regulatory PV requirements worldwide.
* Develop and implement training programs for vendors, GPS personnel, and relevant stakeholders on adverse event and product complaint handling.
* Collaborate with subject matter experts to create, review, and update procedures that reflect GPS activities accurately.
* Monitor training compliance and address non-compliance through line management support.
Requirements
* 7+ years of experience in Pharmacovigilance/Drug Safety, Regulatory Affairs, or Quality Assurance within the pharmaceutical/biotech industry.
* Excellent written and verbal communication skills.
* Ability to drive projects independently and prioritize tasks effectively.
* Strong attention to detail and analytical skills.
Working at {company}
{company} values diversity, equity, and inclusion in its workplace. We are committed to equal employment opportunities and will provide reasonable accommodations to qualified individuals with disabilities or chronic illnesses.