Sr. PV Scientist, Quality Document

Sr. PV Scientist, Quality Document
Play a key role in reviewing and improving pharmacovigilance documentation within a leading biotech company.
Sr. PV Scientist, Quality Document
Job description:
Our client, a global biotechnology company, is looking for a Senior Pharmacovigilance Scientist, Quality Document Manager to support high\-quality pharmacovigilance documentation and quality processes within the Safety Surveillance \& Aggregate Reports team. This is an excellent opportunity for someone with strong medical writing and pharmacovigilance experience who enjoys working in a collaborative, quality\-focused environment.
About the customer:
Role: Senior Pharmacovigilance Scientist, Quality Document Manager
Location: Baar, Switzerland
Start: ASAP
Duration: 12 months with possible extension
Workload: 100%
Requirements:
Perform quality control reviews of pharmacovigilance and aggregate safety documents, ensuring accuracy, consistency, and compliance.
Verify source data, review scientific and technical content, and provide detailed feedback to document authors.
Support vendor oversight, training, process improvements, template development, and quality documentation initiatives.
Contribute to quality trend reporting, SharePoint maintenance, and other Safety Surveillance support activities.
Competences:
Bachelor's degree in Life Sciences, Natural Sciences, Healthcare, or a related field.
Previous experience in pharmacovigilance, medical writing, scientific editing, or a similar role within the pharmaceutical or biotechnology industry.
Strong understanding of pharmacovigilance, clinical trial safety, post\-marketing safety regulations, and medical terminology.
Excellent written English with exceptional attention to detail and strong document review skills.
Proficient in Microsoft Office (Word, Excel, PowerPoint) and comfortable working with cross\-functional teams. jpid0dd3279jm jit0728jm jiy26jm