Sr. PV Scientist, Quality Document

Play a key role in reviewing and improving pharmacovigilance documentation within a leading biotech company.

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. 

Role: Senior Pharmacovigilance Scientist, Quality Document Manager

Location: Baar, Switzerland

Start: ASAP

Duration: 12 months with possible extension

Workload: 100% 

• 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. 

• 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.