Senior Report Specialist
hace 1 semana
Bayer is a visionary company driven to solve the world's toughest challenges. We're committed to making a real difference in the lives of people around the world. As a Senior Report Specialist, you will play a critical role in supporting our Preclinical Development team in creating, preparing, and processing non-clinical toxicology and DMPK reports for authority submissions.
The team ensures eCTD readiness and compliance with regulatory requirements. You will work closely with a cross-functional group of colleagues within PCD (ED Documentation Group) who prepare and maintain non-clinical reports in the system.
We're looking for someone with excellent technical skills in Document Management systems and the ability to work in a team. The workload varies in terms of time and quantity, so flexibility is required.
Key Responsibilities:
- Technical preparation of non-clinical reports for eCTD readiness in Document Management (DMS)
- Processing and compilation of regulatory submission relevant non-clinical reports in DMS BRAVE
- Excellent skills in Microsoft Office Word, Adobe Acrobat Pro DC, and Document Management System (DMS) BRAVE
- Very good verbal and written English skills, with very good verbal and written German skills a plus
- Basic knowledge of and experience with Good Laboratory Practice (GLP)
What We Offer:
At Bayer, we're passionate about making a difference in the world. We offer a dynamic and supportive work environment, with opportunities for growth and development. If you're looking for a challenging and rewarding role, we encourage you to apply.
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