Regulatory Program Specialist
Roche(1 month ago)
About this role
The Regulatory Program Specialist supports global planning, tracking, and monitoring of regulatory information for pharmaceutical submissions within the Pharma Technical Regulatory Submission Management Group. The role coordinates document flow, ensures version control, and helps deliver timely, compliant submission content in collaboration with cross-functional teams. It contributes to maintaining high-quality regulatory documentation and effective submission execution.
Required Skills
- Word
- Excel
- Acrobat
- SharePoint
- Document Management
- Document Formatting
- Version Control
- Regulatory Submissions
- Attention To Detail
- Time Management
+2 more
Qualifications
- BA or BS in Biology, Chemistry, Pharmacy or Equivalent
About Roche
roche.comAs a pioneer in healthcare, we have been committed to improving lives since the company was founded in 1896 in Basel, Switzerland. Today, Roche creates innovative medicines and diagnostic tests that help millions of patients globally.
View more jobs at Roche →Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at Roche
Similar Jobs
Submission Content Manager, Regulatory Affairs Operations
Olema Oncology(11 days ago)
Associate - Regulatory Affairs (Publishing)
ClinChoice(6 days ago)
Regulatory Publishing Specialist- Veeva Experience Required
Clinical Careers Page(1 month ago)
Regulatory Publishing Specialist (eCTD )
Clinical Careers Page(1 month ago)
Technical Communication Specialist/Coordinator
Oklo(2 months ago)
Senior Clinical Research Associate II
American Association of Physicists in Medicine(1 month ago)