Senior Regulatory Affairs Manager, Chemistry Manufacturing and Controls

What you’d do

Provides CMC regulatory strategy for development projects and marketed Pharmaceutical Diagnostics products, developing and maintaining the Quality sections (Module 2.3 and Module 3) of product dossiers across the product life cycle. Full time, remote. Found on the employer's careers page on Oct 21, 2026. Apply through the link.

You’ll need

• Bachelor's Degree
• 6+ years of experience
• Experience in diagnostic, pharmaceutical, or medical device industry
• CMC regulatory strategy experience
• Ability to prioritize, plan and evaluate deliverables