Expert In Drug Product Formulation And Processing For Synthetic Molecule Parenterals (cmc Advisor)
Roche UK
Basel, Switzerland
Parenteral drug product development
Peptide formulation and process development
Nda authoring for peptide products
The Pharmaceutical Development DP SM Parenterals group is responsible for the development of parenteral drug products Synthetic molecules from Phase 1 through Launch
Job Summary
The Pharmaceutical Development DP SM Parenterals group is responsible for the development of parenteral drug products Synthetic molecules from Phase 1 through Launch.
The position requires deep scientific expertise and strategic vision to support the drug development portfolio (CMC expertise) and drive innovation within cross-functional teams.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
Matching Summary
The Pharmaceutical Development DP SM Parenterals group is responsible for the development of parenteral drug products Synthetic molecules from Phase 1 through Launch.
Skills & Requirements
Must-have
Parenteral drug product development
Peptide formulation and process development
NDA authoring for peptide products
Aseptic manufacturing processes
Regulatory CMC document authoring
Nice-to-have
Strategic vision and innovation
Cross-functional team leadership
Mentoring and coaching staff
Open dialogue and genuine connections
Problem-solving mindset and passion for innovation