The posting
The role develops robust manufacturing processes for parenteral drug products, from process characterization to technology transfer and commercial launch.
## Tasks - Develop manufacturing processes for parenteral liquid and lyophilized formulations - Design and execute process characterization and process design studies - Lead technology transfer projects to global commercial manufacturing sites - Represent process development in cross-functional and international project teams - Collaborate with manufacturing sites to ensure successful project execution - Author sections of regulatory submissions for Phase 1-3 and marketing applications
## Profile - PhD or master's degree in chemistry, chemical or process engineering, or related field - Minimum 5 years of industry experience in drug product process development - Expertise in parenteral process development and technology transfer to commercial sites - Experience designing and justifying down-scale models and process parameters - Track record of parenteral drug product launches for synthetic molecules - Experience authoring drug product sections of regulatory submissions (NDA/BLA) - Willingness to travel internationally up to 20 percent
## Offer - 3–6 months interim, then a permanent position
## Company Pharmaceutical development
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