Responsibilities
- Invent synthetic routes and develop safe, robust, and cost-effective processes to manufacture synthetic and hybrid drug substances.
- Advance enabling technologies to accelerate pharmaceutical development and to improve sustainability and process efficiency.
- Support cGMP manufacturing and technology transfer to our internal manufacturing facilities and external contract manufacturers.
- Ensure process performance through process understanding, modeling and characterization.
- Contribute to drug substance development teams by providing experimental results, technical updates, documentation, data interpretation, recommendations, etc.
- Work cross-functionally to deliver regulatory documents and support regulatory filings.
- Serve as a technical expert and keep current in the field of organic and process chemistry.
- Work effectively in a multi-disciplinary team of chemists, engineers and attribute scientists.
- Work independently in advancing projects and studies within required deadlines.
Requirements
- Doctorate degree PhD OR PharmD OR MD Chemistry completed by August 2026 OR Master’s degree and 3 years of Scientific experience OR Bachelor’s degree and 5 years of Scientific experience
- Ph.D. in organic chemistry with a specialization in total synthesis, reaction methodology, mechanistic studies
- Post-doctoral experience in an academic laboratory or pharmaceutical/biotech industry
- Track record of peer-reviewed publications and research presentations
- Demonstrated ability to work within a dynamic and interdisciplinary environment to achieve results
- Excellent written and verbal communication skills, ability to multitask, effectively plan and follow through on complex projects
Core Competencies
Demonstrates expertise in organic chemistry, particularly in total synthesis and reaction methodology, while effectively collaborating in interdisciplinary teams to advance pharmaceutical development and ensure compliance with cGMP standards.
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