Principal Engineer I, Process Development
$124,500–$236,500 year
On-siteNorth Chicago, Illinois, United States
Job Summary
Lead cross-functional teams to deliver robust processes for late-stage small molecule solid dosage assets and commercial products by solving complex engineering challenges. Conceptualize novel approaches using engineering principles, design experiments to test hypotheses, and extract full relevance from scientific observations. Champion new technologies by implementing technical alternatives derived from literature and industry knowledge, while mentoring colleagues and advising management. Author technical reports and regulatory submissions, consistently present complex data to diverse groups, and maintain broad internal and external contacts to support strategic needs. Ensure compliance with all corporate policies and procedures.
Required Qualifications
- Bachelors, Masters, or PhD in Chemical Engineering, Mechanical Engineering, Bioengineering, Pharmaceutical Sciences, or related field
- 14+ (Bachelors), 12+ (Masters), or 6+ (PhD) years of related work experience
- strong engineering background
- Deep technical background in pharmaceutical development
- Must be very experienced in the lab as well as in the production environment
- Solid oral dosage process development experience
- Must be available for weekend shifts
- Valid driver's license
Desired Qualifications
- Solid oral dosage process development experience is highly preferred
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