Senior Scientist, Molecule Chemical Engineering
Listed on 2026-06-30
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Engineering
Process Engineer, Chemical Engineer
The Chemical Commercialization Technology (CCT) department, which is part of our Manufacturing Division, is seeking a self‑motivated individual for a Senior Scientist, Engineering role. The position involves developing safe and robust manufacturing processes through process characterization, technology transfer, validation, filing, and supply support of late‑stage projects in the small molecule pipeline.
The scientist will apply Quality Risk Management methodologies, tools for statistical design of experiments, and conduct hands‑on experimentation at laboratory bench and kilo‑lab scales. The role requires a mindset of safety and quality compliance, including following current Good Manufacturing Practices (cGMPs), participating in risk assessments, deviation investigations, and Good Documentation Practices (GDPs).
Education Minimum RequirementThe position requires a BS and/or MS with a minimum of 5 years of relevant work experience or a PhD in Chemical Engineering from an accredited college/university.
Required Experience and Skills- Relevant work experience in chemical process development, including the following:
- Demonstrated capability to develop and execute an experimental program to address issues of process design, robustness, and productivity.
- Highly effective communication and collaboration skills.
- Good organizational, interpersonal, writing, and time‑management skills.
- Ability to operate within a cross‑functional process development team.
- Experience performing lab‑based research/process development including unit operations common in small molecule drug substance development (chemical reactions, work‑up, and crystallization).
- Experience leading regulatory file authoring, validation planning, and execution.
- Experience guiding internal/external technical discussions.
- Familiarity with statistical design and analysis tools.
- Experience with process scale‑up and technology transfer from laboratory to pilot plant or factory.
- Familiarity with current Good Manufacturing Practices (cGMPs) in pharmaceutical drug substance or drug product development, e.g., in a pilot and/or factory setting.
- Experience with mathematical modeling, theoretical scaling calculations, and Quality by Design principles.
- cGMP Regulations
- Chemical Engineering
- Chemical Manufacturing
- Chemical Processes
- Chromatographic Techniques
- Design of Experiments (DOE)
- Process Characterization
- Process Scale Up
- Reaction Engineering
- Small Molecule Synthesis
- Technology Transfer
- Current Employees apply.
- Current Contingent Workers apply.
US and Puerto Rico Residents Only.
BenefitsSalary range: $ – $. The successful candidate will be eligible for an annual bonus and long‑term incentive, if applicable. The company offers a comprehensive benefits package, including medical, dental, vision, other insurance for employees and families, retirement benefits with a 401(k) plan, paid holidays, vacation days, and compassionate and sick days.
EEO StatementAs an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.
For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit the EEOC.
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