Full-Time

Associate Principal Scientist

Engineering

Posted on 4/22/2025

Deadline 5/12/25
Inventing for Life

Inventing for Life

Compensation Overview

$139.6k - $219.7k/yr

+ Bonus + Long Term Incentive

Senior, Expert

H1B Sponsorship Available

Linden, NJ, USA

Hybrid work model: 3 days in office, 1 day remote. Candidates must be based in the U.S.

Category
Lab & Research
Interdisciplinary Research
Life Sciences
Required Skills
Data Analysis
Requirements
  • BS and/or MS in Chemical Engineering or a related field from an accredited college/university plus at least 8 years of relevant work experience in process development or PhD with at least 4 years of relevant work experience post PhD defense
  • Demonstrated capability to develop and execute an experimental program to address issues of process design, robustness and productivity
  • Experience with process scale-up and technology transfer, moving from laboratory to pilot plant or factory
  • Ability to mentor technical staff in the laboratory and through data analysis
  • Highly effective communication and collaboration skills
  • Good organizational, interpersonal, writing, and time management skills
  • Ability to operate within a cross-functional process development team
Responsibilities
  • Develop safe and robust manufacturing processes through process characterization, technology transfer, validation, filing and supply support of late-stage projects in the small molecule pipeline
  • Provide scientific expertise by learning and utilizing Quality Risk Management methodologies and tools for statistical design of experiments
  • Conduct hands-on experimentation at the laboratory bench and kilo lab scales
  • Mentor junior staff to initiate, plan and execute characterization and complete technical support objectives
  • Exhibit a mindset of safety and quality compliance, including following current Good Manufacturing Practices (cGMPs), and participating in risk assessments, deviation investigations, and Good Documentation Practices (GDPs)
Desired Qualifications
  • Experience performing lab-based research/process development including performing unit operations common in small molecule drug substance process development such as 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
  • Familiarity with concepts and application of current Good Manufacturing Practices ideally during pharmaceutical drug substance / drug product development and production, e.g. in a pilot and/or factory setting
  • Experience with mathematical modeling, theoretical scaling calculations, and Quality by Design principles.

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INACTIVE