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Associate Principal Scientist, Engineering

LinkedIn Merck Rahway, NJ
Associate Posted March 31, 2026 Job link
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Requirements
  • Relevant work experience in chemical process development, including the following:
  • Experience to 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
  • 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
  • Familiarity with concepts and application of current Good Manufacturing Practices (cGMPs) ideally during pharmaceutical drug substance / drug product development and production, e.g. in a pilot and/or factory setting
  • Bioprocessing, Chemical Engineering, Chemical Technology, Maintenance Supervision, Manufacturing Process Validation, Manufacturing Scale-Up, Pharmaceutical Industry, Process Characterization, Regulatory Submissions, Small Molecules, Technology Transfer
Preferred Skills
  • 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 (cGMPs) 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.
  • Bioprocessing, Chemical Engineering, Chemical Technology, Maintenance Supervision, Manufacturing Process Validation, Manufacturing Scale-Up, Pharmaceutical Industry, Process Characterization, Regulatory Submissions, Small Molecules, Technology Transfer
Education
  • (Not required) – Education Minimum Requirement:
  • (Not required) – The position requires a 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.