Senior Engineer in Pharmaceutical Commercialization Technology focused on small molecule solid dosage process development. Objectives Advance drug product manufacturing from pilot to commercial scale, ensuring process robustness and regulatory compliance.
Responsibilities: Plan and interpret process development studies Lead or participate in cross-functional drug product teams Apply QbD principles and process modeling Author technical documents Evaluate new technologies Support innovation initiatives
Qualifications: Bachelor's degree with 6+ years, master’s with 4+ years, or PhD in Chemical/Biochemical Engineering, Materials Science, or Pharmaceutical Sciences Hands-on experience with scale-up, technology transfer, and GxP practices Strong collaboration and communication skills
Preferred Skills: Familiarity with cGMP, NDA/WMA CMC documentation, statistical process control, process modeling, and experience supporting supply chain activities High-Value Small molecule solid dosage development Process validation Commercial scale manufacturing Cross-site collaboration (US, Ireland, Singapore) 25% travel Hybrid work setup in Rahway, NJ

Also on the board Same function, level within a rung

Level

Senior

Location

New York, NY

Occupation

Chemical Engineers

Industry

Pharmaceutical Preparation Manufacturing

Posted

yesterday

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