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Process Engineer III

Job in Newark, Essex County, New Jersey, 07175, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-09-08
Job specializations:
  • Engineering
    Process Engineer, Quality Engineering, Manufacturing Engineer, Validation Engineer
Salary/Wage Range or Industry Benchmark: 95000 - 140000 USD Yearly USD 95000.00 140000.00 YEAR
Job Description & How to Apply Below

The primary job function of this position is to provide technical support to cross-functional teams with little or no supervision, applying project management, engineering, and product/process knowledge to complete projects from concept through closure.

Responsibilities:
  • Lead process engineering activities (Process Validation, Cleaning Validation, Equipment Qualification IQ/OQ/PQ, root-cause investigations).
  • Support/monitor Production to troubleshoot material, process, and equipment issues; analyze data using structured techniques, data acquisition, process capability analysis, SPC, and other statistics.
  • Provide technical evaluations for Engineering Change Orders and Supplier Changes (updates to specs/drawings/procedures; operator training).
  • Design/develop equipment and processes for manufacturing; design/build/qualify fixtures, machines, or equipment.
  • Support integration of new products into manufacturing (materials, processing, manufacture, cost inputs).
  • Assist in validation of new/revised processes and equipment to meet standards/specifications.
  • Design and execute engineering studies to test project hypotheses.
  • Apply scientific/technical knowledge for timely execution; may supervise engineers/technicians.
Qualifications:
  • Bachelor's in Engineering/Science (or closely related) desired; or equivalent experience; 5+ years significant engineering/operational experience (post-graduate degree desired).
  • Demonstrated competency; strong technical knowledge and judgment on complex problems.
  • Collaborative communication and interpersonal/negotiation skills.
  • Technical background in medical devices, pharmaceutical, biologics, or similar industries.
  • Demonstrated competency with financial systems and fiscal control.
Preferred:
  • 5+ years Process Engineering in GMP operations;
    Cleaning Validation and Equipment Qualification (IQ/OQ/PQ).
Benefits (if eligible):
  • paid time off (vacation/holidays/sick), medical/dental/vision insurance, 401(k), and eligibility for short-term incentive programs.
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