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Process Engineer

Job in Columbus, Franklin County, Ohio, 43224, USA
Listing for: Intellectt INC
Full Time position
Listed on 2026-09-05
Job specializations:
  • Engineering
    Validation Engineer, Process Engineer, Quality Engineering, Pharma Engineer
  • Pharmaceutical
    Validation Engineer, Quality Engineering, Pharma Engineer
Salary/Wage Range or Industry Benchmark: 40 - 55 USD Hourly USD 40.00 55.00 HOUR
Job Description & How to Apply Below

Title :
Process Engineer

Location:

Columbus, OH | 100% Onsite

Employment Type:

Contract
Duration: 6 12+ Months
Pay Rate : $40-55/hr on W2 ( DOE )

About the Role

We are seeking Process Engineers to support pharmaceutical process scale-up, technology transfer, validation, and commercial manufacturing readiness for small molecule products. The role will work closely with Manufacturing, Quality, Development, and external partners to support product launches and process improvements.

Key Responsibilities
  • Support process validation, technology transfer, and scale-up activities.
  • Provide technical support for commercial manufacturing operations.
  • Develop and update batch records and manufacturing documentation.
  • Support product launches, validation campaigns, and lifecycle initiatives.
  • Identify process risks and develop appropriate mitigation strategies.
  • Troubleshoot manufacturing process issues and drive improvements.
  • Support CAPA, process improvement, and continuous improvement activities.
  • Collaborate with cross-functional teams and external partners.
Required Qualifications
  • Bachelor's degree in Engineering, Chemistry, Pharmacy, or related scientific field.
  • Experience in pharmaceutical process engineering and process validation.
  • Experience with technology transfer, scale-up, manufacturing support, and batch record development.
  • Strong problem-solving, leadership, communication, and collaboration skills.
  • Ability to work independently in a fast-paced manufacturing environment.
Preferred Qualifications
  • Experience with oral solid dosage (OSD) and/or liquid products.
  • Small molecule pharmaceutical manufacturing experience.
  • Experience with Minitab or statistical analysis.
  • Experience supporting commercial launches, CAPA, process improvements, and lifecycle management.
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