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Packaging Engineer

Job in Columbus, Franklin County, Ohio, 43224, USA
Listing for: Intellectt Inc
Full Time position
Listed on 2026-05-22
Job specializations:
  • Manufacturing / Production
    Packaging Engineer, Manufacturing Engineer, Validation Engineer
  • Engineering
    Packaging Engineer, Manufacturing Engineer, Process Engineer, Validation Engineer
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

We are supporting a long-term onsite opportunity with a leading biopharma manufacturing team in Columbus, Ohio for a Sr. C&Q Packaging Equipment Engineer. This role will support the commissioning, qualification, and startup of new automated assembly, labeling, and packaging lines currently in the FAT phase, with installation and qualification activities scheduled next.

The team is seeking a hands‑on engineer with strong equipment qualification experience, particularly in executing IQ/OQ/PQ activities within GMP‑regulated manufacturing environments. While packaging equipment experience is preferred, the hiring manager is primarily focused on candidates who can independently drive commissioning and qualification activities, support startup operations, troubleshoot equipment issues, and complete documentation in a compliant and timely manner.

Key Responsibilities
  • Support commissioning, startup, and qualification activities for automated packaging and assembly equipment
  • Develop and execute IQ/OQ/PQ protocols and validation documentation
  • Perform FAT/SAT support, equipment shakedown, and startup troubleshooting
  • Manage deviations, change controls, CAPAs, traceability matrices, and summary reports
  • Collaborate cross‑functionally with Manufacturing, QA, Automation, Maintenance, vendors, and system integrators
  • Ensure compliance with GMP, FDA, and internal quality standards
Required Qualifications
  • 3+ years of C&Q, validation, or equipment qualification experience in pharma, biotech, medical device, or GMP manufacturing environments
  • Strong experience executing IQ/OQ/PQ protocols for manufacturing or packaging equipment
  • Hands‑on experience with automated equipment such as packaging lines, labeling systems, cartoners, serialization equipment, inspection systems, case packers, or assembly equipment
  • Experience with FAT/SAT, commissioning, startup support, and equipment troubleshooting
  • Strong understanding of GMP documentation practices and regulated environments
  • Excellent communication and cross‑functional coordination skills
Preferred Experience
  • Biopharma or pharmaceutical packaging operations
  • Automated packaging or serialization systems
  • Experience supporting large-scale equipment installation or production line startup projects
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