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Manufacturing Engineer, Manufacturing Fill Finish) Night Shift

Job in Holly Springs, Wake County, North Carolina, 27540, USA
Listing for: CSL Vifor
Full Time position
Listed on 2026-09-22
Job specializations:
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering, Validation Engineer, Lean Manufacturing / Six Sigma
Salary/Wage Range or Industry Benchmark: 90000 - 110000 USD Yearly USD 90000.00 110000.00 YEAR
Job Description & How to Apply Below

The incumbent will be a member of theTeam at the Holly Springs Influenza Vaccine manufacturing facility, supporting

Fill/Finish Operations.

The 24/7 Manufacturing Engineering function provides technical support and troubleshooting expertise to manufacturing organizations to achieve supply targets,maximize capacity and maintain equipment uptime.

This position is for a Night Shift Engineer working a 2-2-3 schedule. There are two Engineers on each night shift, plus overlap from the Manufacturing Engineering Manager during the 2-2 evenings of the schedule.

Responsibilities:

  • Providing technicalsupportrelated to the process, equipment, and business systems across all departments within

    Fill/Finish Manufacturing.

    This function acts asfront-line support of production and process-specific issues.
  • Provide support to manufacturing as thefirst lineof contact for technical and operational equipment/process issues. Troubleshoot,investigate and resolvea range of equipment problems in the manufacturing facility, leading the issue resolution effort and coordinating with appropriate teams as needed.
  • Author and improve manufacturing documentation (procedures, batch records, training materials,work instructions, etc.). This function involves revising, creating, and withdrawing documentation.

    This function should also assist with reviews and approvals of documentation.
  • Ownership of quality records including incidents, DCEs, CAPAs, Level 1 and 2 change controls.
  • Support evaluation actions for related change controls.
  • Assist with investigations related to product and process including complaints,deviations, or adverse process trends withinthe Bulk or Fill/Finish Manufacturing.
  • Support process improvement projects toensure safe and efficient operations.

Requirements:

  • Bachelor’s degree in an engineering or science discipline or equivalent experience in pharmaceutical, manufacturing, or equivalent industry preferred.

Minimum 1 year of related industry experience required in the pharmaceutical/biotech industry

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