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Manufacturing Engineer II

Job in Greenville, Greenville County, South Carolina, 29610, USA
Listing for: International Vitamin Corporation
Full Time position
Listed on 2026-01-27
Job specializations:
  • Engineering
    Manufacturing Engineer, Process Engineer, Automation Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

2 days ago Be among the first 25 applicants

Position Overview

The Manufacturing Engineer II provides engineering expertise in the execution of capital projects. On these projects, you will develop and ensure compliance with capital budgets; develop RFPs and equipment specifications; and perform equipment design review, FAT’s, commissioning, and start‑up applicable to GMP processing equipment. You will interface with external Architecture & Engineering, construction, and equipment vendors as well as internal site project teams in the execution of strategic projects.

You will be responsible for the development of new innovative solutions, identification cost savings opportunities; and provide support to the maintenance teams to troubleshoot equipment problems. This position will be located in AND, DDR, or WOD locations with direct responsibility for the engineering of manufacturing and/or packaging processes in those locations.

Specific Responsibilities
  • Lead the design, integration, installation, and start‑up of capital projects, including estimation, justification, budget, schedule, acquisition, troubleshooting, and documentation.
  • Develop User Requirements Specifications, equipment design specifications.
  • Lead communications with vendors (OEM’s) and contractors to implement “cutting edge” process and automation solutions.
  • Perform Vendor bid analyses and Review/Approve Vendor Documentation.
  • Lead Factory Acceptance Test, Commissioning and Start‑up Activities for your projects.
  • Assisting in the validation / qualification of new systems and equipment.
  • Ensure that all specifications, drawings, and ancillary documents are up to date and accurately filed in master data systems.
  • Work with production, maintenance, and quality to ensure that PM’s, Spare parts, SOPs and other cGMP related documentation are up to date with the latest project installations.
  • Serve as a company subject matter expert (SME), maintaining the latest knowledge of bulk formulation equipment technologies, packaging equipment and concepts to support business growth.
  • Provide engineering solutions for continuous improvement objectives using industry standard tools and procedures (Change Control, ROI, etc).
  • Identify and specify required tooling to meet production requirements.
  • Research and evaluate new company suppliers, processes and equipment.
  • Provide support to maintenance by troubleshooting issues as they arise.

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