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Manufacturing Engineer

Job in Moncks Corner, Berkeley County, South Carolina, 29461, USA
Listing for: MillenniumSoft Inc
Full Time position
Listed on 2026-06-13
Job specializations:
  • Engineering
    Manufacturing Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: Manufacturing Engineer - Urgent Need

Position : Manufacturing Engineer - Urgent Need

Location : Moncks Corner, SC

Duration : 12 Months Contract

Start Time : 8:00 AM

End Time : 5:00 PM

Total Hours/week : 40.00

Mon.

- Fri. 8AM - 5PM

Description

  • Due to exposure to chemicals and latex, screenings must include confirming no eye contacts are allowed in the manufacturing area and that candidates are not allergic to latex.
Purpose
  • Manage and lead process improvement and new product process introduction projects.
  • Coordinate with cross functional teams the design and implementation of new equipment, methods, and processes to enhance the organization's manufacturing capabilities, operational efficiency and effectiveness.
Major Duties And Responsibilities
  • Provide and supervise design engineering services to include but not be limited to: idea conceptualization, investigation of design, machine & tooling design, CAD modeling and detailed component assembly drawings on approved engineering projects as assigned.
  • Provide engineering project management and coordination on various automation & engineering projects as assigned.
  • Evaluation of new types of equipment and methods of manufacturing resulting in recommendations for approval of capital money for such equipment based on economic payback and ROI.
  • Manage system integrator relationships throughout all phases of assigned projects.
  • Develop detailed system requirements definition for automation equipment including detailed listings of all process requirements and acceptance testing.
  • Lead project teams and manage issues and risks within cross functional teams including Quality, Manufacturing, Supply chain, and corporate representatives.
  • Develop an understanding of the current manufacturing processes and identify targets for improvement in transnational and operational efficiencies.
  • Develop and nurture a continuous improvement culture, skill sets, and tools to enhance quality and operational excellence.
  • Develop action plans to achieve short and long-range goals, selection of new production methods.
  • Machine designs, and methods to monitor efficiencies.
  • Develop protocols and coordinate validation of equipment and processes.
  • Develop Standard Operating Procedures (SOPs), work instructions & operating and maintenance procedures supporting manufacturing processes.
  • Maintain knowledge of latest manufacturing methods used in the medical device industry to advance technologies.
  • Participate in defining preventative maintenance programs for production equipment associated with production activities.
  • Ensure information and documentation is consistently accurate and in compliance with regulatory standards.
  • Analyze and plan workforce utilization, space requirements, workflow, and design layout of equipment and work-space for maximum efficiency.
  • Applies statistical methods to estimate future manufacturing requirements and potential.
  • Perform duties in compliance with SOPs and to company quality requirements.
  • May supervise other engineering personnel.
  • Other duties as assigned.
Experience Education Training/Skill Requirements
  • To perform this job successfully, an individual must be able to perform each essential job duty satisfactorily.
  • The requirements listed below are representative of the knowledge, skill, and/or ability required.
  • Bachelor’s Degree in Chemical, Electrical, Mechanical Engineering or related Science.
  • 7+ years of manufacturing process improvement experience.
  • Ability to work independently and effectively with cross-functional teams.
  • Thorough understanding of manufacturing processes and ability to implement ideas.
  • Detail oriented with strong analytical skills.
  • Detailed knowledge of project management planning and execution methods.
  • Detailed knowledge of Medical Device process of validation including IQ, OQ and PQ preferred.
  • Understanding of engineering change management methods and practices.
  • Excellent organizational, troubleshooting, and problem solving skills required.
  • Experience with PLC Controls, robotics, vision systems, data acquisition, system networking and automation Integration preferable.
  • Programming experience preferred.
  • Strong communication skills and ability to communicate effectively with technical and non-technical staff.
  • Experience with MS Office Suite required.
  • Statistical analysis software required. Minitab preferred.
  • CAD experience required. Solid Works preferred.
  • Experience with 3D printing preferred.
Physical Demands And Work Requirements
  • While performing the duties of this job, the employee is frequently required to walk; sit; use hands or arms (to finger, handle or feel objects, tools, or controls).
  • The employee is occasionally required to stand; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl; and talk or hear.
  • The employee must occasionally lift 35 pounds.
  • While performing the duties of this job, the employee frequently works near moving mechanical parts and is frequently exposed to fumes or airborne particles.
  • The employee occasionally works in high places; in outside weather and conditions with toxic or caustic…
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