Manufacturing Engineer assists in planning and designing manufacturing processes for a production facility. Maximizes efficiency by analyzing layout of equipment, workflow, assembly methods, and work force utilization. Being a Manufacturing Engineer determines the parts, equipment, and tools needed in order to achieve manufacturing goals according to product specifications. Requires a bachelor's degree of engineering. Additionally, Manufacturing Engineer typically reports to a supervisor or manager. The Manufacturing Engineer works on projects/matters of limited complexity in a support role. Work is closely managed. To be a Manufacturing Engineer typically requires 0-2 years of related experience. (Copyright 2024 Salary.com)
Hello All,
Greetings from Tanisha Systems !
We are looking for an Manufacturing Engineer at North Haven, CT / Grand Rapids, MI(Onsite ). Find the below JD and if you feel interested in this opportunity then kindly share me your most updated resume at piyush.singh@tanishasystems.com.
Position : Manufacturing Engineer
Location : North Haven, CT/ Grand Rapids, MI (Onsite )
Experience : 5 years.
Job description:
Mandatory : Medical device Manufacturing Domain and validation expertise (for North Haven, CT)
Mandatory : Automation validation equipment, validation activities (For Grand Rapids, MI )
Roles & responsibilities:
• Collaborate with Quality Engineering to provide manufacturing support.
• Responsible for providing manufacturing engineering support to specific projects including change analysis, risk analysis, and manufacturing readiness.
• Should be experienced in conducting Time Study for various assembly line.
• Should be experienced in Medical device manufacturing assembly lines.
• Troubleshoot and resolve issues relating to the safety, efficacy, quality, cost, or delivery of components and finished devices.
• Need to conduct qualification, verification, and validation activities to produce medical devices.
• Need to be responsible for completing engineering work and contribute to new product development teams and product support
• Technology development, test of materials or products, preparation of specifications, six sigma, process studies, process improvements, and report preparation.
• Need to design, procure, and fabricate tooling and fixtures.
• Design, document, and improve manufacturing processes and operations that control the safety and efficacy of finished devices.
• Train, develop, and/or provide work direction to operators and technicians.
• Participate on cross-functional project teams. Coordinate, manage, and document project work and progress, and recommend appropriate revisions.
• Participate in design control efforts related to risk analysis (failure mode and effect analysis) & design reviews.
• Work with CFT teams in troubleshooting problems on the production floor.
• Need to identify and implement process/product improvement alternatives to increase/optimise yield, efficiency, throughput, and/or performance.
• Design, develop, testing, and validate equipment and processes; analyse and interpret process models and recommend process improvements.
Qualification:
• BS Degree in Packaging Science, Mechanical Engineering or Equivalent/MS Engineering
• Min 3 yrs. Applicable Experience in packaging engineering, medical devices, pharmaceutical or related industry preferred. Broad knowledge of Mechanical/Manufacturing Engineering.