Manufacturing Engineer Manager jobs in Connecticut

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.