Manufacturing Engineer Manager oversees the development and implementation of manufacturing processes to maintain proper product functionality as well as cost efficiency. Ensures the engineering team and other manufacturing departments work together cohesively. Being a Manufacturing Engineer Manager is responsible for the development of equipment to aid in the manufacturing process. Reviews, evaluates and implements engineering changes and specification requirements. Additionally, Manufacturing Engineer Manager requires a bachelor's degree. Typically reports to a director. The Manufacturing Engineer Manager manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. To be a Manufacturing Engineer Manager typically requires 5 years experience in the related area as an individual contributor. 1-3 years supervisory experience may be required. Extensive knowledge of the function and department processes. (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.