Responsibilities and Requirements: Performs any combination of tasks involved in the fabrication, manufacture, assembly, testing and packaging of medical devices as well as setting up, operating, performing maintenance on and troubleshoot...
Note: Steel toed shoes Interviews in person Requirements: o High school diploma or equivalent., o 1-2 year of manufacturing assembly experience with packaging exp o Must be able to work flexible and/or extended hours and report to wor...
Responsibilities : Work with cross-functional teams to provide regulatory guidance during the development of Class III Medical Devices Establish the regulatory strategy and global registration plan for products, meeting internal quality ...
Responsibilities: 6 years relevant experience in medical device manufacturing. Clean room environment experience. Experience with Test Method Validation and/or Measurement System Analysis is preferred. Knowledge of computer software fo...
Responsibilities: Bachelor of Science in Engineering, B.E. / B.Tech. Mechanical Engg. / M.S. Mech. Engg. 3 years relevant experience in Medical Device Manufacturing. Clean room environment experience. Experience with Test Method Valida...
Responsibilities and Requirements: This role is responsible for ensuring daily safety, quality, output, and productivity goals for specified departments of responsibility, are met. The Manufacturing Lead will spend 50% of their time in d...
Responsibilities and Requirements: Process and equipment qualification (IQ/OQ/PQ). Development of test methods for Design V&V, Process Validation, and Production. Validation of test methods. Execution of Engineering Builds, Gauge R&R S...
Responsibilities: The experience I am looking for is as follows. 6 years relevant experience in medical device manufacturing. Clean room environment experience. Experience with Test Method Validation and/or Measurement System Analysis ...
Responsibilities: Serve as the senior and principal regulatory affairs member of project development teams, primarily focused on (but not limited to) drug products. Provide regulatory oversight and guidance to project teams on compliance...
Responsibilities: Regulatory submissions including Original ANDAs, Amendments, Annual Reports, Supplements and PADERs to company applications. Preparation/Review of Original submission/Amendments/ Supplements as assigned by the Director,...
Responsibilities: Under the supervision of the Manufacturing Facilitator or designee, the Material Coordinator / material handler is responsible to coordinate and expedite the flow of work and materials within or between production lines ...
Responsibilities Pallet/Case Picking Processing customer orders including but not limited to: scanning bar codes, picking and labeling boxes. Pick, pack and process orders. Processing orders through RF technology. Maintains an accepta...
Responsibilities: Performs instrument optimization functions after final assembly: laser alignment, pressure adjustments, electrical adjustments, etc. Performs final production testing and inspection to ensure products meet performance s...
Responsibilities: Processing customer orders including but not limited to: scanning bar codes, picking and labeling boxes. Pick, pack and process orders. Processing orders through RF technology. Maintains an acceptable work area as out...
Responsibilities: Performs instrument optimization functions after final assembly: laser alignment, pressure adjustments, electrical adjustments, etc. Performs final production testing and inspection to ensure products meet performance s...
Responsibilities: Performs any combination of tasks involved in the fabrication, manufacture, assembly, testing and packaging of medical devices as well as setting up, operating, performing maintenance on and troubleshooting equipment. M...
Responsibilities: Performs instrument optimizati on functions after final assembly: laser alignment, pressure adjustments, electrical adjustments, etc. Performs final production testing and inspection to ensure products meet performance ...
Responsibilities: Conducting and overseeing test method validation, ensuring adherence to quality standards. Designing and implementing protocols for validation processes. Managing and navigating documentation effectively. Qualifying t...