The Sr. Cleanroom Production Associate will be responsible for assembling, inspecting and testing high quality medical devices while working within a controlled manufacturing system.
Principle Duties and Responsibilities:
Process polymer materials to compose, test, or apply on medical devices
Assemble plastic and metal components into medical devices
Perform in-process quality checks on subassemblies and finished product
Utilize small hand tools, calibrated instruments, measurement equipment, microscopes and test fixtures
Work with engineers and technicians to resolve line issues and suggest improvements
Maintain clean room integrity by using proper attire and adherence to clean room environment practice and procedures
Maintain accurate records/documentation related to quality, work in progress, test results, labor (e.g., timecards), and special projects
Apply workstation practices and line clearance in daily activities
Adhere to general safety rules, manufacturing procedures, company policies and procedures, QSR, and FDA regulations
Skills/Requirements
Job Qualifications:
5 - 8 years of related work experience in medical device assembly with use of microscope required.
High School degree is desired
Must have good hand-eye coordination and manual dexterity to work with small plastic and metal components in a high volume manufacturing setting
Knowledge of lean, kaizen, and continuous improvement initiatives required.
Ability to read, write, and speak English
Ability to utilize basic math skills
Computer literacy required, working knowledge of Microsoft Office Suite required.