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Form of workJob Description
The Cleanroom Production Associate II 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 per approved manufacturing procedures
• Assemble plastic and metal components into medical devices in accordance with approved manufacturing procedures
• Perform in-process quality checks on subassemblies and finished product
• Utilize small hand tools, calibrated instruments, measurement equipment, microscopes, and test fixtures
• Participate in line meetings as needed
• Work with engineers and technician to resolve line issues and suggest improvements
• Maintain clean room integrity by using proper attire and adherence to clean room environment practice and procedures
• Fully understand and maintains 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
Job Qualifications (minimum requirements):
• High School Graduate or equivalent manufacturing experience
• 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, six sigma, kaizen, and continuous improvement initiatives a plus.
• Ability to read, write, and speak English
• Ability to utilize basic math skills
• Execute tasks in a timely manner under general supervision.
• Computer literacy required, Working knowledge of Microsoft Office Suite desired
• Meet all requirements outlined for Production Associate I INSERT PA1 Requirements.
• 4 or more years of medical device manufacturing experience with relevant microscope experience or 2 or more years of intensive microscope job related experience in a Class III medical device company
Principle Duties and Responsibilities:
• Process polymer materials to compose, test, or apply on medical devices per approved manufacturing procedures
• Assemble plastic and metal components into medical devices in accordance with approved manufacturing procedures
• Perform in-process quality checks on subassemblies and finished product
• Utilize small hand tools, calibrated instruments, measurement equipment, microscopes, and test fixtures
• Participate in line meetings as needed
• Work with engineers and technician to resolve line issues and suggest improvements
• Maintain clean room integrity by using proper attire and adherence to clean room environment practice and procedures
• Fully understand and maintains 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
Job Qualifications (minimum requirements):
• High School Graduate or equivalent manufacturing experience
• 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, six sigma, kaizen, and continuous improvement initiatives a plus.
• Ability to read, write, and speak English
• Ability to utilize basic math skills
• Execute tasks in a timely manner under general supervision.
• Computer literacy required, Working knowledge of Microsoft Office Suite desired
• Meet all requirements outlined for Production Associate I INSERT PA1 Requirements.
• 4 or more years of medical device manufacturing experience with relevant microscope experience or 2 or more years of intensive microscope job related experience in a Class III medical device company
2nd Shift - 3:30pm - 12am
10% differential to base pay for 2nd Shift
