Job Description

Available Shifts
1st shift - 7am - 3pm
2nd shift - 3:30pm - 12am

Job 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