Exp Op Manu Assmb
About The Position
The 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 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 fixture Participate in line meetings as needed 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
Requirements
- High School graduate or equivalent manufacturing experience required
- Must have good hand-eye coordination and manual dexterity to work with small plastic and metal components in a high volume manufacturing setting
- 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
Nice To Haves
- 2 years of related work experience desired.
- Medical device experience preferred.
- Knowledge of lean, six sigma, kaizen, and continuous improvement initiatives a plus.
- Working knowledge of Microsoft Office Suite desired
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 fixture
- Participate in line meetings as needed
- 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
Benefits
- Vacation –120 hours per calendar year
- Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
- Holiday pay, including Floating Holidays –13 days per calendar year
- Work, Personal and Family Time - up to 40 hours per calendar year
- Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
- Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
- Caregiver Leave – 80 hours in a 52-week rolling period10 days
- Volunteer Leave – 32 hours per calendar year
- Military Spouse Time-Off – 80 hours per calendar year
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
