Assembler II

Laborie Medical Technologies Corp•Plymouth, MN

39d

About The Position

As a key member of the Operations team, the Assembler II will assemble, inspect, and package and kit the Company’s medical device products. Work location is currently Plymouth, but candidates should be open to a potential move to another site within 15 miles, depending on future operational requirements. About the Role: Prepare and assembler materials, manufacture medical devices in a controlled environment and test products and subassemblies for functionality or quality. Complete lot history records (LHR) during manufacturing and inspect products for quality and adherence to specifications. Handling raw and finished goods materials, facilitating their movement within the plant to support production processes. Ensure materials are accurately received, inspected, stores and delivered to appropriate areas, ensuring compliance with quality standards and production schedules. Assist with process and product qualification activities; conduct regular inventory checks. Show constant attention to detail and immediately inform supervisor of anything out of the ordinary or anything which does not conform to the approved process sheets. Conduct quality self-inspection of all assemblies processed. Complete training and understand documentation needed to comply with Laborie's quality system policies and procedures. Adhere to company policies in terms of punctuality and availability and conform to other policies as described in Company's employee handbook.

Requirements

High school diploma or GED; technical or vocational certificates preferred but not required.
Experience with medical device manufacturing in a cleanroom.
Must be able to read and understand work instructions and safety guidelines and communicate in English.
Individuals will need to stand or sit for extended periods, and work at a cleanroom table height ranging from 30"-40" in a sitting or standing position depending on the workstation.
Basic computer skills including MS Office.

Nice To Haves

Knowledge of good documentation practices, GMP, CGMP a plus.

Responsibilities

Prepare and assembler materials
Manufacture medical devices in a controlled environment
Test products and subassemblies for functionality or quality
Complete lot history records (LHR) during manufacturing
Inspect products for quality and adherence to specifications
Handling raw and finished goods materials, facilitating their movement within the plant to support production processes
Ensure materials are accurately received, inspected, stores and delivered to appropriate areas, ensuring compliance with quality standards and production schedules
Assist with process and product qualification activities
Conduct regular inventory checks
Show constant attention to detail and immediately inform supervisor of anything out of the ordinary or anything which does not conform to the approved process sheets
Conduct quality self-inspection of all assemblies processed
Complete training and understand documentation needed to comply with Laborie's quality system policies and procedures
Adhere to company policies in terms of punctuality and availability and conform to other policies as described in Company's employee handbook.