Assembler II

We believe that great healthcare is an essential safeguard of human dignity. At Laborie, we know the work we do matters – it’s what fuels our motivation and contributes to our success. If you’re ready to make a positive impact in the lives of patients across the globe, we’d like to meet you. We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good. We’re not afraid to roll up our sleeves to make our goals a reality and work together to solve for our customers. We reward and recognize our employees based on our values of Aspire to Greatness, Respect All, Own It, Working Together, Persist with Passion.

About the Role

• Prepare and assemble 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.
• Handle raw and finished goods materials, facilitating their movement within the plant to support production processes.
• Ensure materials are accurately received, inspected, stored, 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.

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.

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

Benefits

• Paid time off and paid volunteer time
• Medical, Dental, Vision and Flexible Spending Account
• 401k Retirement Plan with Company Match
• Parental Leave and Adoption Services
• Health and Wellness Programs and Events
• Awarded 2025 Cigna Healthy Workforce Designation Gold Level