Production Associate I

Abiomed, part of Johnson & Johnson MedTech is recruiting for a Production Associate I located in Danvers, MA.

There is an internal pre-identified candidate for consideration. However, all applications will still be reviewed.

About Johnson & Johnson

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.

I Am Abiomed | I Am Heart Recovery | Patients First!

Job Responsibilities:

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