Production Associate II, 2nd Shift (Multiple Openings)
Johnson & Johnson is currently seeking a Production Associate I, located in Danvers, MA
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/.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.
We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
Job Summary
The Cleanroom Production Associate II will be responsible for assembling, inspecting and testing high quality medical devices while working within a controlled manufacturing system.
Duties & 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 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
- 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
