What are the responsibilities and job description for the Manufacturing Engineer II position at Laborie?
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.
Who We’re Looking For
As a key member of the Operations team, the Manufacturing Engineer II will be responsible for developing and qualifying processes and equipment for the manufacturing of medical devices.
About The Role
Our Mission every day is to operate as a world-class specialist medical company making and advancing technologies that preserve and restore human dignity. We do that today by helping people with pelvic and gastrointestinal conditions live normal lives, and by helping mothers and babies have safe deliveries.
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.
Who We’re Looking For
As a key member of the Operations team, the Manufacturing Engineer II will be responsible for developing and qualifying processes and equipment for the manufacturing of medical devices.
About The Role
- Improve manufacturing efficiency by analyzing and planning workflow, time study, and space requirements, soliciting observations from operators, and equipment layout.
- Write, plan and execute line validation/qualification activities, including IQ, OQ, MSA, and PQ.
- Participate in PFMEA, Process Mapping, and Critical to Quality (CTQ) reviews.
- Create process documentation, including Work Instructions, Control Plans, and Job Safety Analysis sheets.
- Bachelor’s degree in engineering, or equivalent, plus 5 years of experience as a Manufacturing/ Production Engineer, preferably in Medical Devices,
- Experience in process and equipment qualification for medical devices.
- Experience in process improvement.
- Demonstrated knowledge of medical device manufacturing methods (adhesives, machining, molding, extrusion)
- Experience in molding
- Experience in scripting and ladder logic programing
- Electrical, pneumatic, and hydraulic control experience
- Software skills: CAD (SolidWorks), Mini-Tab
Our Mission every day is to operate as a world-class specialist medical company making and advancing technologies that preserve and restore human dignity. We do that today by helping people with pelvic and gastrointestinal conditions live normal lives, and by helping mothers and babies have safe deliveries.
- Paid time off and paid volunteer time
- Medical, Dental, Vision and Flexible Spending Account
- Health Savings Account with Company Funded Contributions
- 401k Retirement Plan with Company Match
- Parental Leave and Adoption Services
- Health and Wellness Programs and Events
