Date Posted: 12/30/2025
Hiring Organization: Rose International
Position Number: 495021
Industry: Medical Equipment & Supplies
Job Title: Senior Manufacturing Engineer
Job Location: Redmond, WA, USA, 98052
Work Model: Onsite
Shift: M-F, 8 to 5
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 13
Min Hourly Rate($): 65.00
Max Hourly Rate($): 75.00
Must Have Skills/Attributes: Communications, Manufacturing
Experience Desired: Class III Medical Devices (2 yrs); Highly Regulated Industry (2 yrs)
Required Minimum Education: Bachelor’s Degree
Preferred Education: Master’s Degree
**C2C is not available**
Job Description
Required Education:
• Bachelor of Science degree; preferably in Manufacturing, Industrial, or Mechanical Engineering, or equivalent experience
Required Experiences and Skills:
• 5+ years’ experience in process design, development, and process/equipment qualification or validation
• Class III Medical Device, highly regulated environment
• Experience in regulatory industries such as aerospace or medical device manufacturing
• Ability to efficiently collect and analyze data
• Good analytical and organizational skills with the ability to prioritize workload
• Demonstrated communication skills (written and oral)
• Ability to express technically complicated ideas and explain them to others
Senior Manufacturing Engineer Responsibilities:
Works with periodic supervision under the direction of Operations Management and/or with Project Leaders. Will work with Production, Design Engineering, Quality Assurance, Purchasing, and other cross-functional groups in order to improve the manufacturing process. Uses modern engineering methods and various analytical tools to reduce flow time, incorporate upgraded manufacturing technology, improve quality, reduce variability, and reduce the risk of personal injury.
Essential Duties & Responsibilities
• Mission-oriented culture, energized by the knowledge that our products save lives every day, and our work here has a very material impact on the delivery of healthcare around the world.
• Responsible for resolving manufacturing issues from root cause to the most apparent symptoms
• Participate in the development and implementation of reliable methods, working across functional groups
• Develop and implement new manufacturing processes and concepts
• Develop and maintain process documentation
• Develop best practices and implement across all products
• Design, conduct, and develop reports for experiments to characterize and validate new or changed manufacturing processes
• Train assemblers in new manufacturing processes
• Balance the production line
• Justify, specify, order and coordinate the installation and qualification of tooling and equipment
• Evaluate product designs and facilitate DF(X) improvements
• Determine appropriate material presentation and packaging
• Improve ergonomics of manufacturing methods
• Perform other related duties as assigned - **Only those lawfully authorized to work in the designated country associated with the position will be considered.**
- **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**
Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.
California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.
Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.
If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.
Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).
The interactions that I have had with your representatives have always been prompt and very professional. I am very pleased and impressed with your company and services.
Sioe, Consultant
My on-boarding with Rose was outstanding. The packets of information, the process, and great attention to detail each person gave me allowed me to get started quickly.I appreciated each person's friendly and helpful attitude.
Diana, Consultant
As a contractor, I have to say that Rose International was by far the best agency I have worked for.
Q'testdalir, Consultant
Working for Rose International was the most pleasant assignment I have ever had. They were always on top of situations when necessary, and very helpful. I was very proud to be an employee of Rose International, and would recommend anyone to try to work with them.
Melvon, Consultant
Your team at Rose International is always very helpful and responsive.
Barbara, Consultant
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