Job Details

ID #51122321
Estado California
Ciudad San diego
Full-time
Salario USD TBD TBD
Fuente Actalent
Showed 2024-02-24
Fecha 2024-02-25
Fecha tope 2024-04-25
Categoría Etcétera
Crear un currículum vítae

Manufacturing Engineer

California, San diego, 92101 San diego USA

Vacancy caducado!

Description: Be actively involved in selecting, sourcing, testing and approving materials to achieve specifications and reliability requirements. Design, develop, modify and qualify processes and methods for the manufacture, molding and utilization of metallic, plastic, composite and other materials in construction and production of hardware, electronic components and structures. Set-up and qualify manufacturing and test equipment for production line duplication. Determine equipment parameters and analyze the outputs for all the manufacturing, test and packaging equipment. Develop and execute test methods including fixturing and validate test methods for product evaluation. Create ECOs’ (Engineering Change Orders), DCOs' (Document Change Requests) Plans, Protocols and Reports under broad direction. Create and / or update production work instructions. Support qualification of manufacturing equipment changes / process / testing and inspection, and ensure compliance to quality standards through the creation and execution of protocols. Create and maintain the technical documentation for building a complete device master record.Skills:design for manufacturing, engineering change orders, catheter, iso 13485, fdaTop Skills Details:design for manufacturing,engineering change orders,catheterAdditional Skills & Qualifications: Bachelor of Engineering with working knowledge of engineering principles and at least 5 years’ related experience and/or training in sustaining/manufacturing engineering in the medical device industry. Demonstrated medical device design experience required specifically with sterile medical devices; catheter manufacturing engineering experience preferred. Effective Communication skills. Demonstrate good approach to problem solving and project management. Knowledge and Interpretation of FDA guidelines and ISO 13485 requirements. Demonstrated utilization of Design for Manufacture/Assembly and Design for Test methodologies highly desirable.Experience Level:Expert LevelAbout Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

Hiring diverse talent

Maintaining an inclusive environment through persistent self-reflection

Building a culture of care, engagement, and recognition with clear outcomes

Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] (%[email protected]) for other accommodation options.

Vacancy caducado!

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