Job Details

ID #44643204
State California
City Pointmugunawc
Job type Permanent
Salary USD TBD TBD
Source The Davis Companies
Showed 2022-08-06
Date 2022-08-04
Deadline 2022-10-03
Category Et cetera
Create resume

Senior Mechanical Engineer (Sustaining)

California, Pointmugunawc, 93042 Pointmugunawc USA

Vacancy expired!

Are you looking to join a high performing collaborative team in the medical device field? Are you experienced in transitioning medical/surgical devices from R&D to manufacturing (NPI)? Explore this unique opportunity to impact both product development and manufacturing, leveraging mechanical design skills and understanding of manufacturing processes by applying to this posting today!

Position Description: Sr. Mechanical Engineer (Medical Device Sustaining)

As a member Product Development, the position will be responsible for supporting existing products as well as the development of new medical devices in a regulated design control process. This person is expected to have a strong background in manufacturing processes. The product development team includes a diverse set of responsibilities that must be directed by this individual, including new product development, sustaining engineering, and field support interfacing with sales associates and surgeons.

Key Responsibilities:

1. Participate in the entire product development process for medical devices in a regulated design controls environment.

2. Work closely with manufacturing engineers to address prototyping, mechanical assembly, testing, manufacturing control, troubleshooting and inspection processes.

3. Support exiting commercial products with manufacturing, driving improvements, supplies and field issues.

4. Designing parts, fixtures and test setups using 3D CAD tools.

5. Demonstrated understanding of manufacturing processes including injection molding, machining, laser welding and process engineering capability.

6. Responsible for writing required documents including requirements, design, test, engineering reports, verification and validation plan and report.

7. Responsible for communicating with vendors and customers regarding product and project-based needs as well as for maintenance and troubleshooting.

8. Interact with Technicians, Product development, Regulatory Affairs, Sales & Marketing, Quality Assurance, Supply Chain Management, and external suppliers.

9. Lead DFM discussion and provide effective feedback on design activities to improve efficacy, manufacturability, and cost.

10. Travel may be required occasionally.

Education and Experience (Knowledge, Skills & Abilities)

• Bachelor of Science in Mechanical Engineering. Master's degree preferred.

• Minimum 5 years of experience in medical device development under a regulated design control process.

• Experience in mechanical design of electro-mechanical medical devices. Experience transferring designs to manufacturing a plus.

• Strong analytical skills with the ability to define problems, collect data, establish facts, and draw valid conclusions.

• Good communication (oral and written), presentation, and interpersonal skills.

• Strong 3D CAD skillset for designing parts, fixtures and test setups.

• Takes ownership of new products during pilot production phase through successful and sustained project launch

• This includes driving new product introduction schedules, Experience in managing vendors.

DAVIS Companies partners with the top employers locally and nationally. They choose us because of our reputation for finding high quality talent, fast, but also our experience for evaluating and representing the best candidates in the marketplace. We make every effort to provide updates and feedback to candidates at each stage of the process as we appreciate how stressful looking for a new role can be. Apply today and experience "The DAVIS Difference".

#piqaccPandoLogic.Category: Engineering, Keywords: Manufacturing Engineer

Vacancy expired!

Subscribe Report job