Top 5 Biomedical engineer Jobs in Grand Rapids, Mi

Design Engineer
Aspen Surgical —Caledonia, MI
- Full-time
- Bachelor of Science
- Engineering
- Mid-level
5d
Sr Design Engineer
Aspen Surgical —Caledonia, MI
- Full-time
- Bachelor of Science
- Engineering
- Analysis skills
Military Service - U.S. Air Force, Bioenvironmental Engineer
Military Service - U.S. Air Force —Grand Rapids, MI
- From $57,088.25 a year
- Full-time
- Military
- Mid-level
- Health insurance
7d
Planning & Design Coordinator (Hybrid)
Skytron LLC —Grand Rapids, MI
- $21 - $24 an hour
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Profit sharing
- Wellness program
Quick Apply
Director, New Product Development
Aspen Surgical —Caledonia, MI
- Full-time
- Surgery
- Engineering
- Continuous improvement

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Design Engineer

Aspen Surgical -
Caledonia, MI

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Job Details

Full-time
5 days ago

Qualifications

Developing medical devices
Statistics
ASTM standards
Product development project management
ISO standards
Safety regulations
Bachelor's degree in engineering
Quality risk management
Cost analysis
Design controls
Biomedical regulatory compliance
Managing projects
Project risk management
Cross-functional communication
FDA regulations
Failure analysis

Full Job Description

About Aspen
We love what we do! At Aspen Surgical we live our values of Customer Focus, Integrity, Accountability, Collaboration, and Innovative Spirit every day. This caring dedication creates and builds exceptional products that drive the industry standard making a real and lasting impact on people’s lives around the world. We strive to be the best, while providing the tools, resources, and support needed to set our team members up for success.

Summary
The Design Engineer is responsible for Designing medical devices to support the growth, cost profile, and business continuity of Aspen Surgical products while working in a collaborative team environment.

In This Position, You Will Have the Opportunity to:
Medical Device Product Development

Lead projects and evaluate design changes related to existing products to maintain business continuity.
Develop and evaluate medical device designs which meet defined product requirements and are optimized for safe clinical solutions, production, reliability, and overall cost effectiveness for the business.
Execute medical device design history file activities to be compliant with applicable regulations.
Provide technical support to other departments and individuals as necessary in the exploration of new opportunities, complaints etc.
Evaluate proposed changes to existing products and complete deliverables required to implement change through individual efforts or cross-functional teams.
Ensure product changes meet regulations as well as internal and external customer requirements.
Troubleshoot and problem-solve efforts related to product design.
Conduct thorough engineering and data analysis.

Project Management

Manage project schedules, budgets, mitigating risks, and efficient solutioning of issues.
Communicate project plans, track tasks, and manage time to meet project deadlines.
Communicate with leaders status of projects in a clear and efficient manner.

Global Collaboration

Work closely with the portfolio managers to understand clinical and commercial impacts.
Strong communication skills to convey design concepts to clinicians to obtain design direction
Work with manufacturing throughout the development phases to ensure that products are produced in a safe, efficacious, and quality manner while keeping within established time frames
Work with finance to develop product costing to understand impacts of material/design selections
Interface with vendors, manufacturing facilities, and various internal groups to resolve design and manufacturing issues of new and existing products.

What You Need to Succeed in This Position

Bachelor of Science Degree in Engineering is required
A minimum of three to five years of medical device engineering experience
Regulated industry experience that includes, but not limited to, FDA 21CFR820.30, ISO 13485, ISO 14971, MDSAP and European MDD/MDR requirements.
Preferred working knowledge with ISO 11607 regulations and transit testing to ASTM 4169 or similar testing standards
Strong familiarity with the methods of Risk Management and Failure Mode Effects Analysis (FMEA)
Working knowledge of design history & technical file within an auditing environment.
Working knowledge of statistical analysis of data used to meet or define design criteria
Project management experience to effectively manage and complete multiple projects simultaneously
Preferred involvement with invention disclosures or patents
Business case development for product costing as it pertains to design
Preferred experience using engineering programs such as SolidWorks, Minitab, TOPS, similar.
Strong teamwork and effective communication to enhance a positive culture.
Ability to effectively communicate and collaborate globally.
Drives a culture of clinical safety and quality first.
Mitigates risks during the lifetime of the projects
Engage in continuous education to maintain job knowledge in medical device design & development
Excellent computer skills including but not limited to Microsoft Office Suite
Ability to travel up to 15% required.

We're proud to be an equal opportunity employer- and celebrate our employees' differences, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or Veteran status. Diversity makes us better.

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biomedical engineer jobs in grand rapids, mi

Design Engineer

Sr Design Engineer

Military Service - U.S. Air Force, Bioenvironmental Engineer

Planning & Design Coordinator (Hybrid)

Director, New Product Development

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