Quality Engineer at Jobot
Kentwood, MI 49512
About the Job
Quality Engineer needed for nationwide leader in precision-machined highly engineered medical products!
This Jobot Job is hosted by: Colin Callahan
Are you a fit? Easy Apply now by clicking the "Quick Apply" button
and sending us your resume.
Salary: $75,000 - $100,000 per year
A bit about us:
We specialize in precision-machining for highly engineered implants and surgical instruments, leveraging decades of expertise in CNC milling, turning, and cutter grinding. With a focus on enhancing medical device functionality, our engineering team collaborates closely with customers, providing Design for Manufacturability consultations that add significant value to the entire process. Our culture prioritizes our employees, offering a generous health care plan, air-conditioned workspaces, and opportunities for debt-free education, fostering a supportive environment built on trust, fairness, and respect.
Why join us?
1. Strong compensation and benefits
2. Amazing team, work environment, and company culture
3. Great vertical mobility and career growth potential!
Job Details
Requirements
Nice to Haves:
Skills/Competencies
Job Responsibilities
Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.
This Jobot Job is hosted by: Colin Callahan
Are you a fit? Easy Apply now by clicking the "Quick Apply" button
and sending us your resume.
Salary: $75,000 - $100,000 per year
A bit about us:
We specialize in precision-machining for highly engineered implants and surgical instruments, leveraging decades of expertise in CNC milling, turning, and cutter grinding. With a focus on enhancing medical device functionality, our engineering team collaborates closely with customers, providing Design for Manufacturability consultations that add significant value to the entire process. Our culture prioritizes our employees, offering a generous health care plan, air-conditioned workspaces, and opportunities for debt-free education, fostering a supportive environment built on trust, fairness, and respect.
Why join us?
1. Strong compensation and benefits
2. Amazing team, work environment, and company culture
3. Great vertical mobility and career growth potential!
Job Details
Requirements
- 5+ years of relevant experience in manufacturing capacity.
- Working Knowledge of ISO 9000 based requirements and related systems
- Proven problem solving experience.
- Ability to work in an entrepreneurial, fast-pace and rapidly evolving environment.
Nice to Haves:
- Green Belt or ASQ certification a plus.
- Bachelor’s Degree in an Engineering or Science discipline. Willing to consider alternate Bachelor Degree programs with relevant experience
- An understanding of GMP for Medical Devices FDA 21 CFR Part 820 Quality System Regulation and ISO 13485 Medical Devices – Quality Management Systems or experience working in a regulated industry.
Skills/Competencies
- Strong interpersonal and presentation skills needed to interact with external customers as well as with all levels within the company.
- Must demonstrate excellent writing skills with ability to prepare/review and/or approve technical documentation.
- Thorough knowledge and experience surrounding machining and quality inspection.
- Proficiency in Microsoft Office Software, and Solidworks.
- Project Management and Lean Manufacturing experience.
- Good knowledge of statistical tools, ability to manage multiple tasks.
- Must be flexible and adapt to changing environments and priorities.
- Proven ability to collaborate in a team environment.
- Demonstrated entrepreneurial skills with the ability to work effectively in a fast paced and changing environment with multiple priorities.
- Excellent communication and interpersonal skills.
Job Responsibilities
- Oversee APQP and PPAP processes: Manage manufacturing changes or new product launches, guiding projects from purchase order to PPAP completion.
- Design for Manufacturability: Provide feedback to customers and implement design improvements for manufacturing efficiency.
- Research and Development: Conduct testing and validation to ensure process effectiveness and compliance with quality standards.
- Technical Documentation: Develop and revise documentation for manufacturing processes, equipment qualification, setup, and maintenance procedures.
- Metrology and GD&T: Develop inspection and test methods for products and processes, utilizing control and sampling plans.
- Equipment Improvement: Evaluate machinery, recommend improvements, and manage new equipment procurement and setup.
- Statistical Analysis: Apply statistical methods for capability analysis, control charting, hypothesis testing, and Gage R&R.
- Continuous Improvement: Lead quality improvement projects, using lean manufacturing tools to optimize processes and reduce waste.
- Corrective Actions: Drive corrective and preventive actions for product quality issues and verify effectiveness.
- Compliance and Reporting: Ensure compliance with ISO and FDA requirements, prepare reports, and recommend process updates based on data analysis.
- Supplier Development: Establish and participate in supplier qualification and development activities.
- Technical Support and Training: Provide troubleshooting and training to production employees and support cross-functional teams.
Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.
Salary
75,000 - 100,000 /year