What are the responsibilities and job description for the Senior Quality Engineer position at Jacobs Management Group, Inc.?
Step into a role where your work directly supports safer, stronger, more reliable medical products. My client is looking for a Senior Quality Engineer who will play a key role in elevating quality systems, strengthening compliance, and driving meaningful improvements across a growing manufacturing environment. This is your chance to influence products that truly impact lives.
Why You Should Apply
- Opportunity to shape and improve critical quality systems in a regulated environment
- Meaningful impact supporting medical-grade products and customer programs
- High visibility role collaborating across engineering, operations, and leadership
- Competitive benefits and professional development support
What You’ll Be Doing
- Lead improvements for CAPA, complaints, nonconformance, audits, training, and validation
- Develop, implement, and enhance processes to meet quality and business metrics
- Analyze defective product trends and drive corrective actions using statistical tools
- Support customer collaborations, supplier qualifications, and change management
- Maintain documentation aligned with ISO 13485 and FDA QSR
- Lead investigations and develop effective CAPAs
- Conduct internal audits and support regulatory and customer audits
- Serve as Quality Lead when needed
About You
- Be able to do the job as described.
- Hold a bachelor's degree in engineering or science
- Bring experience with ISO 13485, FDA 21 CFR 820, and regulated manufacturing
- Comfortable with statistical process control and process validation
- ASQ certification or Six Sigma training is a plus
Salary : $135,000 - $140,000
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