Quality Engineer

JOB TITLE: Quality Engineer

JOB LOCATION: Ramsey, MN

JOB TYPE: Full Time/40hrs per week

DEPARTMENT: Quality Management

REPORTS TO: Quality Manager

DIRECT REPORTS: No Direct Reports

SALARY: $75,000 - $100,000 (based on experience)

Dynamic Group is a leader in precision manufacturing and custom injection molding for the medical device and related industries. With a commitment to excellence, innovation, and customer satisfaction, we pride ourselves on delivering quality products while fostering a collaborative and inclusive work environment. Our team is driven by our core values: compassion, integrity, determination, respect, and gratitude, and we strive to empower our employees to achieve personal and professional growth.

The Quality Engineer (QE) provides quality engineering support to medical molding manufacturing and product realization processes to ensure quality, compliance, and productivity expectations are met. This role supports both New Product Introduction (NPI) and existing production through validation, data analysis, metrology, and cross‑functional collaboration with Engineering, Operations, and Quality.

The QE role is a technical and analytical position that blends hands‑on engineering support with parts, validation focus, documentation, reporting, and continuous improvement activities.

*** This is a Full‑time, in‑office role in Minnesota. Candidates must reside in MN and relocation assistance are NOT offered***

• Serve as a quality interface for Engineering and Production related to customer requirements, validations, and quality concerns.
• Provide quality engineering support for both new and existing products, tools, and processes.
• Collaborate with Engineering on process development, refinement, and ongoing validation activities.
• Support manufacturing with problem‑solving, root cause analysis, and corrective and preventive actions (CAPA).

• Lead and support validation activities for processes, equipment, and metrology systems (IQ, OQ, PQ).
• Develop validation protocols, plans, and reports.
• Analyze and interpret validation and process data to ensure compliance and capability.
• Oversee and support software validation activities as required.
• Ensure adherence to ISO 13485 and applicable FDA regulatory requirements.

• Perform statistical analysis, trending, and reporting of quality and process data.
• Support and develop measurement strategies, inspection plans, and best measurement practices.
• Utilize inspection and metrology equipment including CMM, VMM, and other quality tools.
• Support CMM programming and advanced metrology analysis (Zeiss experience preferred).

• Use data‑driven methods to identify waste, variation, and opportunities for improvement.
• Participate in internal process improvement initiatives.
• Support cross‑functional teams including Engineering, Operations, and Quality to ensure robust and repeatable processes.
• Assist with print and inspection interpretation and ensure customer requirements are clearly understood and met.

• Maintain strong documentation practices and compliance with internal and external standards.
• Travel as required to support customer and supplier needs.
• Continuously seek opportunities to improve quality systems, processes, and the customer experience.

• Bachelor’s Degree in Quality, Mechanical, Industrial, or another Engineering discipline.
• Minimum of 3 years of experience in an engineering or quality role within a manufacturing or machining environment.
• Working knowledge of inspection equipment including CMM, VMM, calipers, micrometers, gauges, drop indicators, and other quality tools.
• Experience applying statistics and data analysis methods such as control charts, sampling plans, Gage R&R, and DOE.

• Strong problem‑solving and analytical skills.
• Solid understanding of process capability and validation principles.
• Proficient understanding of GD&T.
• Effective written and verbal communication skills.
• Strong documentation and technical writing…