Sr. Quality Engineer

IMRIS, Deerfield Imaging; Chaska (MN); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Health insurance

401(k) Savings Plan plus matching

Generous paid time off and sick leave

Job summary

IMRIS, Deerfield Imaging, based in Chaska, Minnesota, is seeking a Senior Quality Engineer. This integral role within the Quality Assurance team will ensure compliance and support design verification for medical devices.

The ideal candidate will have a Bachelor's degree in engineering and at least 5 years of relevant experience, with a strong background in FDA regulations and quality standards. Benefits include health insurance, a 401(k) plan, and generous paid leave.

Qualifications

• At least 5 years of experience in engineering or quality.
• Direct experience with FDA inspections and MDSAP audits.
• Ability to read and interpret engineering/technical documents.

Responsibilities

• Analyze medical device products for compliance to standards.
• Author new SOPs and review Change Orders.
• Perform Design History File audits to ensure regulatory compliance.

Skills

Critical thinking

Time management

Oral and written communication

FDA regulations knowledge

Team collaboration

Education

Bachelor of Science (B.S.) degree in engineering

Tools

ISO 13485 standards

ISO 14971 Risk Management

Medical Electrical Equipment Safety Standards

Job description

OVERVIEW

As a global leader in intraoperative MRI, IMRIS Imaging, Inc. delivers fully integrated surgical environments that provide clinicians with real-time MRI and imaging insights during procedures. These solutions are designed to improve clinical decision‑making, enhance surgical precision, and ultimately drive better patient outcomes. The IMRIS Surgical Theatre enables seamless intraoperative imaging directly within the operating room, eliminating the need to move patients and ensuring timely access to critical data when it matters most.

To date, more than 70,000 patients have benefited from procedures performed in IMRIS Surgical Theatres worldwide, supporting improved resection rates, reduced reoperation needs, and extended life expectancy in complex neurosurgical cases.

IMRIS continues to advance the field by integrating next‑generation intraoperative imaging technologies and shaping the future of neurosurgery and image‑guided interventions across leading hospitals globally.

We are searching for a Senior Quality Engineer to join our team. This role will be performed on‑site and is based in the While currently a hybrid position, in‑person engagement is required and the ideal candidate should currently reside in the Greater Twin Cities area.

JOB SUMMARY

The Senior Quality Engineer is a member of the Quality Assurance team that will directly support medical device product after release. This Senior role is responsible for providing support for design verification and validation activities while ensuring compliance to IMRIS design control procedures, Quality Management Systems procedures, and applicable regulations and external standards.

ESSENTIAL DUTIES AND RESPONSIBILITIES

• Analyze medical device products for compliance to standards
• Actively participate in the Design Change process to ensure the proposed changes to the products are systemically and thoroughly analyzed and assessed
• Author new SOPs and other documentation
• Review and approve Change Orders (COs), Nonconformance Report (NCRs) records, Corrective and Preventive Action (CAPA) records, and Deviation Report records. Potential to own quality system NCRs, CAPAs, and project plans relating to Design Assurance and Risk Management
• Work within a cross‑functional team to identify and implement effective controls and support product development from concept through commercialization
• Perform Design History File audits to investigate and monitor compliance with regulatory requirements
• Performs and leads risk management reviews of traceability matrices to ensure correct linking relationships are established between requirements and Verification/Validation records
• Provides compliance guidance concerning development, application, and maintenance of quality standards
• Work directly on Released Product engineering teams
• Perform standards analysis and works with engineering on approach to compliance
• Review verification objective evidence for compliance to standards
• Write design inspection protocols for various products
• Writes quality plans to ensure compliance gaps are addressed
• Assist other functional groups in quality assurance activities and coordinate assigned projects in conjunction with project teams
• Provide guidance to other departments on quality requirementsIdentify sources of quality problems and design corrective action programs
• Assist in the development and/or update of procedures, instructions and methods for inspection, testing, validation/verification, evaluation, recording and reporting quality data
• Prepare, support, and ensure the readiness for any potential internal and/or external audits and inspections
• Implements and maintains ISO 14971 Risk Management requirements within procedures and design documentation

SUPERVISION RECEIVED AND EXERCISED

• Reports to the Vice President of Operations, QARA, and Customer Service
• This position does not supervise any other employees

KNOWLEDGE, SKILLS, AND ABILITIES REQUIREMENTS

• Critical thinker and active listener with good time management skills
• Self‑starter with the ability to quickly learn about new processes with very little information provided
• Oral and written communication skills, including the ability to write technical reports and presentations
• Experience advising senior leadership and applying pre/post market regulations
• Direct experience with FDA inspections, MDSAP audits, ISO 13485 audits, and experience communicating with government authorities
• Experience working with remote teams and comfortable being on computer camera during remote meetings
• Experience working as main Quality Engineering team member on Released Products
• Bachelor of Science (B.S.) degree or higher in engineering and at least 5 years of experience in engineering or Quality
• Knowledge of ISO 14971 Risk Management standard and state‑of‑the‑art requirements
• Knowledge of ISO 62304 Life Cycle Requirements for Medical Device Software
• Knowledge of Medical Electrical Equipment Safety Standards and other Industry Standards (e.g. IEC 60601-1, 60601-2, IEC 60601-2-33, IEC 62368-1, and NEMA MRI related standards)
• Ability to read, analyze and interpret engineering/technical drawings, common scientific, technical and quality/regulatory documents
• Knowledge of regulations, standards and directives for applicable jurisdictions in scope of the IMRIS QMS to include:
  • European MDD 93/42/EEC and EU MDR
  • Canadian Medical Device Regulations (SOR/98-282)
  • MDSAP (Medical Device Single Audit Program)
  • ISO 13485
  • Japanese QMS Ordinance (MHLW MO 169)
  • Australian Therapeutic Goods (Medical Devices) Regulations (TG(MD)R Sch3)
  • US FDA Quality System Regulation, MDR, Recall (21CFR820)
  • CFDA (China) Quality System regulations

Benefits

• Health insurance
• Dental insurance
• 401(k) Savings Plan plus matching
• Flexible Spending Account
• Life Insurance
• Disability Insurance
• Vision Insurance
• Generous paid time off and sick leave
• Incentive Bonus
• Paid Parental Leave

Compensation Disclaimer

The actual rate of pay offered within this range may depend on several factors, such as skills, knowledge, relevant education, experience, and market conditions. Additionally, our organization values pay equity and considers the internal equity of our team when making any offer.

IMRIS is an equal opportunity employer. All qualified applicants will be considered for employment without regard to race, color, religion, sex, age, pregnancy, national origin, physical or mental disability, genetics, sexual orientation, gender identity, veteran status, or any other legally‑protected status.