Senior Design Assurance Engineer
Maple Grove MN Direct-Hire $105000$135000 Onsite
Konik is working with a medical device client who is seeking a Senior Design Assurance Engineer to provide technical leadership and ensure that new and existing medical device designs meet the highest standards of quality safety and regulatory compliance. This role is central to the product development lifecycle partnering closely with engineering quality and regulatory teams to develop verify and validate design solutions that improve patient outcomes. The ideal candidate combines strong technical expertise with a collaborative mindset and a passion for driving continuous improvement in design assurance practices.
Key Responsibilities
- Lead design assurance activities across multiple product development programs ensuring compliance with internal and external quality standards.
- Collaborate with cross-functional teams to define and implement design control strategies throughout concept design verification and validation phases.
- Develop and maintain risk management documentation including FMEAs hazard analyses and control plans.
- Generate and execute test methods protocols and reports to verify design performance and regulatory compliance.
- Prepare and review Design History Files (DHF) Device Master Records (DMR) and related technical documentation to support audits and submissions.
- Interpret and apply applicable quality and regulatory standards (FDA ISO IEC) during all phases of development.
- Provide technical input during design reviews and offer data-driven recommendations to strengthen product reliability and safety.
- Analyze verification and validation data ensuring test outcomes support design intent and meet acceptance criteria.
- Stay current on evolving global regulations standards and industry best practices related to design assurance and risk management.
- Support and mentor team members by sharing expertise in quality systems and regulatory expectations.
Minimum Qualifications
- Bachelors degree in Mechanical Engineering Biomedical Engineering or a related technical discipline (Masters preferred).
- Minimum of 5 years of experience in design assurance quality engineering or design controls within the medical device industry.
- Strong working knowledge of design control risk management and quality system requirements.
- Experience authoring and reviewing technical documentation for regulatory submissions.
- Proficiency with statistical analysis software and application of statistical methods to validation and verification processes.
- Familiarity with FDA QSR ISO 13485 ISO 14971 and IEC 60601 standards.
- Excellent written and verbal communication skills with a collaborative cross-functional approach.
- Proven problem-solving skills with strong attention to detail and analytical reasoning.
Preferred Skills
- Experience supporting Class II or III medical devices through the full product lifecycle.
- Strong background in verification and validation strategy development.
- Understanding of usability engineering biocompatibility and sterilization validation.
- Hands-on experience leading design reviews and addressing CAPA or audit findings.
- Knowledge of DHF/DMR structure and documentation best practices.
Benefits & Compensation
- Competitive base salary commensurate with experience.
- Comprehensive medical dental and vision insurance.
- 401(k) plan with company match.
- Paid time off including vacation holidays and personal days.
- Short- and long-term disability life insurance and optional voluntary benefits.
- Professional development opportunities in a collaborative growth-oriented work environment.
Be the first to learn about future positions by joining our Newsletter and following us on LinkedIn!
Konik is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race religion color national origin sex sexual orientation gender identity age status as a protected veteran status as a qualified individual with a disability or any other protected class status.
Konik has been creating impactful relationships between technical talent and employers for more than 50 years. Konik has specialized in placing professional qualified personnel in Minnesota and western Wisconsin businesses since its inception and maintains a strong commitment to customer service.
Required Experience:
Senior IC
Senior Design Assurance EngineerMaple Grove MN Direct-Hire $105000$135000 OnsiteKonik is working with a medical device client who is seeking a Senior Design Assurance Engineer to provide technical leadership and ensure that new and existing medical device designs meet the highest standards of qua...
Senior Design Assurance Engineer
Maple Grove MN Direct-Hire $105000$135000 Onsite
Konik is working with a medical device client who is seeking a Senior Design Assurance Engineer to provide technical leadership and ensure that new and existing medical device designs meet the highest standards of quality safety and regulatory compliance. This role is central to the product development lifecycle partnering closely with engineering quality and regulatory teams to develop verify and validate design solutions that improve patient outcomes. The ideal candidate combines strong technical expertise with a collaborative mindset and a passion for driving continuous improvement in design assurance practices.
Key Responsibilities
- Lead design assurance activities across multiple product development programs ensuring compliance with internal and external quality standards.
- Collaborate with cross-functional teams to define and implement design control strategies throughout concept design verification and validation phases.
- Develop and maintain risk management documentation including FMEAs hazard analyses and control plans.
- Generate and execute test methods protocols and reports to verify design performance and regulatory compliance.
- Prepare and review Design History Files (DHF) Device Master Records (DMR) and related technical documentation to support audits and submissions.
- Interpret and apply applicable quality and regulatory standards (FDA ISO IEC) during all phases of development.
- Provide technical input during design reviews and offer data-driven recommendations to strengthen product reliability and safety.
- Analyze verification and validation data ensuring test outcomes support design intent and meet acceptance criteria.
- Stay current on evolving global regulations standards and industry best practices related to design assurance and risk management.
- Support and mentor team members by sharing expertise in quality systems and regulatory expectations.
Minimum Qualifications
- Bachelors degree in Mechanical Engineering Biomedical Engineering or a related technical discipline (Masters preferred).
- Minimum of 5 years of experience in design assurance quality engineering or design controls within the medical device industry.
- Strong working knowledge of design control risk management and quality system requirements.
- Experience authoring and reviewing technical documentation for regulatory submissions.
- Proficiency with statistical analysis software and application of statistical methods to validation and verification processes.
- Familiarity with FDA QSR ISO 13485 ISO 14971 and IEC 60601 standards.
- Excellent written and verbal communication skills with a collaborative cross-functional approach.
- Proven problem-solving skills with strong attention to detail and analytical reasoning.
Preferred Skills
- Experience supporting Class II or III medical devices through the full product lifecycle.
- Strong background in verification and validation strategy development.
- Understanding of usability engineering biocompatibility and sterilization validation.
- Hands-on experience leading design reviews and addressing CAPA or audit findings.
- Knowledge of DHF/DMR structure and documentation best practices.
Benefits & Compensation
- Competitive base salary commensurate with experience.
- Comprehensive medical dental and vision insurance.
- 401(k) plan with company match.
- Paid time off including vacation holidays and personal days.
- Short- and long-term disability life insurance and optional voluntary benefits.
- Professional development opportunities in a collaborative growth-oriented work environment.
Be the first to learn about future positions by joining our Newsletter and following us on LinkedIn!
Konik is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race religion color national origin sex sexual orientation gender identity age status as a protected veteran status as a qualified individual with a disability or any other protected class status.
Konik has been creating impactful relationships between technical talent and employers for more than 50 years. Konik has specialized in placing professional qualified personnel in Minnesota and western Wisconsin businesses since its inception and maintains a strong commitment to customer service.
Required Experience:
Senior IC
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