Senior Design Quality Engineer (hybrid - Lake Forest, IL)

About the role

The Sr. Quality Engineer will be responsible for development procedures and deliverables, ensuring their compliance with ICU Medical quality system requirements and applicable regulations and standards (such as ISO 13485, ISO 14971, 21 CFR Part 820, and other applicable regulations and standards).

Responsibilities

• Effectively utilize quality tools and processes such as product and process controls, risk analysis/management tools, validation, design verification, investigations, CAPA data, etc. to assure product quality.
• Affirms conformance with regulations of the FDA and other international regulatory agencies and may assist in providing responses to the FDA and other regulatory agencies with respect to medical device compliance.
• Provides compliance guidance concerning development, application, and maintenance of quality standards as related to product development within the quality system.
• Work with cross-functional teams to coordinate product changes. Participate in design reviews, test readiness reviews, cross functional teams, risk assessments, design transfers, etc.
• Provide corporate quality support, guidance and direction for bringing on-market product issues to closure and escalating to senior management for support as necessary.
• Ensure that potential product and process risks are evaluated, prioritized, and mitigated to continuously improve product quality.
• Utilize a wide variety of data sources including product review, global complaints, manufacturing quality data, etc. Monitor product data to identify statistically significant trends and risks.
• Ensure compliance, alignment and consistency with ICU Medical’s quality system.
• Prepare, support and ensure the readiness for any potential internal and/or external audits and inspections.
• Work special projects as assigned.

Knowledge & Skills

• Expert quality compliance, audit, and investigation skills
• In depth deep and broad knowledge of Quality Management Systems and experience linking risk management to all elements of the Quality System (Design Controls, CAPA, Complaints, Document Control, etc.)
• Strong knowledge of medical device standards, including but not limited to:ISO 13485ISO 14971ISO 60601
• In depth experience with and knowledge of FDA, MDR, and other key medical device regulations
• Well-developed ability to take a systems approach and to understand the interaction between components (i.e. hardware, software, consumables)
• Proven ability to work closely with engineering and manufacturing team members

Qualifications, Education & Experience

• Must be at least 18 years of age
• Bachelor’s degree in engineering (Electrical, Mechanical, Biomedical, Software) or related field from an accredited college or university is required
• Minimum of seven years of experience in R&D or Quality is required
• ASQ CQE or CSQE certification is desirable

Work Environment

This is largely a sedentary role. This job operates in a professional office environment and routinely uses standard office equipment.

Pay

Salary Range - $105,000 - $150,500

Schedule

The salary range displayed represents the annual base salary we reasonably expect to pay for this role. The actual salary may vary based upon various factors, including, but not limited to, relevant experience, skills, education, licensure/certifications, and geographic location.

Benefits

Competitive financial benefits, including a generous 401(k) match and (for eligible roles) our Annual Incentive Plan
A wide range of benefit options at affordable rates
Additional perks to assist employees with their work-life effectiveness, such as Paid Time Off, Company Holidays, and Tuition Reimbursement
Additional information on health and welfare benefit offerings can be found at https://www.icumed.com/about-us/careers/investing-in-your-future/

About Us

ICU Medical has consistently provided you with clinical innovations that help solve real-world challenges. With the acquisition of Hospira Infusion Systems in 2017 and Smiths Medical in 2022, we are now a global market leader with a complete line of clinically-essential IV therapy and high-value critical care products for hospital, alternate site, and home care settings.

ICU Medical EEO Statement

ICU Medical is committed to being an Equal Opportunity Employer. We ensure that all qualified applicants receive fair consideration for employment regardless of race, color, nationality or national origin, ethnicity, sex, gender, religion or belief, marital or civil partnership status, sexual orientation, pregnancy or maternity, age, disability, or protected veteran status. If you are an individual with a disability and need reasonable accommodation to participate in the employment selection process, please contact us at humanresources@icumed.com. We are committed to providing equal access and opportunities for all candidates.