ICU Medical Inc.

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

ICU Medical Inc.$105K — $150K *
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in engineering (Electrical, Mechanical, Biomedical, Software) or related field required.
  • Minimum of 7+ years in R&D or Quality experience required.
  • ASQ CQE or CSQE certification required or ability to obtain within one year.
  • In-depth knowledge of FDA, MDR, and medical device regulations.
  • Expertise in quality compliance, auditing, and investigation skills.

Responsibilities

  • Utilize quality tools to assure product quality.
  • Ensure regulation compliance with FDA and international agencies.
  • Provide compliance guidance for quality standards in product development.
  • Coordinate product changes with cross-functional teams.
  • Participate in design and test readiness reviews.
  • Offer guidance for resolving on-market product issues.
  • Evaluate and mitigate potential product and process risks.

Benefits

  • Competitive financial benefits including generous 401(k) match and Annual Incentive Plan.
  • A range of affordable benefit options.
  • Paid Time Off and Company Holidays.
  • Tuition Reimbursement to support educational growth.
Full Job Description
Job Description

Position Summary

Provide quality support for ICU Medical Hardware and development. 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). The Sr. Quality Engineer will provide quality assurance support for product realization/manufacturing teams. Reporting to the Quality Manager, this individual will be the Quality Core Team Member for ensuring products are developed/manufactured utilizing appropriate processes to design the highest level of quality into products as they are developed.

Essential Duties & 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.
  • Assures 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 brining 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 13485
    • ISO 14971
    • ISO 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

Minimum 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 7+ years of experience in R&D or Quality is required
  • ASQ CQE or CSQE required or the ability to obtain within one year.

Work Environment
  • This is largely a sedentary role.
  • This job operates in a professional office environment and routinely uses standard office equipment.
  • Typically requires travel 5% to 10% of the time


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

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

ICU Medical provides a comprehensive total rewards package that includes:
  • 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 ICU Medical Inc.

ICU Medical, Inc. is a global medical device company that develops, manufactures, and sells innovative medical products used in vascular therapy, oncology, and critical care applications. The company's products are designed to improve patient outcomes by helping prevent bloodstream infections and protecting healthcare workers and patients from exposure to infectious diseases or hazardous drugs. ICU Medical's product portfolio includes needlefree connectors, closed system transfer devices, and other medical devices and accessories. The company has operations in North America, Europe, and Asia and employs over 5,100 people worldwide.
Learn more about ICU Medical Inc.
Size
8,500 employees
Market Cap
$3.7 billion
Industry
Net Income
$86.8 million
Founded
1984
5 Year Trend
+28.3%
Revenue
$1.2 billion
NASDAQ

Similar Jobs

More Jobs at ICU Medical Inc.

More Healthcare Jobs

Find similar Senior Engineer, Design Quality (Hybrid - Lake Forest, IL) jobs: