A Manufacturing Process Engineer develops workflow, work station, and equipment improvement recommendations within a company's manufacturing environment. Fine tunes manufacturing processes by researching, designing, modifying, and testing manufacturing methods and equipment. Evaluates manufacturing processes, applies knowledge of product design, fabrication, assembly, tooling, and material.
View More Jobs Senior Design Quality Engineer (hybrid - Lake Forest, IL) Lake Forest, IL, United States (Hybrid) Be the First to Apply Apply Now 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 to ensure 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 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 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 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. Typically, 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 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. We're ready to bring you consistent quality, innovation, and value in more areas than ever. Our focus allows us to bring you: Dedicated and non-dedicated IV sets and needlefree connectors clinically proven to provide an effective barrier against bacterial transfer and colonization. The industry's broadest IV smart pump offering covering large volume, pain management, and ambulatory needs. IV medication safety software providing full IV-EHR interoperability with the highest customer satisfaction and compatibility with more EHR systems than any other company. Significant US IV solutions manufacturing and supply capabilities.
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.
ICU Medical EEO Policy Statement Know Your Rights:
Part 820, and other applicable regulations and standards. Senior Associate, Regulatory Affairs Lake Forest, IL, United States (Hybrid) Posted on 07/17/2026 Provides regulatory support and expertise associated with global and US registration of medical device products, including in-depth analysis of the requirements and tracking of deliverables. With oversight, supports creation of global regulatory strategies and assists in execution including creation and maintenance of global registration dossiers. Assures full regulatory compliance of all documentation for submissions and change management. See More Jobs
