Position Summary
This role is critical to ensuring that all processes, equipment, and systems involved in the manufacturing and development of ICU Products meet the highest standards of quality and regulatory compliance. The Quality Engineer II, Sustaining will work closely with cross-functional teams, including R&D, Advanced Manufacturing Engineering, Manufacturing, and Quality Assurance, to validate equipment, processes, and software used in production.
Essential Duties & Responsibilities
- 01Demonstrate an understanding and functional impact of changes to critical process in the manufacturing and testing of ICU products.
- 02Develop and execute validation protocols (IQ/OQ/PQ) for manufacturing equipment, processes, and software systems.
- 03Conduct risk assessments to identify critical quality attributes (CQAs) and critical process parameters (CPPs) for validation.
- 04Create and review Quality Control Plans and process FMEA’s,
- 05Ensure validation documentation is accurate, complete, and in accordance with regulatory and quality system requirements.
- 06Maintain validation master plans, protocols, and reports as part of the company’s quality system documentation.
- 07Improve the Quality Management System through internal audits and supporting regulatory audits.
- 08Lead and support the validation of new and existing manufacturing processes, ensuring compliance with FDA regulations, ISO 13485 standard, and company quality systems.
- 09Develop and execute Test Method Validations for manufacturing processes and laboratory equipment, as needed
- 10Must be able to apply a well-rounded understanding of engineering/design specifications, and engineering principles and methods, to perform analysis and resolve problems of moderate complexity.
- 11Write effective reports and do so in a timely, priority driven manner, working effectively in a team environment with shifting priorities and time sensitive requirements.
- 12Updates Standard Operating Procedures and related QMS documentation, to complete improvement projects, as required.
- 13Establish and maintain communication both internal and external (with the customers, molding, automation, assembly, product engineering, project management and regulatory personnel as needed)
- 14Continually improve knowledge of relevant quality/regulatory topics and changes.
Knowledge, Skills & Qualifications
- 15Knowledge of Agile PLM / Oracle (Desirable)
- 16Knowledge of basic Geometric Dimensioning & Tolerancing (GD&T) concepts.
- 17Proficient in Minitab and Microsoft Office Suite
- 18Strong communication skills and the ability to work collaboratively with cross-functional teams.
- 19Able to multitask and work in a fast-paced environment.
- 20High level of attention to detail and strong organizational skills.
Education and Experience
- 21Must be at least 18 years of age
- 22Bachelor’s degree in STEM from an accredited college or university
- 232-4 years’ experience working in a regulated manufacturing or pharmaceutical/healthcare environment required. Prior experience in quality is preferred.
- 24Proficiency in using validation software and other relevant tools (e.g., Minitab, statistical analysis software).
- 25Strong knowledge of medical device validation processes, risk management, and regulatory requirements (FDA 21 CFR Part 820, ISO 14971, ISO 13485).
Physical Requirements and Work Environment
- 26This is largely a sedentary role.
- 27This job operates in a professional office environment and routinely uses standard office equipment.
- 28Work is partly performed in a clean room environment
- 29Must be able to occasionally move and lift objects of up to 25 lbs
- 30Typically requires travel less than 5% of the time
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
- 31Dedicated and non-dedicated IV sets and needlefree connectors clinically proven to provide an effective barrier against bacterial transfer and colonization.
- 32The industry’s broadest IV smart pump offering covering large volume, pain management, and ambulatory needs.
- 33IV medication safety software providing full IV-EHR interoperability with the highest customer satisfaction and compatibility with more EHR systems than any other company.
- 34Significant 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 icumed.com/media/lwkcbbam/icu-medical-eeo-policy-statement-2025.pdf
Know Your Rights: Workplace Discrimination is Illegal Poster
icumed.com/media/0mrnh211/know_your_right_2023-2.pdf
ICU Medical CCPA Notice to Job Applicants icumed.com/media/1qwexl5a/icu-medical-job-applicant-privacy-notice-october-2024.pdf
Estados Unidos
