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Senior Quality Engineer, Design
hace 1 mes
Direct message the job poster from ICU MedicalHuman Resources Professional, SHRM-CP, HRBPPosition SummaryProvide quality support for ICU Medical Product and Development and design changes. 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.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.Knowledge & SkillsExpert quality compliance, audit, and investigation skillsIn 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 14971In depth experience with and knowledge of FDA, MDR, and other key medical device regulationsWell-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 membersMinimum Qualifications, Education & ExperienceMust be at least 18 years of ageBachelor’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 requiredASQ CQE or CSQE required or the ability to obtain within one year.Seniority levelSeniority levelMid-Senior levelEmployment typeEmployment typeFull-timeJob functionJob functionEngineering and Information TechnologyIndustriesMedical Equipment ManufacturingReferrals increase your chances of interviewing at ICU Medical by 2xSign in to set job alerts for “Quality Engineer” roles.Tijuana, Baja California, Mexico 8 hours agoTijuana, Baja California, Mexico 1 month agoTijuana, Baja California, Mexico 1 month agoTijuana, Baja California, Mexico 1 month agoTijuana, Baja California, Mexico 22 hours agoSoftware Engineer (Python/Linux/Packaging)We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr
