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Leads medical-device design, prototyping, and regulatory compliance for Medline’s products, using CAD tools and collaborating with cross-functional teams to translate user needs into manufacturable devices.
Validates and audits global suppliers for a medical device manufacturer to ensure compliance with ISO, FDA, and internal quality standards.
Leads the Quality Assurance team at a pharmaceutical manufacturing site, ensuring compliance with regulations like GMP and ISO while driving continuous improvement and product quality.
Job Summary Job Description Oversee and manage the Quality Control functions and personnel at designated distribution center. Responsibilities Include inspection, product disposition, holding and releasing of product…
Job Summary This role must be located in the Chicagoland area. Audit a broad, global supplier base against FDA regulations, ISO standards, and other applicable global regulatory requirements across the full spectrum of…
Job Summary This role needs to be based in commuting distance to our corporate headquarters in Northfield, IL. Relocation assistance may be available for the right candidate. This position requires travel up to 40% of…
Job Summary Job Description JOB SUMMARY: Audit a broad, global supplier base against FDA regulations, ISO standards, and other applicable global regulatory requirements across the full spectrum of Medline products…
Job Summary Job Description Job Summary: Quality engineer is an essential support role for certain division in Medline. He/She will be providing suggestion or comment from quality perspective for other department (i.e…
Job Summary The Senior Design Engineer researches, designs, develops, and supports complex medical devices with a focus on electrical and system design. This role provides technical leadership and subject matter…
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