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Search Results: 6 vacancies
- ...understanding of outsourced manufacturing, logistics and medical device production processes. ~ Hands-on experience with 21 CFR 820 and ISO 13485 / 9001 standards. ~ Strong track record of building and managing global supplier and partner relationships. ~ Skilled at...SuggestedFull timeContract workFlexible hours
- ...regulatory compliance is upheld at the highest level. You’ll also play a crucial role in upholding and achieving accreditations, including ISO and CARES certifications, and fostering a culture of continuous improvement. What You’ll Do: Health & Safety Leadership: Work...Suggested
Hardwareassociation
Clondalkin, Co. Dublin2 days ago - ...~ Proven expertise in working with outsourced manufacturing, logistics and regulated environments. ~ Familiarity with 21 CFR 820, ISO 13485, and ISO 9001. ~ Strong organizational, communication and leadership skills. ~ Demonstrated ability to manage vendors, budgets...SuggestedFull time
- ...medical device sector. ~ Strong track record managing technically complex projects with cross-functional teams. ~ Familiarity with ISO 13485 and FDA regulatory frameworks. ~ Proficiency in project management tools (MS Project, JIRA, Confluence, SharePoint). ~...SuggestedFull time
- ...communication and leadership skills in a multidisciplinary environment. Experience in clinical governance, laboratory accreditation (ISO 15189), and quality improvement. Expertise in Thoracic, Dermatology-Pathology and cytopathology are required. Why work at the...SuggestedPermanent employmentFull timePart time
- ...Translate complex stakeholder requirements into hardware/software specs and innovative design strategies Ensure functional safety (ISO 26262), cybersecurity (ISO 21434), and production readiness are integrated from the ground up Specify digital requirements for analog...SuggestedFull time
