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      Iso jobs in Down at Collins mcnicholas 31 -38 of 38 (0.000s)

      Manufacturing engineer

      GalwayCollins McNicholas

      ...are compliant with GMP, ISO 13485, and regulatory standards.Candidate Requirements Degree in Engineering, Manufacturing, Biomedical, Mechanical, or a related discipline. Minimum 2 years’ experience in a regulated manufacturing environment, ideally medical devices. Strong knowledge of GMP, process validation, and manufacturing [...]

      Category Engineering & Architecture

      30+ days ago in Collins McNicholas

      Senior quality engineer

      GalwayCollins McNicholas

      ...risk in line with ISO 14971. Oversee supplier qualification, audits, and non-conformance management. Approve batch release, product disposition, and key quality decisions.Knowledge, Skills and Experience Required for the Role: Degree in Engineering, Science, or related field. 5+ years’ experience in Medical Device or Pharma [...]

      Category Manufacturing & Production

      30+ days ago in Collins McNicholas

      Qa manager

      GalwayCollins McNicholas

      ...will ensure compliance with ISO 13485, 21 CFR 820, and EU MDR while driving continuous improvement. Ideal for an experienced Quality Manager or Senior Quality Engineer ready to step into leadership.Overview of your responsibilities (full job description available on request) Lead, develop, and support the Quality Engineering [...]

      Category Manufacturing & Production

      30+ days ago in Collins McNicholas

      Manufacturing technician

      GalwayCollins McNicholas

      ...of quality standards, including ISO 13485, MDR, and FDA Requirements. 2-5 years hands-on experience in the Medical device/pharma industry, operating and maintaining production equipment and supporting process improvementsFor a confidential discussion on the Manufacturing Technician role, please contact Emma Barry today.091 [...]

      Category Manufacturing & Production

      30+ days ago in Collins McNicholas

      Senior quality engineer

      GalwayCollins McNicholas

      ...line with FDA and ISO requirements.Knowledge, Skills and Experience Required for the Role: Degree in Engineering, Life Sciences, or related field Level 8 Degree in Science, Engineering, Quality or similar. 5+ years’ experience in the medical device industry. Strong knowledge of quality systems, measurement techniques, FDA & [...]

      Category Engineering & Architecture

      30+ days ago in Collins McNicholas

      Senior quality engineer

      GalwayCollins McNicholas

      ...compliance with FDA QSR, ISO 13485, ISO 14971, MDR and other global regulations. Lead quality support for new product introduction including risk, V&V, process controls, CAPA, and documentation. Develop and maintain process validation (IQ/OQ/PQ), equipment qualification, and test method validation with contract [...]

      Category Engineering & Architecture

      30+ days ago in Collins McNicholas

      Quality systems specialist

      WestmeathCollins McNicholas

      ...21 CFR Part 820, ISO 13485, ISO 27001, and other applicable regulatory requirements. This position supports both internal processes and external audits to uphold product quality and patient safety in the design, manufacture, and distribution of medical devices. This is a permanent opportunity offering hybrid [...]

      Category Banking, Insurance, Finance & Accountancy

      30+ days ago in Collins McNicholas

      Senior clinical research associate

      SligoCollins McNicholas

      ...devices in line with ISO standards, FDA regulations, EU MDR, the company’s Quality Management System, and other applicable requirements.Overview of your responsibilities (full job description available on request): Coordinate clinical investigation activities Work with site staff, consultants, and teams as needed Keep study [...]

      Category Science & Biotech

      30+ days ago in Collins McNicholas
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