- Beckman Coulter Life Sciences (Indianapolis, IN)
- …projects for Beckman Coulter Life Science.Coaching teams with application of ISO 9001/13485/cGMP/IEC 62304 and quality systems processes throughout product ... or MS+4 years' experience in product development, manufacturing and / or quality systems ( ISO 9001), medical device ( ISO 13485), pharmaceutical, related life… more
- Cytiva (Miami, FL)
- …communications. Experience with supplier communication and supplier auditing.Demonstrated knowledge of Quality Management System ( ISO 9001 or equivalent), cGMP, ... about the Danaher Business System which makes everything possible.The Senior Supplier Quality Engineer (m/f/d) for Cytiva is responsible to manage supplier defects,… more
- Cytiva (Miami, FL)
- …communications. Experience with supplier communication and supplier auditing.Demonstrated knowledge of Quality Management System ( ISO 9001 or equivalent), cGMP, ... about the Danaher Business System which makes everything possible.The Senior Supplier Quality Engineer for Cytiva is responsible to manage supplier defects, be… more
- Aldevron (Miami, FL)
- …to regulatory agency inspections or other types of audits (eg, FDA, notified bodies, ISO , etc.).Current or past Quality certifications a plus (eg ISO ... and delivery of solutions that safeguard and improve human health.The Sr. Client Quality Manager is responsible for overseeing all duties related to the Quality… more
- Cytiva (Miami, FL)
- …roles in QA, Operations, or Quality Engineering preferred.Regulatory and Quality Expertise: Strong knowledge of ISO standards, FDA regulations, cGMPs, ... Business System, which makes everything possible.As the Senior Manager, Site Quality you will collaborate closely with cross functional leadership and associates… more
- Cytiva (Miami, FL)
- …manufacturing or medical device production.2+ years experience with regulatory standards and quality systems (eg, FDA, ISO 13485, Good Manufacturing Practices - ... manufacturing processes, managing projects, and ensuring the efficient production of high- quality medical devices and products in a regulated environment. The ideal… more
- Cytiva (Miami, FL)
- …in engineering, Health Sciences, or a related field.Minimum 5 years of experience in Quality or Regulatory in a regulated industry ( ISO 9001, medical device, or ... experience in:Experience in a regulated environment such as medical devices ( ISO 13485), pharmaceuticals (GMP), or biotechnology.Proficiency with quality … more
- Pall (Miami, FL)
- …science fields with 15 years of progressive Regulatory compliance and / or quality assurance experience.Thorough understanding of ISO 9001 and AS9100 / CAA ... Pall is there, helping protect critical operating assets, improve product quality , minimize emissions and waste, and safeguard health. For the exponentially… more
- Beckman Coulter Diagnostics (Miami, FL)
- …world's biggest health challenges. The Senior Staff Global Process Owner (GPO) Quality Assurance for Beckman Coulter Diagnostics is responsible to oversee the ... Corrective and Preventive Action (CAPA) process into our global Quality Management System (QMS) in all aspects of the...standards such as FDA QSR, MDD, CMDCAS, SFDA, JPAL, ISO 13485, ISO 14971 and other applicable… more
- Integrated DNA Technologies (IDT) (Miami, FL)
- …of solutions that safeguard and improve human health.This position is part of the Quality Assurance Department located in Coralville, IA and will be on-site. At IDT, ... improvement of product safety +compliance by effectively managing and resolving quality complaints Communicate with internal team members and external customers to… more
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