- Beckman Coulter Diagnostics (Miami, FL)
- …that address the world's biggest health challenges. The Senior Staff Global Process Owner (GPO) Quality Assurance for Beckman Coulter Diagnostics is responsible to ... the development, governance and integration of the Corrective and Preventive Action (CAPA) process into our global Quality Management System (QMS) in all aspects of… more
- Cytiva (Miami, FL)
- …a regulated environment. The ideal candidate will have experience in process engineering, project management, and a strong understanding of healthcare manufacturing ... control, and other departments to ensure smooth operations.Develop and maintain process documentation, including standard operating procedures (SOPs), process … more
- Cytiva (Miami, FL)
- …discovery to delivery. What you will do:Supplier qualification, including supplier process qualification (SPQ) for Type I (critical) supplier.Manage the supplier ... corrective actions process (SCAR) and supplier change requests (SCR).Provide input and...a plus if you also possess previous experience in:Medical Device , eg ISO 13485PharmaceuticalChemicalAutomotive, eg IATF 16949Speaking fluent SpanishCytiva,… more
- Beckman Coulter Diagnostics (Chaska, MN)
- …technical environment, focused on innovative test solutions, automation, data analytics, and process improvements and want to work to build a world-class Test ... with the operations teams in support of tester installation qualification, process validation and process improvement activitiesThe essential requirements of… more
- Beckman Coulter Life Sciences (Miami, FL)
- …Risk Management (per ISO 14971), Production, Service Controls. Assuring compliant process and product documentation, inclusive of Design History, Product, Process ... development, manufacturing and / or quality systems (ISO 9001), medical device (ISO 13485), pharmaceutical, related life sciences or other regulated industries.It… more
- Cytiva (Miami, FL)
- …from discovery to delivery.What you will do:Supplier qualification, including supplier process qualification (SPQ) for Type I (critical) supplier.Manage the supplier ... corrective actions process (SCAR) and supplier change requests (SCR).Provide input and...a plus if you also possess previous experience in:Medical Device , eg ISO 13485PharmaceuticalChemicalAutomotive, eg IATF 16949#LI-OnsiteJoin our winning… more
- Cytiva (Miami, FL)
- …& Advocacy: Collaborate with site and global leadership to address process changes, advocate for site-specific needs, and drive customer-centric solutions during ... Engineering, or Manufacturing Operations within Life Sciences, Biotechnology, Medical Device , Biopharma, or other FDA or EPA-regulated manufacturing environments.Possess… more
- Beckman Coulter Diagnostics (Miami, FL)
- …OR Doctoral degree in fieldExperience in software, test method, equipment, process , and/or design testing methodologies.Knowledge of FDA regulations, ISO standards, ... and GxP guidelines.Experience with Computer System Validation (CSV) and process validationIt would be a plus if you also possess previous experience in: Experience… more
- Cytiva (Miami, FL)
- …manufacturing and design, ensuring compliance with regulatory standards and driving process improvements; leading root cause analysis and CAPA initiatives, ensuring ... and Concession Control Boards, ensuring compliance with quality standards.Implement process improvement initiatives using Six Sigma, Lean Manufacturing, DBS and… more
- Raytheon (Mckinney, TX)
- …Windchill and the Common PDM system, ASME BTH-1 (Below-the-Hook Lifting Device Design)Active and transferable DoD Security ClearanceWhat We OfferOur values drive ... agency of the Department of Defense, handles and adjudicates the security clearance process . More information about Security Clearances can be found on the US… more
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