- Astrix Technology (Pomona, CA)
- …personal care products comply with industry regulations and standards, such as FDA guidelines, and work towards continuous improvement in meeting these requirements. ... + Collaborate with production and quality teams to identify areas for process improvement and implement corrective actions to prevent defects and non-conformities. +… more
- Astrix Technology (Pomona, CA)
- …personal care products comply with industry regulations and standards, such as FDA guidelines, and work towards continuous improvement in meeting these requirements. ... + Collaborate with production and quality teams to identify areas for process improvement and implement corrective actions to prevent defects and non-conformities. +… more
- Fujifilm (Sacramento, CA)
- …always prepared to promote and provide reference for our solution, and that the process for utilizing is well defined and organized. + Collaborates closely with MI ... with marketing communications and sales leadership. + Work collaboratively with training manager to ensure all level of sales are prepared to effectively execute… more
- Stanford University (Stanford, CA)
- …and work under close direction of the principal investigator and/or manager /supervisor. The CRCA will support federal and non-federal clinical research studies ... protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices. +… more
- Mentor Technical Group (Millbrae, CA)
- …provides a comprehensive portfolio of technical support and solutions for the FDA -regulated industry. As a world leader in life science engineering and technical ... job-skill deficiencies. + Manages the employee's Time Keeping equipment/software function process . + Requisition materials and supplies, such as tools, equipment,… more
- Astrix Technology (Pomona, CA)
- …personal care products comply with industry regulations and standards, such as FDA guidelines, and work towards continuous improvement in meeting these requirements. ... + Collaborate with production and quality teams to identify areas for process improvement and implement corrective actions to prevent defects and non-conformities. +… more
- Fujifilm (Sacramento, CA)
- …opinion leaders in the Endoscopy space. The role of the Business Development Manager is to understand and define our internal and external endoscopic customers' ... + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and all… more
- Abbott (Sylmar, CA)
- …Work On** + Collaborate with site EHS team and enterprise environmental manager , handle and lead environmental compliance activities, programs and prevention efforts ... directed + On call for EHS emergencies (24/7) + Support ISO 14001 process and its maintenance + Selects and applies environmental management principles, theories and… more
- Danaher Corporation (Sunnyvale, CA)
- …Analyst, Post-Market Surveillance is responsible for managing the adverse event process for Cepheid. This includes assessing complaints cross functionally for ... Quality related functions. This position reports to the Sr. Manager Regulatory Compliance and Post Market Surveillance and is...GMP and QSR requirements for medical devices. (ISO 13485, FDA 's QSRs, EU's MDD, Canadian Regulations) is required. +… more
- BD (Becton, Dickinson and Company) (Brea, CA)
- …allocation, and administration. + Support the Corrective and Preventive Action (CAPA) process . + Lead a team of Quality Managers and Engineers, operating with ... staff. * Deep knowledge of global medical device regulations ( FDA , EU MDR, etc.). * ASQ certification (Engineer or..., EU MDR, etc.). * ASQ certification (Engineer or Manager ) preferred. * Six Sigma Green Belt or Black… more