- Abbott (Temecula, CA)
- …compliance of the Quality System. (eg compliance with internal procedures and FDA , BSI regulations etc). + Interacts with internal and external customers, by ... meeting regularly, responding to requests and explaining procedures. + Interprets and executes policies that affect work processes and personnel within the assigned organizational unit. + Contributes to the development of operational policies and procedures… more
- AbbVie (Irvine, CA)
- …computerized systems, used within the R&D laboratory function associated with FDA Good Manufacturing Practices (GMP) testing for biological and small molecule ... projects. + Responsible for the planning, design and implementation of validation projects, coordination of validation activities, and preparation of validation documentation within Pharmaceutical Development, with established guidelines for pharmaceutical… more
- Schwan's Company (La Palma, CA)
- …industry standards of quality and food safety, GMPs, HACCP, food labeling and FDA /USDA regulations + General culinary knowledge and passion for global food is ... beneficial Compensation and Benefits: The base salary range for this position is $73,500 to $122,500 annually with eligibility for a 10% annual incentive bonus, that is based on organizational performance. The pay range represents the numerous factors… more
- Abbott (Sylmar, CA)
- …requirements. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, operating procedures, processes, ... and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. + Performs other related duties and responsibilities, on occasion, as assigned. **Required… more
- Terumo Neuro (Aliso Viejo, CA)
- …test method validation and data analysis. 3. Demonstrated command and knowledge of FDA and ISO medical device quality system requirements. 4. Proven experience in ... statistical analysis (statistical analysis tools). 5. Proficient computer skills including MS Word, Excel, and statistical software (eg, MiniTab, Statgraphics, Design of Experiment DOE, etc.). 6. Solid written and verbal communication skills. **Desired… more
- Fujifilm (Sacramento, CA)
- …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... other applicable laws, regulations and standards. + Comply with and pass all requirements for vendor credentialing as part of gaining access to hospitals and facilities to perform assigned job duties. **Qualifications:** + Bachelor's degree in biomedical… more
- AbbVie (Irvine, CA)
- …Requirements: * Responsible for performing all duties in compliance with FDA 's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, ... and all other international regulatory requirements with which ZELTIQ complies. Additional Information All your information will be kept confidential according to EEO guidelines. Salary: $35,000 - $172,500 AbbVie is an equal opportunity employer and is… more
- AbbVie (Pleasanton, CA)
- …Requirements: * Responsible for performing all duties in compliance with FDA 's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, ... and all other international regulatory requirements with which ZELTIQ complies. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: + The compensation range… more
- ZOLL Medical Corporation (Santa Rosa, CA)
- …Super Saturated Oxygen (SSO2) Therapy is the first FDA -approved therapy since the stent 20+ years ago to ... reduce infarct size in patients with the most severe heart attacks. Heart disease is the leading cause of death for both men and women in the US At ZOLL, your work will help to ensure cardiac patients get the life-saving therapy they need.ZOLL has been… more
- Abbott (San Jose, CA)
- …travel plans. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, company policies, operating procedures, processes, ... and task assignments. + Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. + Interacts with customers and assigned institutions, physicians and technicians, customer purchasing… more