- ThermoFisher Scientific (Fremont, CA)
- …compliance for medical devices or diagnostics. + Strong technical skills in FDA , GMP, ISO 13485 compliance , process improvement, and development. + ... current good manufacturing practices (cGMP) with the highest level of quality and compliance in a safe and timely manner that will meet customer expectations. Works… more
- Kelly Services (Yorba Linda, CA)
- …in Yorba Linda. This is a temporary role focused on ensuring Nobel Biocare's compliance with FDA QSR regulations and ISO 13485 standards through Receiving ... visual aids, specifications, work orders, and engineering drawings to ensure compliance . + Conduct first article inspections on incoming products. + Identify… more
- Compass Group, North America (San Mateo, CA)
- …and policies to develop and provide nutrition resources and to ensure compliance with FDA nutrition labeling laws. **Key Responsibilities:** + Assesses ... and the region. + Monitors, assesses and increases Webtrition usage and compliance within assigned accounts; holds units in region accountable for using Webtrition… more
- Abbott (Milpitas, CA)
- …+ Monitors and ensures compliance with company policies and procedures (eg compliance with FDA regulations, etc.) + *Makes and executes operational decisions ... with a strategic perspective + Directs and controls the activities and budget of one or more functional areas, product groups and/or third party vendors. **QUALIFICATIONS:** + Bachelor's or MS degree in Human Factors Engineering, Biomedical Engineering,… more
- Stryker (Irvine, CA)
- …implement CAPAs for process-related issues. + Document processes, validations, and risk assessments in compliance with FDA 21 CFR Part 820, ISO 13485, and ISO ... 25539 (vascular implants). **What you need:** Required Qualifications: + Bachelor's degree in Engineering (Mechanical or Biomedical preferred) + 2+ years of work experience Preferred Qualifications: + Experience in process development/manufacturing engineering… more
- WuXi AppTec (San Diego, CA)
- …to optimize existing processes (Process R&D); Perform job-specific tasks in compliance with FDA regulations, Safety Consciousness, internal standards, company ... policies, and standard operating procedures (SOPs). **Responsibilities** Must have a Ph.D. in Chemistry or Biochemistry plus 1 year experience in job offered. Require skills and knowledge in Process R&D, Scale up (multi-kg scale), Chromatographic/Analytical… more
- Compass Group, North America (San Francisco, CA)
- …policies to implement wellness related programs and initiatives and to ensure compliance with FDA nutrition labeling laws. **Key Responsibilities:** + ... Understands and executes Bon Appetit's food philosophy and wellness programs including Company wellness commitments and op-in wellness offerings. + Supports account in meeting nutrition related regulatory requirements including federal menu labeling laws,… more
- AbbVie (Irvine, CA)
- …communication skills. Additional 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… more
- AbbVie (Pleasanton, CA)
- …communication skills. Additional 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… more
- Abbott (Alameda, CA)
- …policies and procedures. + Develops and maintains departmental operating procedures to ensure compliance to relevant FDA QSR, ISO guidelines, including 21 CFR ... the Quality System are developed, validated and maintained in compliance with regulatory and corporate requirements. This is an...Quality Assurance. + Knowledge of medical device standards including FDA QSR, ISO 13485, ISO 14971, 21 CFR Part… more