- Kelly Services (Irvine, CA)
- …medical device regulations and standards: 21 CFR Part 820 QSR, ISO 13485, Brazil GMP , Canada Medical Devices Regulations SOR 98-282, Japan's MHLW MO 169, EU MDR ... 2017/745 * Lead Auditor certification from an accredited / recognized organization (preferred)...RESPONSIBILITIES: * Assures that Quality System Audits comply with QSR/ GMP and ISO requirements. * Conducts internal audits of… more
- Catalent Pharma Solutions (San Diego, CA)
- …Prior Supplier Auditing experience and experience in writing supplier audit reports, certified auditor or lead auditor credentials are preferred + Experience and ... sound knowledge of GMP /GDP/GCP regulations, especially those related to comparator sourcing, wholesaler licensing, third party storage and distribution preferred +… more
- LGC Group (Petaluma, CA)
- …Change Control, Audits, CAPAs, Deviations, and QA reporting and approval of GMP documentation. + Quality Operations: Support the following quality processes: Change ... Control, Audits, CAPAs, Deviations, and QA reporting and approval of GMP documentation + Other Duties as mandated by site priorities and Quality, Business, or Safety… more
- Lactalis American Group Inc. (Turlock, CA)
- …the Quality Management System in alignment with quality standards (ISO 22000 and GMP ) and relevant regulations. + Performing regular audits to ensure compliance with ... Microsoft Office. + Professional Certifications Preferred: PCQI, HACCP, and Internal Auditor Certification Skills / Abilities + Strong communication abilities both… more