- Integra LifeSciences (Irvine, CA)
- …for a Medical Device or a highly regulated organization + 3+ years of experience in document management or using an electronic document management system ... PLM Systems. + Support in the preparation, participate, and address issues related to document and change management for internal and external (FDA, BSI, etc.)… more
- AbbVie (Irvine, CA)
- …combination products and biologics. Specific areas of support may include the Document Center, Device QA, Labeling, Validation, Training and CAPA. This position will ... conformance with AbbVie Quality System requirements and all applicable regulatory requirements. *Supplier oversight, assuring responsible Third Parties are complaint… more
- Owens & Minor (Riverside, CA)
- …distribution of USP Medical Oxygen Cylinders. * Oversee and or Conducts Internal Regulatory Compliance Auditing. Team Management * Supervise and support the ... company policies, improving operational performance and compliance with safety, regulatory , quality standards, and resolving customer and operational issues… more
- Adecco US, Inc. (Cupertino, CA)
- …requirements + Experience with quality systems including design change control and document management + Excellent technical writing and communication skills + ... in medical device labelling and a solid understanding of domestic and international regulatory requirements, including 21 CFR 801 and EU MDR. This role requires… more
- City National Bank (Los Angeles, CA)
- … to identify, recommend and effect process changes regarding credit risk management activities, regulatory issues related to credit risk, credit policy, ... Identifies, recommends and effects process changes as related to credit risk management activities, regulatory statutes, credit policy and general credit… more
- Safran (Irvine, CA)
- …and processes in accordance with ARP-4754A and other applicable industry and regulatory standards. The AQE ensures effective implementation of the program plan and ... full compliance of customer, regulatory and company requirements, to achieve company business objectives on all activities performed by the engineering organization.… more
- Adecco US, Inc. (Shafter, CA)
- …closely with the QA Manager to ensure the company meets all internal, regulatory , and customer requirements. This role is responsible for supporting the department's ... + **Audits & Compliance:** Assist with all food safety and regulatory audits, including preparation, on-site support for inspectors, and managing follow-ups… more
- Danaher Corporation (Sunnyvale, CA)
- …for functioning as Lead Internal Auditor to schedule, plan, perform, and document internal audits of Cepheid's Quality Management System (QMS), providing ... opportunity to: + Function as Lead Auditor to schedule, plan, perform, and document internal audits to provide continuous and rigorous assessment of the Cepheid QMS… more
- Gilead Sciences, Inc. (Foster City, CA)
- …the **Sr. Manager, Biostatistics** you will lead biostatistical analysis and reporting, document review and data inclusion for NDA submissions of assigned studies by ... input into clinical development documentation, scientific publications and presentations, and regulatory filings. Dependent upon the area of assignment, you may lead… more
- Abbott (Temecula, CA)
- … and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements. + Complies with US ... root-cause analysis investigation & resolution activities + Lead Risk Management activities from product Concept through Commercialization + Lead design… more