- AbbVie (Irvine, CA)
- …Tok (https://www.tiktok.com/@abbvie) . Job Description AbbVie's Clinical Sciences Development Program - Medical Device consists of three rotations over two years ... identification of internal audit trends, knowledge management, and robust proactive CAPAs. + Medical Device & Combination Products QA (MDCP QA) oversees new… more
- Abbott (Alameda, CA)
- …+ Work closely with in-country regulatory representatives, compile, prepare, and review medical device or IVD submissions to regulatory agencies in the ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- Abbott (Alameda, CA)
- …+ Work closely with in-country regulatory representatives, compile, prepare, and review medical device or IVD submissions to regulatory agencies in the ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- Abbott (Santa Clara, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... existing submissions. + Generate and review documents to support adherence to Medical Device Regulations (MDR) **Required Qualifications:** + Advanced degree in… more
- Aerotek (Irvine, CA)
- …year or 18 months. + As an assembler, you will contribute to the production of medical devices that play a crucial role in healthcare. + All candidates MUST be ... part assembly experience with a microscope. + Experience in medical device assembly and cleanroom environments. +...work culture and the satisfaction of contributing to life-saving medical devices . + Additionally, we provide catered… more
- IQVIA (San Francisco, CA)
- …area guidance for clinical development plans in compliance with applicable regulatory , medical , and ethics guidelines. + Ensure high-quality, data-driven ... leaders, and identifying new business opportunities. + Provide due diligence scientific, medical , regulatory , and drug development expertise and activities for… more
- AbbVie (Pleasanton, CA)
- …with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which ... our talent pipeline and considered for future opportunities. The Device Engineer will work collaboratively with a team to...* Prefer at least three years of experience in medical devices , ideally class II devices… more
- AbbVie (Irvine, CA)
- …with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which ... our talent pipeline and considered for future opportunities. The Device Engineer will work collaboratively with a team to...* Prefer at least three years of experience in medical devices , ideally class II devices… more
- J&J Family of Companies (Santa Clara, CA)
- …is a plus. + Understanding of clinical trial design, GxP principles, and FDA/EMA regulatory requirements, particularly for medical device submissions such as ... aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease...programmer with a strong interest in clinical data analysis, regulatory processes (such as PMA or 510(k) submissions), and… more
- Abbott (Santa Clara, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... potential impact on the business **Preferred** **Qualifications** + Experience in the medical device industry preferred + Experience with clinical trials… more
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