- Kelly Services (Irvine, CA)
- …_Ability to communicate effectively, both in writing and verball_ + _Familiarity with quality and regulatory systems including FDA 's Quality System ... The company partners with clinicians to develop innovative technologies that improve the quality of care for arrhythmia patients worldwide_ _As a Kelly employee, you… more
- AbbVie (Irvine, CA)
- …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 equal opportunity employer… more
- AbbVie (Pleasanton, CA)
- …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 local law: + The… more
- Abbott (Temecula, CA)
- …Minimum 5 years Previous Quality engineering experience and demonstrated use of Quality tools/methodologies. Detailed knowledge of FDA , GMP, and ISO 13485 + ... diversity, working mothers, female executives, and scientists. **The Opportunity** **The Sr, Quality Engineer position works onsite of our Temecula, CA location in… more
- Amgen (Thousand Oaks, CA)
- …priorities in a very dynamic environment + Experience in project management and FDA type Quality Management Systems + Ability to lead projects independently ... of thermal packaging systems, packaging engineering, material science, and/or transportation- quality systems + Experience in conducting technical assessments with… more
- Medtronic (San Francisco, CA)
- …additional overnight or occasional flight travel. + Understands and adheres to FDA Regulations, quality and training requirements, SOPs, and Work ... Instructions-continually looking for opportunities to improve quality . + Stay current on internal training requirements and...needs. + Proven ability to produce consistent, detail oriented, high- quality work. + Ability to make sound decisions and… more
- ABM Industries (Carlsbad, CA)
- …policies. + Demonstrates commitment to the development, implementation and effectiveness of Quality Management System per ISO, FDA , and other regulatory ... agencies. + Understands and is aware of the quality consequences which may occur from the improper performance...Remain knowledgeable of current federal and international regulations, including FDA 21CFR part 820, FDA 21CFR part… more
- Abbott (Pleasanton, CA)
- …+ 5+ years related work experience + Engineering experience and demonstrated use of Quality tools/methodologies + Detailed knowledge of FDA , GMP, ISO 13485, and ... their lives. We are seeking an experienced, high caliber Senior Supplier Development Quality Engineer to be responsible to act as the site interface to suppliers.… more
- Takeda Pharmaceuticals (Los Angeles, CA)
- …Provide assessments to support good understanding and knowledge of current regulatory requirements ie, FDA , ISO, and Takeda Quality Systems, and serve as a plant ... is true to the best of my knowledge. **Job Description** **Senior Quality Analyst- Nights** **Takeda Pharmaceuticals** **About the Role:** You will perform all… more
- Abbott (Santa Clara, CA)
- …software, cybersecurity, telehealth, etc.) have targeted mitigations to align with FDA expectations, ensuring high- quality submissions and predictability for ... experience such as from the Food and Drug Administration ( FDA ) Center for Devices and Radiological Health (CDRH). This...for new products or changing existing products especially with FDA + Supports and provide critical review of key… more
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