- J&J Family of Companies (Irvine, CA)
- …in providing therapeutic and clinical expertise in support of the development of medical devices for the treatment of arrhythmias and structural heart disease. ... leading Medical /Clinical/R&D teams in a regulated, commercial biomedical or medical device business is strongly preferred 9.) Demonstrated success in… more
- Abbott (Sylmar, CA)
- …US and non-US Quality System Requirements and other relevant regulations for medical devices . Previous experience with regulatory body. Knowledge of ... of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines....+ Industry certification preferred. + Class III or II medical device experience. + 3-5 years in… more
- Actalent (Irvine, CA)
- …for supporting electrode product and process sustaining activities through the application of Quality engineering skills for medical devices . Focuses on ... in Engineering or technical discipline required + 5 Years medical device experience required Knowledge, Skills and...13485, ISO 14971, IEC 62304 and FDA QSR for Medical Devices + Ability to work in… more
- J&J Family of Companies (Santa Clara, CA)
- …software development, software verification and validation. + 4 years' experience in a quality role within the medical device , aerospace/defense or similarly ... quality and reliability ensuring the implementation of cutting-edge technology for medical devices is safe, effective, and compliant with regulations,… more
- Astrix Technology (Irvine, CA)
- …external requirements and standards, including FDA, ISO 13485, and other worldwide regulatory agencies pertaining to medical devices **Minimum ... Science + Years' Experience: 0-1 years + Familiarity with regulatory reporting requirements for medical devices... (eg MDRs, Vigilance reports, etc.) + Familiarity with medical device complaint files and quality… more
- Abbott (Sylmar, CA)
- …Electrical/Computer Engineering + Software Quality Engineering experience + Prior medical device experience preferred. + Knowledge of Cybersecurity and Data ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- Hologic (San Diego, CA)
- …compliance. Be a part of our mission to deliver safe and effective medical devices that enhance patient outcomes. **Key Responsibilities** + **Audit Coordination ... auditing program, ensuring that our suppliers adhere to rigorous regulatory and quality standards. You will lead...of 8 years in a regulated industry such as medical devices or pharmaceuticals (required) + 4-5+… more
- Abbott (Santa Clara, CA)
- …meet the existing and emerging regulatory requirements, particularly the EU Medical Device Regulations (EU MDR) and ISO 10993 series. **Principal ... 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 ... work efficiently under tight timelines. **Preferred** + 5+ years prior medical device experience preferred. Apply Now (https://www.jobs.abbott/us/en) **Learn… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …degree and 15+ years of experience in a FDA regulated pharmaceutical and/or medical device industry environment + Strong knowledge of current global Good ... an experienced and dynamic Executive Director of R&D Global Quality to join our team. This pivotal role will...Previous experience of working in the global pharmaceutical and medical device industry. + Experience working with… more
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