- Abbott (Sylmar, CA)
- …Electrical/Computer Engineering + Software Quality Engineering experience + Prior medical device experience preferred. + Knowledge of Cybersecurity and Data ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Hologic (San Diego, CA)
- …Auditing or similar roles + Clean driver's license + Proficient knowledge of Medical Device Regulations, In Vitro Diagnostic Regulation, cGMP, CFR 820, ... auditing program, ensuring that our suppliers adhere to rigorous regulatory and quality standards. You will lead...part of our mission to deliver safe and effective medical devices that enhance patient outcomes. **Key Responsibilities** +… more
- Danaher Corporation (Brea, CA)
- …would be a plus if you also possess : + Experience in FDA-regulated or medical device manufacturing environments. + Certifications such as CQE, CQA, Six Sigma, ... qualifications, and ongoing performance assessments to ensure adherence to internal quality standards, customer requirements, and applicable external regulatory … more
- Envista Holdings Corporation (Pomona, CA)
- …related field; Master's degree preferred + 5+ years of experience in Engineering; medical device or similar regulated industry highly preferred + Strong ... working closely with cross-functional teams to develop, implement, and maintain quality assurance protocols that comply with regulatory requirements and… more
- BD (Becton, Dickinson and Company) (Milpitas, CA)
- …planning for marketing collateral to support clinical products + Ownership of on-time quality assessments, medical device reporting and health risk ... bodies + Provide subject matter expertise into design of clinical trials for medical device development and submission to the FDA and other regulatory… more
- Abbott (Alameda, CA)
- …10 yrs of work experience will be considered. + Min 10 years of experience in the medical device industry + Min 8 years auditing per ISO and/or FDA standards. + ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- J&J Family of Companies (Irvine, CA)
- …leading Medical /Clinical/R&D teams in a regulated, commercial biomedical or medical device business is strongly preferred 9.) Demonstrated success in ... needs and global standards of care to deliver quality products/solutions. The Director - Medical Affairs...partners including but not limited to R&D, Clinical Research, Regulatory Affairs, Quality & Compliance, Health Economics… more
- Danaher Corporation (Sunnyvale, CA)
- …Union In Vitro Diagnostic Regulation (IVDR) as well as other applicable global regulatory requirements, including Medical Device Single Audit Program (MDSAP) ... Business System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Senior Quality Systems Specialist is responsible for functioning as Lead… more
- Kelly Services (Sacramento, CA)
- …your career, join us as we pioneer progress in the biotechnology and medical device industries. **Workplace:** Onsite in Sacramento, CA. **Position Title:** ... standards. You will ensure compliance with cGMP, GLP, and regulatory benchmarks, protect product quality , and champion...at $25.0 per hour. + Annual bonus eligibility. + Medical , dental, vision coverage, paid time off, and 401k… more
- Astrix Technology (Irvine, CA)
- …for medical devices (eg MDRs, Vigilance reports, etc.) + Familiarity with medical device complaint files and quality records + Knowledgeable of ... - 05/02/2025 Apply for Job Our client is a Medical Manufacturing company enhancing vision and improving quality...and standards, including FDA, ISO 13485, and other worldwide regulatory agencies pertaining to medical devices **Minimum… more