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in Vitro Diagnostics Jobs in California

1 - 15 of 40
1 - 15 of 40
Search Results - in Vitro Diagnostics Jobs in California
CorDx-San Diego
The Quality and Regulatory Compliance Specialist is responsible for ensuring that development processes for all in vitro diagnostic (IVD) products comply with applicable regulatory requirements and quality standards. This role will work closely with cross...
resume-library.com -
Abbott Laboratories-San Diego
years' experience in this area of expertise.  •  OR Bachelor's degree and 6 years' experience in this area of expertise. Preferred Qualifications  •  Eight or more years of experience working in the in vitro diagnostics field in an industrial setting...
Katalyst Healthcares & Life Sciences-Irvine
Responsibilities: Must Have MDR experience. IVD (In-vitro Diagnostics) is highly preferred. Support the IVDR project by revising the assigned technical files. Each technical file must be generated using the latest technical file template...
resume-library.com -
1 similar job: Spring
Abbott Laboratories-Alameda (CA)
Food and Drug Administration 21CFR 820 and 11, US FDA cGMP, 21 CFR 210, 211, and 21CFR Part 4.  •  MDSAP, ISO 9001, ISO 13485, ISO 14971, IEC 62304.  •  In Vitro Diagnostic Medical Device Directive (IVDD) 98/79/EC. Medical Device Regulation (MDR) 2017/745...
Guardant Health-Redwood City
multiple products in multiple different regulatory environments and will become even more so as Guardant moves into further in vitro diagnostic (IVD) development and into cancer screening. Staff Pathologist Essential Duties and Responsibilities...
resume-library.com -
Abbott Laboratories-Pomona
/on-market support of In-Vitro Diagnostics (IVD) medical device products, facilitating the application of design/change controls, risk management, quality plans, and implementation of design and development plans.  •  Assist in the development and execution...
3 similar jobs: Sylmar, Westbrook, Plano
TalentBurst, Inc.-San Rafael (CA)
biomarker operations, vendor management, translational sciences operations, clinical operations. Strong knowledge and understanding of clinical drug development strategic planning of clinical research, ICF, ICH GCP, GLP, In Vitro Diagnostic Regulation (IVDR...
resume-library.com -
Abbott Laboratories-Alameda (CA)
Experienced in regulatory submissions for Pharmaceutical, in vitro diagnostic devices and/or medical devices.  •  Experience of working within the requirements of 21 CFR 820, ISO 13485, the Medical Devices Directive (93/42/EEC) and/or the IVD Directive (98/79/EC...
Katalyst Healthcares & Life Sciences-Pleasanton (CA)
Sciences, Biology (or equivalent vocational qualifications). Experienced in regulatory submissions for Pharmaceutical, in vitro diagnostic devices and/or medical devices. Experience of working within the requirements of 21 CFR 820, ISO 13485, the Medical...
resume-library.com -
Abbott Laboratories-Pleasanton (CA)
in regulatory submissions for Pharmaceutical, In vitro diagnostic devices and/or medical devices.  •  Experience of working within the requirements of 21 CFR 820, ISO 13485, the Medical Devices Directive (93/42/EEC) and/or the IVD Directive (98/79/EC). Preferred...
San Diego
where only limited standardization exists required.  •  Basic knowledge in the use of gauges and other measuring devices preferred.  •  Basic knowledge of quality and quality control principles for in vitro diagnostics manufacturing.  •  Basic knowledge...
icims.com -
Abbott Laboratories-San Diego
years' experience in this area of expertise.  •  OR Bachelor's degree and 6 years' experience in this area of expertise. Preferred Qualifications  •  Eight or more years of experience working in the in vitro diagnostics field in an industrial setting...
jobs.abbott -
Santa Ana
analysis of clinical literature, and evaluating and reviewing clinical data, generated both pre and post-market for medical devices and in vitro diagnostic devices. In addition, the Clinical Affairs Specialist will assist in performing annual activities...
icims.com -
Eurofins-Lancaster
clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins...
smartrecruiters.com -
Amazon-Sunnyvale
Biomedical Engineering, life Sciences, Biology (or equivalent qualifications)  •  · 5-7 years of experience in regulatory submissions for In Vitro Diagnostic Devices, Pharmaceutical and/or Biologics (small molecules & biologics)  •  · 5-7 years of experience working within...
amazon.jobs -
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