- AbbVie (Irvine, CA)
- …computerized systems, used within the R&D laboratory function associated with FDA Good Manufacturing Practices (GMP) testing for biological and small molecule ... projects. + Responsible for the planning, design and implementation of validation projects, coordination of validation activities, and preparation of validation documentation within Pharmaceutical Development, with established guidelines for pharmaceutical… more
- Abbott (Santa Clara, CA)
- …You'll Work On** + Prepares robust regulatory applications (either for FDA or for international regulatory agencies) to achieve departmental and organizational ... and adhere to applicable regulatory standards including those set by the FDA or other worldwide regulatory agencies to various international affiliates. + Maintains… more
- Abbott (Milpitas, CA)
- …development, and validation of software for embedded systems, ensuring compliance with FDA requirements. They play a crucial role in software design, coding, and ... activities under guidance and mentoring junior engineers. Adherence to FDA -compliant Design Control procedures and proficiency in software implementation are… more
- VTI Life Sciences (San Diego, CA)
- …environments are validated in compliance with industry standards, regulatory requirements (such as FDA 21 CFR Part 11 and 820, Data Integrity, ISO 13485 and GAMP ... attendance and project coordination. + Provide all services in accordance with FDA cGxP guidelines and regulations. QUALIFICATIONS: + Bachelor's degree or higher in… more
- UCLA Fielding School of Public Health (Los Angeles, CA)
- …Qualifications: * Experience working with radiopharmaceuticals and knowledge of FDA regulatory pathways. * ACRP certification, expertise in regulatory affairs ... and regulatory submissions, IND filings, engagement with the FDA , IRB submissions, GCP, and CITI * Strong relationships...is requesting reference letters and will factor in the quality of these references when assessing the candidate. Apply… more
- Abbott (Alameda, CA)
- …development, and validation of software for embedded systems, ensuring compliance with FDA requirements. They play a crucial role in software design, coding, and ... activities under guidance and mentoring junior engineers. Adherence to FDA -compliant Design Control procedures and proficiency in software implementation are… more
- Charles River Laboratories (Northridge, CA)
- …to quality standards and relevant regulatory requirements (eg, GxP, FDA , ISO) **Job Qualifications** + Bachelor's degree in life sciences, bioengineering, or ... positive impact on the world by providing the highest quality cellular material and services to biotech and pharmaceutical...drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. At Cell Solutions,… more
- Astrix Technology (Gardena, CA)
- …Pay Rate High: 25 + Added - 13/08/2025 Apply for Job ** Quality Assurance Documentation Coordinator** **Position Overview** We are seeking a detail-oriented ... Documentation Coordinator to join our quality assurance team. This role is critical in maintaining...and compliance with established protocols. + Support compliance with FDA , SQF, and other regulatory body requirements. + Ensure… more
- Abbott (Milpitas, CA)
- …the development, verification, ensuring timely delivery and adherence to FDA -compliant design control procedures. They provide technical leadership, mentoring, and ... and implement process improvements. Collaborating with cross-functional teams, they ensure high- quality software delivery and contribute to the full development life… more
- Biomat USA, Inc. (Upland, CA)
- …donor center when the Center Manager is not present. + Collaborates with Training and Quality staff to ensure that training and quality goals are met. + Coaches ... in budget preparation and oversees facility to achieve production targets and quality goals at the agreed-upon cost structure. + Actively delegates, monitors, and… more