- Philips (Ontario, CA)
- …areas. The role is site based in Ontario, CA - an air-conditioned FDA regulated manufacturing environment for Medical Devices and Pharmaceutical drugs (ISO 13485). ... + Effectively work in a high volume, fast paced FDA regulated manufacturing environment providing safety orientation and trainings...won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work… more
- Abbott (San Diego, CA)
- …identified, obtained, and effectively presented for product registration worldwide (US, FDA , CE-IVDR, PMDA, etc.). **Strategic Planning:** + Identify and approve new ... +7 years of experience in regulatory preferred but may consider quality assurance, research and development/support, scientific affairs, operations, or related area.… more
- Cedars-Sinai (Los Angeles, CA)
- …all federal and local agencies, including the Food and Drug Administration ( FDA ) and local Institutional Review Board. Primary Duties and Responsibilities: + ... interpreting and presenting findings to support study objectives and data quality initiatives. + Identifies and resolves operational/data problems, recommending and… more
- UCLA Fielding School of Public Health (Los Angeles, CA)
- …and preclinical PET biomarkers in compliance with internal procedures, cGMP, other FDA regulations and United States Pharmacopeia standards. The candidate is also ... students the fundamentals of clinical grade radiolabeled biomarker production and FDA compliant procedures and operations. Interested candidates should submit their… more
- BD (Becton, Dickinson and Company) (Milpitas, CA)
- …for marketing collateral to support clinical products + Ownership of on-time quality assessments, medical device reporting and health risk assessments to the ... FDA and other regulatory bodies + Provide subject matter...trials for medical device development and submission to the FDA and other regulatory bodies + Identify and communicate… more
- Abbott (Alameda, CA)
- …development, verification, and validation under guidance. + Adhere to FDA -compliant Design Control procedures for software development. + Demonstrate proficiency ... team members. **Preferred Qualifications** + Knowledge of the principles of quality software engineering as described by software lifecycle development processes… more
- Cedars-Sinai (Los Angeles, CA)
- …all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board (IRB). Primary Duties and Responsibilities + ... meetings. + Notifies direct supervisor about concerns regarding data quality and study conduct. + Works closely with a...and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board. + Maintains research… more
- Gilead Sciences, Inc. (Foster City, CA)
- …aspirations. Join Gilead and help create possible, together. **Job Description** Gilead R&D Quality is a phenomenal place to develop your skills and expertise. Our ... diverse and expert team. We are a committed team of highly skilled Quality professionals dedicated to helping deliver life-saving therapies for unmet needs. We bring… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Description** **Job Responsibilities:** + Lead in the development and implementation of quality strategy and associated capabilities to support the CDS objectives + ... Manage quality review of clinical trial documents, workflows, and outputs...to the conduct of clinical trials and guidelines (eg, FDA , EMA, ICH) and related industry standards and trends… more
- Nestle (Arvin, CA)
- …Position Summary: Ensures incoming finished product compliance with Nestle Quality Systems and Standards and other regulatory governances. Supervises and ... directs the daily activities of the Inventory and Quality Control Technicians by scheduling and assigning workloads, and...or sorting operations. + Assist with external audits by FDA , USDA, etc. INVENTORY CONTROL + Monitor open return/refusal… more