| Job alert | Jobs 61 - 70 of 491 |
QC Manager
Xseer Pharmaceuticals
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Los Angeles, CA
... Manager Quality Control Xseer Pharmaceuticals, an FDA licensed outsourcing pharmaceutical 503B is seeking a full-time on-site QC Sr. Manager for our manufacturing facility located in Los Angeles, CA. The QC Manager will be responsible for developing ... - Jun 04
Vice President of Quality
Astrix
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Chino, CA, 91708
... addition to selection, evaluation, and progressive discipline Maintain the customer complaint file Respond and correct all FDA deficiencies Maintain the OTC Master Drug List Interact with all customers, suppliers and regulatory agencies pertaining ... - May 31
Compliance Analyst
Planet DDS
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Irvine, CA, 92606
... specific to relevant regulations and frameworks for our business, including SOC2/Trust Services Criteria for emphasizing security, availability, confidentiality, and privacy, HIPAA Security and Privacy, and ISO 13485/FDA Medical Device compliance. ... - Jun 15
Chemist
Element Materials Technology
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Santa Fe Springs, CA
... Assist in audit preparedness and for participating in quality audits with FDA, other Regulatory Agencies, and customers, as needed Ensures work is in compliance with all state and federal regulations, including but not limited to GMP, DEA, FDA, etc. ... - Jun 06
Quality Manager
Viant
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Upland, CA
$130,000-$150,000 annual
... Position Requirements: Ensure appropriate procedures and policies are implemented to demonstrate compliance to FDA Quality System Regulations (Title 21, CFR, part 820) and other regulatory requirements. Ensure appropriate procedures and policies are ... - Jun 15
Clinical Research Coordinator
UCLA Health
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Los Angeles, CA
... The role requires maintaining all necessary documentation in accordance with FDA regulations, Good Clinical Practice (GCP) guidelines, and the funding source. This includes managing patient registration, data, and treatment assignment. This role ... - May 20
Quality Operations Specialist 1
Source One Technical Solutions
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Irvine, CA
... -Knowledgeable of FDA regulations, 21 CFR part 820 and Part 803 and ISO 13485 standard. -SAP preferred, but not required. Major Accountabilities: -Review and investigate assigned technical and clinical customer complaints. Perform technical ... - Jun 02
IT Analyst
Sapta Global Inc
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Signal Hill, CA, 90755
... disposition.Assists with Document Control and other QA functions.Coordinates and assist in timely review of documentation associated with manufacturing at CMO site.Assists with preparation for FDA and other regulatory agency audits and inspections. ... - Jun 08
Clinical Research Associate I - Cheng Lab, Heart Institute
CEDARS-SINAI
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Los Angeles, CA, 90071
... This role will comply with all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care. Job Duties and Responsibilities: Works with a Clinical Research Coordinator, Research Program Administrator or ... - Jun 17
Sr. QC Analyst
BioPhase Solutions
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Los Angeles, CA
... Plate Readers, Flow Cytometry, PCR, and HPLC Knowledge of cGMP, FDA, and USP regulations and a basic understanding of statistics Knowledge of MS Word and Excel Please send resumes to and visit our website at for additional job opportunities! - May 26