Fda Regulations Jobs in San Diego, CA

For further inquiries regarding the following opportunity please contact our Talent Specialist: Meghna at Title: Systems Engineer 3 Location: San Diego CA Duration: 5 months Job Description : Must Haves: 1. Configuration Management Expertise: Proven understanding and More...

As a Clinical Research Physician you will provide clinical mentorship and leadership for clinical development and clinical trials conduct within our organization. You will operate in a wide range of aspects in clinical and pharmaceutical medicine and with patients health authorities c More...

For further inquiries regarding the following opportunity please contact our Talent Specialist: Infant at Title: R&D Portfolio Manager Location: San Diego CA Duration: 9 Months (with possible extension) Remote Workplace: Your location will be a home office; you are not require More...

Description: Must meet all requirements for Clinical Project Assistant position and have demonstrated proficiency in all relevant areas. Provides administrative assistance in site selection study implementation and ongoing coordination of study sites either directly or via CROs. Moni More...

The SubInvestigator provides oversight in medical and clinical issues as requested or required. The SubInvestigator works with the Principal Investigator (PI) to evaluate clinical trials and ensure that all studyrelated procedures are completed in accordance with Good Clinical Practic More...

The SubInvestigator provides oversight in medical and clinical issues as requested or required. The SubInvestigator works with the Principal Investigator (PI) to evaluate clinical trials and ensure that all studyrelated procedures are completed in accordance with Good Clinical Practic More...

The SubInvestigator provides oversight in medical and clinical issues as requested or required. The SubInvestigator works with the Principal Investigator (PI) to evaluate clinical trials and ensure that all studyrelated procedures are completed in accordance with Good Clinical Practic More...

The SubInvestigator provides oversight in medical and clinical issues as requested or required. The SubInvestigator works with the Principal Investigator (PI) to evaluate clinical trials and ensure that all studyrelated procedures are completed in accordance with Good Clinical Practic More...

The SubInvestigator provides oversight in medical and clinical issues as requested or required. The SubInvestigator works with the Principal Investigator (PI) to evaluate clinical trials and ensure that all studyrelated procedures are completed in accordance with Good Clinical Practic More...

The SubInvestigator provides oversight in medical and clinical issues as requested or required. The SubInvestigator works with the Principal Investigator (PI) to evaluate clinical trials and ensure that all studyrelated procedures are completed in accordance with Good Clinical Practic More...

The SubInvestigator provides oversight in medical and clinical issues as requested or required. The SubInvestigator works with the Principal Investigator (PI) to evaluate clinical trials and ensure that all studyrelated procedures are completed in accordance with Good Clinical Practic More...

Resource Management and Training:Participation in QM resource allocationResource allocation of QA auditorsFacilitation of professional development and career advancement of Quality Management staffAdministrative supervision of Quality Management staff jointly with Senior Director Qual More...

The Quality Assurance Specialist will be responsible for routinely reviewing analysis reports to ensure their accuracy completeness and compliance with internal/external guidelines.  As part of this review candidates will identify/initiate CAPAs Deviations Change Controls Process More...

Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients worldwide. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The com More...

Description: Job Title: Clinical Trials Management Associate II Location: Foster City CA Duration: 06 months with possible extension Shift Details: 1st shift/ Monday Friday 8am5pm/business hours Essential Duties and Responsibilities Leads or manage components of Phase I II More...

Description: Bill rate $65$70 depends on experience 100% onsite 5 days a week Job Summary Validation QE II and SR QE(Validation) : As directed by the Quality Engineering Leader the Quality Engineer II is accountable validation execution for manufacturing equipment and support in p More...

Description: JOB SUMMARY Hybrid 4 days on site Bill rate $60 $65 12 years experience The Sr. Specialist Post Market Quality position reports directly to the Director Post Market Quality Field Action. The Sr. Specialist Post Market Quality position is responsible for working with M More...

This Position is Contingent on Contract Award. This position is in support of a proposed repatriation initiative.  The purpose of the facilities is to provide comprehensive care for migrant individuals who are awaiting reunification or repatriation.  This care will begi More...

Senior (Lead) Microbiologist PositionWorking with management leads the daily operations of the Microbiology department ensuring all activities comply with regulatory standards.Implement and maintain GLP and GMP standards throughout all areas of testingUnder the supervision of and in c More...

About This Role The Senior Manager GCP Quality Assurance & Governance in R&D Quality and Compliance provides global strategic leadership for quality and oversight of quality activities in Biogen R&Ds ongoing clinical research and development processes and programs partneri More...