FDA Regulations Jobs in USA
FDA Regulations Jobs in USA
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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...
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...
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...
Ability to prepare timely accurate entry declarationsMust be able to meet/exceed our best in class key performance indicators on a daily basisMust be visionary and able to bring ideas to leadership to improve processesOpen files as requiredMonitor timely entry releaseMonitor all More...
The Microbiologist I works independently on assigned Microbiological projects and conducts analyses of raw materials finished products and waters. As a professional scientist the Microbiologist is expected to work under the guidance of supervisors and managers develop skills and under More...
Net Developer With Software As A Medical Device Samd Experience Is Mandatory
Key Responsibilities:Independently execute tasks to upgrade the .NET Framework from 4.7 to 8.0 including analyzing requirements planning and implementing solutions with minimal guidance.Extend and enhance an existing complex software system.Update and enhance APIs and SQL Databases.Us More...
Clinical Research Coordinator
Supports and works closely with the Principal Investigator and Clinical Nurses to administratively coordinate protocol implementation for multiple research studies. CRC conducts dayto day activities of multiple studies with respect to compliance regulatory recruitment study site initi More...
Job Title: MES Architect Location: Bridgewater NJ(Hybrid) Duration: Long Terms Open Rate Job Description Client is looking for a MES Manufacturing Execution System Architect who has a strong understanding of the Biotech / Pharma manufacturing environment. The ideal candidate will have More...
The Microbiologist I works independently on assigned Microbiological projects and conducts analyses of raw materials finished products and waters. As a professional scientist the Microbiologist is expected to work under the guidance of supervisors and managers develop skills and under More...
Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients worldwide. Our client is an American multinational information technology services and consulting company and is a leading prov More...
Job Title: Vet Tech Marketing Coordinator Duluth GA 6 months ( Contract to hire ) Key responsibilities: Assist the Vet Tech Marketing team with administrative support on as needed basis (entering updating and maintaining team and department financials tracking POs invoices contracti More...
Net Developer With Software As A Medical Device Samd Experience Is Mandatory
Key Responsibilities:Independently execute tasks to upgrade the .NET Framework from 4.7 to 8.0 including analyzing requirements planning and implementing solutions with minimal guidance.Extend and enhance an existing complex software system.Update and enhance APIs and SQL Databases.Us More...
Net Developer With Software As A Medical Device Samd Experience Is Mandatory
Key Responsibilities:Independently execute tasks to upgrade the .NET Framework from 4.7 to 8.0 including analyzing requirements planning and implementing solutions with minimal guidance.Extend and enhance an existing complex software system.Update and enhance APIs and SQL Databases.Us More...
Net Developer With Software As A Medical Device Samd Experience Is Mandatory
Key Responsibilities:Independently execute tasks to upgrade the .NET Framework from 4.7 to 8.0 including analyzing requirements planning and implementing solutions with minimal guidance.Extend and enhance an existing complex software system.Update and enhance APIs and SQL Databases.Us More...
Job Title: Vet Tech Marketing Coordinator Duluth GA 6 months ( Contract to hire ) Key responsibilities: Assist the Vet Tech Marketing team with administrative support on as needed basis (entering updating and maintaining team and department financials tracking POs invoices contracti More...
Job Title: Vet Tech Marketing Coordinator Duluth GA 6 months ( Contract to hire ) Key responsibilities: Assist the Vet Tech Marketing team with administrative support on as needed basis (entering updating and maintaining team and department financials tracking POs invoices contracti More...
Net Developer With Software As A Medical Device Samd Experience Is Mandatory
Key Responsibilities:Independently execute tasks to upgrade the .NET Framework from 4.7 to 8.0 including analyzing requirements planning and implementing solutions with minimal guidance.Extend and enhance an existing complex software system.Update and enhance APIs and SQL Databases.Us More...
Net Developer With Software As A Medical Device Samd Experience Is Mandatory
Key Responsibilities:Independently execute tasks to upgrade the .NET Framework from 4.7 to 8.0 including analyzing requirements planning and implementing solutions with minimal guidance.Extend and enhance an existing complex software system.Update and enhance APIs and SQL Databases.Us More...
Clinical Research Coordinator
Supports and works closely with the Principal Investigator and Clinical Nurses to administratively coordinate protocol implementation for multiple research studies. CRC conducts dayto day activities of multiple studies with respect to compliance regulatory recruitment study site initi More...
Manufacturing Quality Engineer main purpose is to ensure that all manufacturing processes are in control and conforming to Eurofins Genomics process specification that then deliver products that meet aligned upon customer requirements.Overall Objectives and Responsibilities:Root Cause More...
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