FDA Jobs in USA

Below mentioned is the job description for your reference: Job Title: Operator 2 Machine Duration: 12 months Location: Hunt Valley MD USA 21031 Shift Time: 3rd shift 10pm 6:30am Description: Must have prescreening form and machine operation experience Must have a high school dip More...

Pay rate is $22.05 per hour.Repete Operation.Complying with all OSHA Regulations.Comply FDA GMP.Weekly inventory of raw ingredients and finished feed.Track Mobile and Fork Lift operation after training.Other duties as assigned.We offer our TEAM Members the following benefits:Medical d More...

Job Description: Seeking a fulltime Roadway Design Engineer to join our Maitland office. The ideal candidate will demonstrate a commitment to customer satisfaction accountability and selfmanagement. Strong communication skills a collaborative spirit and a goaloriented mindset More...

Description: As a Manufacturing Laboratory Technician I you will be responsible for: Execution of instructions to manufacture chemical and biological reagents Record and audit information (e.g. batch records log book) Analyze data against predetermined requirements Calibr 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 Quality Management System (QMS) Specialist will be responsible for developing implementing maintaining and improving the companys Quality Management System (QMS). This role ensures that the QMS is compliant with ISO 13485 ISO 9001 21 CFR 820 and 21 CFR 58. The QMS Specialist will More...

General SummaryUnder limited supervision and with the latitude for initiative and independent judgment performs coordinates and manages the creation and outsourcing of billing analysis in accordance with the Center for Medicaid and Medicare Services (CMS) regulations and the More...

The Quality Management System (QMS) Specialist will be responsible for developing implementing maintaining and improving the companys Quality Management System (QMS). This role ensures that the QMS is compliant with ISO 13485 ISO 9001 21 CFR 820 and 21 CFR 58. The QMS Specialist will More...

Applies GMP/GLP in all areas of responsibility as appropriateMonitor laboratory compliance with respect to expired reagents reagent labeling lab cleanliness training records PPE adherence and other cGXP items as needed to help minimize laboratory audit findings.Perform/Support Interna More...

General SummaryUnder limited supervision and with the latitude for initiative and independent judgment performs coordinates and manages the creation and outsourcing of billing analysis in accordance with the Center for Medicaid and Medicare Services (CMS) regulations and the 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...

Applies GMP/GLP in all areas of responsibility as appropriateMonitor laboratory compliance with respect to expired reagents reagent labeling lab cleanliness training records PPE adherence and other cGXP items as needed to help minimize laboratory audit findings.Perform/Support Interna More...

This is a remote position.Summary:The Clinical and Medical Affairs Administrator is a key role supporting the Clinical and Medical Affairs department focusing on contract execution budget oversight and operational support. This position ensures smooth coordination between Legal Fin More...

The entry level position is designed to train the new technician on one of the four (4) analytical aisles in the QC laboratory. In this role they will prepare process and/or finished product samples; perform analytical testing using instrumental and wet chemistry procedures and record More...

Job Description: We are seeking an experienced MES Implementation Project Manager with a strong background in Medical Device regulations and manufacturing systems to lead and drive the successful deployment of Manufacturing Execution Systems (MES) in a regulated environment. The ideal More...

Job Title: Electrical Hardware Engineer Medical Device Location: Raleigh NC (Onsite) Contract: 12 Months Visa Status: Preferably GC USC H4EAD and local Job Description: Essential Duties and Responsibilities Other duties may be assigned: Identifies and develops n 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...