| Job alert | Jobs 61 - 70 of 1179 |
Business Objects Developer
COMPQSOFT
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Floris, VA, 20171
... CompQsoft is Certified CMMI Level 3 practitioner for Development and Services, ISO 9001:2015, ISO 27001:2013 & ISO 200001:2011 Certified. CompQsoft is a fast growing company with a strategy and methodology that is strongly focused on the success of ... - May 10
Assistant Director, Business Operations Clinical Research, SMHS
George Washington University
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Washington, DC, 20022
... Comprehensive knowledge of legal and budgetary elements in clinical research contracting with pharmaceutical companies and medical device manufacturers for FDA Direct experience in review of consent forms for FDA regulated clinical research ... - May 06
FR - Database Administrator - II
SoftPathTechnologies
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Sterling, VA, 20146
... Bachelor's degree in related field preferred Thanks and Regards Malleswari Recruitment Contact: Email: SOFTPATH TECHNOLOGIES LLC An ISO 27001: 2013, 9001: 2015, 20000-1: 2018 Certified Company Do follow OUR page for New USA requirements/ Open ... - May 08
Associate Quality Assurance Specialist
ATCC
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Gaithersburg, MD, 20877
... Familiarity with regulatory standards such as ISO 9001, FDA regulations, or other industry-specific quality management systems preferred. Strong analytical and problem-solving skills with a keen attention to detail. Excellent communication and ... - May 10
Risk Manager
Cynet Systems
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Washington, DC
... Proficiency in ISO 13485, ISO 14971, FDA CFR 820, EU 2017/745, IEC 62304, IEC 82304, and IEC/TR 80002-1 standards. Experience in medical device risk analysis, evaluation of risk control measures, and validation testing. Excellent interpersonal ... - May 08
Veterinary Technician
Charles River Laboratories
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Poolesville, MD, 20837
... Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and ... We have proudly supported the development of 86% of the drugs approved by the FDA in 2021. Equal Employment Opportunity ... - Apr 19
Production Operator I - III (Solid Dosage/OSD Manufacturing)
Granules
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Chantilly, VA, 20151
... Key Accountabilities: Operates pharmaceutical production machinery and follows the procedures for manufacturing such as ... Knowledgeable of FDA regulations, GMP, Lean Manufacturing, Six-Sigma, etc. Solid working knowledge and skills in procedures, ... - May 01
Warehouse Coordinator (Temp to perm)
Granules
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Bull Run, VA, 20109
... 1-2 years’ experience in pharmaceutical/food industry. Manufacturing: 2 years (Preferred) cGMP environment: 2 years (Preferred) FDA and OSHA regulations: 2 years (Preferred) - May 02
Clinical Advisor
Axle
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Rockville, MD
... Ensure that pharmaceutical concerns raised during the DCRC and other meetings are addressed in a timely manner. Advise the protocol team regarding pharmaceutical issues relating to DAIT/NIAID standards, FDA and other Health Authorities regulations, ... - May 09
Clinical Advisor
Axle
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Rockville, MD
... Ensure that pharmaceutical concerns raised during the DCRC and other meetings are addressed in a timely manner. Advise the protocol team regarding pharmaceutical issues relating to DAIT/NIAID standards, FDA and other Health Authorities regulations, ... - May 09