Hospital/ Medical Sales Consultant-Washington DC/ Baltimore |
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Eloquest Healthcare
Hospital/ Medical Sales Consultant – Washington DC/ Baltimore
R... |
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Clinical Research Regional Monitor - East Coast |
| JOB SUMMARY:
Implement and carry out monitoring functions for clinical research studies. S... |
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Clinical Nurse Educator (CNE)/Community Advocacy Manager (CAM) |
| The Therapeutics Institute (TTI) is a division of inVentiv Health, Inc. inVentiv Health Inc. (NASDAQ... |
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Clinical Research Regional Monitor |
| AGA Medical Corporation, a medical technology company, is dedicated to the development, design, ... |
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Business Unit Brand Director - Cell Biology |
| My client is an international biological resource center supporting global scientific research by ... |
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SALES Professionals Needed! All industries INTERVIEW Apr 23rd 3-8PM! |
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Evening Sales Interview Conference from 3:00 PM to 8:00 PM
Washington DC/N... |
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Director of Pharmaceutical Development |
| This position reports to the Chief Scientific Officer, Research andDevelopment. This position is ... |
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Area Sales Manager |
| Company:
Amega Scientific has quickly become the leader in providing Centralized Monitoring ... |
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Regional Account Manager- NIH |
| Innovation is in our genes.
Illumina (NASDAQ: ILMN) develops next-generation tools for large-scale ... |
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Quality Control Analyst I - (Job Number: 0805513)
| Details |
Country: USA
Location: Delaware-Delaware US-DE-Delaware
Total applied: 2 |
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Quality Control Analyst I - (Job Number: 0805513)
Quality Control Analyst I - (Job Number: 0805513) DescriptionNoracmo, Inc., a member of the Johnson & Johnson family of comapnies, currently has an opening for a Quality Control Analyst I at our facility in Wilmington, DE. General Purpose of Job: Under general supervision, conducts chemical and physical laboratory tests and analyzes raw materials, intermediates and final product to ensure compliance with standards. Tests and analyzes raw materials, in-process samples and products such as chemicals and Active Pharmaceutical Ingredients to determine stability, purity, chemical content and other characteristics. Follows standardized formulas and experimental procedures. Legibly documents analysis results in real-time and communicates results to internal customers. Maintains sample control of all samples submitted to the laboratory. Reviews peer laboratory data. Troubleshoots and performs minor maintenance and repair of laboratory instrumentation. Inventories, orders and maintains adequate supply of chemicals and general supplies for QC labs. Assures accurate and timely input of QC data into information systems such as ERP, databases, etc. Assures that QC Labs run in a safe, clean and environmentally sound manner. Maintains detailed records for FDA, DEA and safety and environmental purposes. Associate's Degree (A. A.) and two to four years experience with wet chemistry and/or basic laboratory skills. Working experience in a cGMP/cGLP environment is required. Work experience in a pharmaceutical manufacturing environment is strongly preferred. Read and interpret documents such as safety rules, operating and maintenance instructions, and standard operating procedure manuals. Write routine reports and business correspondence and standard operating procedures manuals. Knowledge of chemical concepts and theories. Familiar with a variety of laboratory equipment, such as: GC, HPLC, Karl Fisher, etc. Successfully completes regulatory and job training requirements. Enter data into computer using software applications for data entry and word processing. Ability to perform repetitive tasks while maintaining speed of work and attention to detail without loss to production. Ability to perform under stress in cases of emergency, critical or hazardous situations. Ability to work with others in a team environment. Apply Now
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