Clinical Data Manager: Successful Mid-Size Biopharma (NY), Flexible Working Environment |
| Clinical Data Manager: Successful Mid-Size Biopharma (NY), Flexible Working Environment
T... |
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MULTIPLE PHARMACEUTICAL SALES OPPORTUNITIES**INTERVIEW IN PERSON APRIL 24 |
| MULTIPLE PHARMACEUTICAL SALES OPPORTUNITIES IN WHITE PLAINS:ELI LILLY, GLAXOSMITHKLINE (GSK) AND SCH... |
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Head VInext 2 (Scientist to Asst Director) |
| Located in the beautiful Hudson Valley region of New York, Regeneron is a biopharmaceutical Company ... |
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Biostatistician 1077 |
| Located in the beautiful Hudson Valley region of New York, Regeneron is a biopharmaceutical Company ... |
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Software Test Engineer |
| Position Overview
Develop and execute software test cases for the Immunodiagnostic P... |
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Documentation Coordinator, Process Technical Services |
| DOCUMENTATION COORDINATOR - PROCESS TECHNICAL SERVICES
Barr Pharmaceuticals, Inc. a holding ... |
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Pharmaceutical Sales Representative-White Plains, NY 2ACF3C |
| Welcome to Novartis - the company that considers its employees to be its greatest asset. Good B... |
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Scientist |
| Welcome to Novartis - the company that considers its employees to be its greatest asset. Good B... |
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R&D Research Investigator/Tech Writer |
| R&D RESEARCH INVESTIGATOR/TECHNICAL WRITER
Barr Pharmaceuticals, Inc. a holding company that ... |
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Formulations Scientist |
| FORMULATION SCIENTIST
Barr Pharmaceuticals, Inc. a holding company, is a global specialty ... |
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Manager/Scientist Downstream Processing and Purification
| Details |
Country: USA
Location: New York-Syracuse Syracuse
Total applied: 15 |
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Manager/Scientist Downstream Processing and Purification
Skills Required: Downstream Processing, Protein Purification, Process Improvement, Process Characterization, Process Validation, Viral Clearance, Chromatography, Filtration, cGMP Manufacturing, DOE - Design Of Experiment Job Description: Manager/Scientist Downstream Processing and Purification This is an outstanding technical leadership position where you will be charged with leading a team of 2-4 people responsible for process improvement and downstream recovery activities. Your team will be responsible for running downstream purification studies, process validation activities, and process characterization activities of biologic products to support both on-site and 3rd party Contract Manufacturing activities. Your overall responsibilities will include executing PQ's on process equipment including Chromatography Skids, Bioreactors and TFF Skids. You will also be responsible for leading technical troubleshooting by designing scale down studies and analyzing statistical data from bulk manufacturing lots. Desired Skills and Experiences: ~ BS, MS or Ph.D. in Chemical Engineering, Biochemical Engineering, Protein Chemistry, Biology, Chemistry or related scientific field with 5+ years of biopharmaceutical industry experience. ~ Experience working with large-scale chromatography equipment for the downstream production of recombinant proteins and monoclonal antibody products. ~ Experience executing PQ's on process equipment including Chromatography Skids, Bioreactors and TFF Skids. ~ Experience executing Process Validation and Process Characterization activities. ~ Knowledge of cGMPs and GMP compliance. Want to interview today? Click Here to Do a Quick 2-Minute Online Interview! Are you a fit for this position? Please Click Here to Apply! (your information will be kept strictly confidential!) Looking forward to receiving your resume through our website and going over the position with you. Clicking apply is the best way to apply, but you may also: Email your resume in Word to: Amber.Howard@CyberCoders.com **Please do NOT change the email subject line in any way. You must keep the JobID: CC MonsterAp : JS-DPPIVS -- in the email subject line for your application to be considered.*** Amber Howard - Recruiting Manager - CyberCoders Apply Now! logET();PauseFooter(false);
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