Scientist (Regulated Bioanalytical)
Location: Andover Massachusetts
Description: A10 is presently looking of Scientist (Regulated Bioanalytical) right now, this job will be placed in Massachusetts. For detail informations about this job opportunity please read the description below. Location :
Andover, MA
Position Type : Contract
Experience Level :
Start Date / End Date : 11/11/2013 / 11/06/2016
! Description
Job Title: * Clinical-Scientific|Bench Scientist
JobTitle Description: Job Title: Scientist Project: Develop and validate ligand binding assays for regulated study support. In addition, the scientist will also conduct sample testing in support of regulated studies, maintain a GLP/GCLP compliant laboratory, and perform routine equipment maintenance and calibration
The position may require work in non-traditional hours during the regular work week (The non-traditional hours would likely be rare and a midday start; finishing mid-evening)
Phases to meet Deliverable:
Phase I (Complete 6 months from start) attain proficiency in routine sample testing, equipment calibration and maintenance.
Phase II (Complete 18 months from start) attain proficiency in ligand binding assay method development, able to independently plan and execute experiments needed to move project forward
Phase III ( Complete 3 ! year from start) able to function as a BA principal investigat! or or lead scientist on a regulated study.
Requirements;
Bachelor's degree required.
Candidates should have 2 to 4 years experience with LBA (ELISA, ECLA, LC-MS for large molecules routine sample analysis.
Prior experience with regulated (GLP and/or GCLP) studies is desirable.
The candidate will need routine sample analysis using immunoassay techniques.
Additional responsibilities include:
Oversight of instrument installation and organization of a new laboratory space.
The scientist should require minimal training and will support methods run on the instruments and participate in the maintenance of the instruments.
CANDIDATES MUST HAVE:
ELISA experience and/or regulated experience (GLP, GCP, or GMP)
1 year of direct Pharma experience also desired .
*** Notes: LC-MS experience not necessarily needed, looking for "GLP" position experience.
NO OVERTIM! E OR TRAVEL REQUIRED. ***
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If you were eligible to this job, please email us your resume, with salary requirements and a resume to A10.
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This job starts available on: Sun, 27 Oct 2013 00:14:30 GMT
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