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For your reference, we have included the original job posting below.
Chemist - Quality Control - Req. Code : 960.1
Job Number:
38391467
Company Name:
AMRI Global
Job Location:
Burlington, MA US
Job Category:
Science & Biotech
Chemist - Quality Control - Req. Code : 960.1
Chemist - Quality Control - Req. Code : 960.1
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Open Date 10/24/2011
Job Title Chemist - Quality Control
Education Bachelor's Degree
Location Burlington, MA Burlington, MA 01803, US
Career Level Experienced (Non-Manager)
Category Quality Control
Date Needed By 11/7/2011
Job Type Full Time
Travel Required 0 - 10%
Job Description
The QC Chemist is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished formulations, and for special projects; and for method development and transfer. Performance of analytical testing for incoming, in-process and final products, and stability samples. 2. Performance of raw material monograph testing. 3. Performance of QC analytical chemistry assays, HPLC, GC, IR. 4. Performance of wet chemistry assays. 5. Back up for QC analytical instrument maintenance, calibration, and validation. 6. Performance of QC general laboratory equipment maintenance. 7. Performance of QC method qualifications and validations. 8. Performance of QC method development. 9. Performance of cleaning validation studies. 10. Backup for review QC data. 11. Backup for QC analytical sample receipt for internal testing, login, processing, tracking, distribution of test results, and closure. 12. Backup for QC analytical sample receipt for outside laboratory testing, login, processing, shipment, tracking, distribution of test results, and closure.
# of Openings 2
Job Requirements Must be skilled in the use of computers and proficient is the use of word processors, and spreadsheets. Must have strong organizational skills and ability to prioritize and multi-task. Bachelor's degree in a scientific discipline. Minimum of 3 years working HPLC and industry experience in a GMP or GLP environment. Knowledgeable in FDA GMPs (21 CFR, 211, 820, and/or 600); ISO 9001 and 13485 a plus.
