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AMRI: Quality Control Chemist

AMRI

This is a Contract position in Burlington, MA posted November 21, 2020.

AMRI provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries.The QC Chemist is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished formulations, stability samples and for special projects, method development/transfers and cleaning study qualifications.

Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything.

We pursue excellence because our work has the power to improve patients’ lives with the pharmaceuticals we develop and manufacture.Responsibilities Performance of analytical testing for incoming, in-process and final products, and stability samples Performance of raw material monograph testing, as needed Performance of QC analytical chemistry assays, HPLC, GC, IR, UV, etc.

Performance of wet chemistry assays Performance of weekly water sample analysis for support of manufacturing Performance of routine cleaning sample analysis for support of manufacturing Back up for QC analytical instrument maintenance, calibration, and validation Performance of QC general laboratory equipment maintenance Performance of QC method qualifications, transfers and validations Performance of QC method development Performance of cleaning validation studies Backup for review of QC data Assist QC Management, as needed, in the completion of OOS/departure investigations for QC Backup for QC analytical sample receipt for internal testing, outside laboratory testing, login, processing, shipment, tracking, distribution of test results, and closure Bachelor’s Degree in a scientific discipline required Minimum 2 years’ working experience in HPLC industry and experience in a GMP or GLP environment Proficient use of computer software, including Microsoft Office Suite (excel, word) Strong organizational skills with the ability to multi-task Knowledgeable in FDA GMPs (21 CFR, 211, 820, and/or 600); ISO 9001 and 13485 a plus All interested applicants must applyOnline.

AMRI is an Equal Opportunity Employer.

All qualified applicantsWill receive consideration for employment without regard to race, color,Religion, sex, sexual orientation, gender identity, national origin, orProtected veteran status and will not be discriminated against on the basis ofDisability.