Quality Control Analyst I
Found in: Resume Library US A2 - 2 weeks ago
The Quality Control Analyst I (RP/ISO) is responsible for conducting routine analysis of materials including: Raw materials, in-process and finished formulations under general supervision and in accordance with standard operating procedures (SOPs). They compile data for documentation of test procedures and prepare reports. They also calibrate and maintain lab equipment. Occasional travel to our Tewksbury, MA facility may be required.
Responsibilities
Responsible for the performing of tests and/or calibrations and evaluations or results related to GMP, ISO and non-GMP materials and products as appropriate
Follow documented procedures and document test data as required
Utilize one or more of the following techniques to characterize organic and inorganic chemicals: FT-NMR, GC/MS, HPLC, FT-IR, and wet chemistry tests
Write test procedures as required
Any additional functions as assigned
Requirements
BS or MS degree in Chemistry, Chemistry Informatics or another relevant science concentration/degree, or relevant experience that will substitute for a formal degree
One or more years of industry laboratory experience with GC, GC/MS, NMR or HPLC experience required; QC experience preferred, GMP experience a plus
Hands-on experience with Biovia LIMS/LES system strongly preferred; Cheminformatics experience a plus
Must be able to multitask in a fast-paced environment and possess strong verbal and written communication skills
Must be able to work effectively independently and as part of a team
Benefits
CIL and CIS offer a competitive salary and comprehensive benefits including generous paid time off, Long Term Incentives, 6% matching 401K plan and health insurance with no in-network deductible.
CIL is an EEO/Affirmative Action employer.
Learn more about us on our website:
About Us:
Cambridge Isotope Laboratories, Inc. (CIL) is the world’s leading producer of and stable isotope-labeled compounds. With approximately 750 employees and laboratories in four countries, CIL specializes in the process of labeling biochemical and organic compounds with highly enriched, stable (nonradioactive) isotopes of carbon, hydrogen, nitrogen and oxygen. Our chemists substitute common atoms (e.g., 1H, 12C, 14N, 16O) with rare, highly valued isotopes (e.g., 2H or D, 13C, 15N, 18O) so that the final product can be readily measured or traced using mass spectrometry (MS) or nuclear magnetic resonance (NMR). CIL’s products are utilized in laboratories, medical, government and academic research centers and health care facilities worldwide.
We are proud that CIL products have contributed to medical advancements in cancer research, new-drug development, environmental analysis, and medical diagnostic research. In the past decade, as the fields of proteomics and metabolomics have developed as leading techniques for determining biomarkers for disease presence, progression and the monitoring of therapeutic response, CIL has worked closely with industry leaders and researchers to provide the stable isotope-labeled tools needed for improved quantitation and qualification of complex biological systems.
After decades of research, stable isotopes have found their place in an ever expanding commercial scale applications in pharmaceuticals, semiconductors, flat panel displays as well as other high technology fields specifically with deuterium oxide (D2O) and deuterium gases. Pharmaceutical companies have begun to investigate deuteration of molecules that may provide advantages over their existing nondeuterated counterparts. In addition, increasing research into the potential medical advantages of new deuterated drugs is also occurring. In high technology, deuterated organic molecules and deuterium gas are commonly used in the manufacturing of microelectronics and OLEDs, which contribute to the increased lifetime of the devices.
Learn more about us on our website:
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