Performs various scientific analyses to evaluate the quality of raw materials, in-process materials, and finished goods and ensure compliance with established standards. Conducts and validates various biological and chemical quality control (QC) assays. Compiles, interprets, and documents statistical data from testing processes to either confirm compliance with established quality standards or identify deviations. May be responsible for establishing specifications for conducting assays and writing standard operating procedures. Typically requires a bachelor's degree. Typically reports to a sup ...ervisor or manager. Work is closely managed. Works on projects/matters of limited complexity in a support role. Typically requires 0-2 years of related experience.More Show Less
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Key Responsibilities. Chemical or Physical testing analysis of raw materials, finished products, stability or request samples. Documenting and submitting all raw data and results in LIMS. Preparation of reagents for chemical analysis including peer review. Knowledgeable in compendial (USP/EU) testing requirements and ensuring compliance per FDA 21 CFR.
Key Responsibilities. Chemical or Physical testing analysis of raw materials, finished products, stability or request samples. Documenting and submitting all raw data and results in LIMS. Preparation of reagents for chemical analysis including peer review. Knowledgeable in compendial (USP/EU) testing requirements and ensuring compliance per FDA 21 CFR.
Job Summary. The Quality Control Analyst is a key member of the Quality Control team. The QC Analyst performs analytical testing of raw materials, components, and intermediate/finished products. Job Responsibilities. Performs release and stability testing for raw materials, standards, components, and intermediate/finished products. Reviews laboratory data as assigned by Supervisor. Maintains proficiency with data acquisition systems. Calibrates a...
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that. the information I provide in my application will be processed in line with. Takeda’s. Privacy Notice. and. Terms of Use. I further attest that all information I submit in my employment application. is. true to the best of my knowledge. Job Description. Job Title. Quality Control Analyst I. Location. Brooklyn Park, MN. About the ...
POSITION SUMMARY. Under general supervision, the Quality Analyst I performs routine quality control inspection, testing and data analysis for various incoming, in-process, and final products within MSD’s protein-based immunoassay catalog. This position will execute various laboratory cleaning activities to help support overall operations of Quality/Product Control. DUTIES AND RESPONSIBILITIES. Complete testing of incoming, manufactured, and in-pr...
Quality Control Analyst I in Springfield, MO. Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The QC laboratory operates 24/7/365. This role may be assigned to the 2nd or 3rd shift depending on current staffing and training/qualifications. . The Quality Control Analyst is an integral part of the CURIA team, contributing to our success by testing raw materials, intermediates, ...
Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Analyst I based onsite in our Andover, MA facility. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureate...
Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Analyst I based onsite in our Andover, MA facility. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureate...
Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Analyst I based onsite in our Andover, MA facility. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureate...
Cambridge Isotope Laboratories, Inc. has an outstanding opportunity to join our GMP Quality Control team as a Quality Control Analyst I based onsite in our Tewksbury, MA headquarters. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor in...
Description. POSITION SUMMARY. Under general supervision, the Quality Analyst I performs routine quality control inspection, testing and data analysis for various incoming, in-process, and final products within MSD's protein-based immunoassay catalog. This position will execute various laboratory cleaning activities to help support overall operations of Quality/Product Control. DUTIES AND RESPONSIBILITIES. Complete testing of incoming, manufactur...
