Scientist, Biologics Raw Materials
Eurofins BioPharma Product Testing North America
Date: 1 week ago
City: Columbia, MO
Contract type: Full time
Job Description
Job Summary: Eurofins BPT-Columbia is looking for a Scientist to join our Biologics Raw Materials team located in Columbia, Missouri. This individual will have one to three years of experience testing Raw Materials used in Cell and Gene Therapy applications. The successful candidate will perform method establishment and validations under cGMP guidelines on a diverse set of methods including, HPLC, GC, Amino Acid Analysis, Mass Spectroscopy and FTIR.
Responsibilities Include (but Are Not Limited To)
Designing, carrying out, and performing simple and complex experiments and procedures in accordance with all applicable regulatory (e.g. DEA, EPA, FDA, FIFRA, OECD, etc.) requirements as defined by protocol, method, and standard operating procedures (SOPs).
Perform method establishment and validations on a diverse set of methods including HPLC, GC, Amino Acid Analysis, Mass Spectroscopy, and FTIR.
Analyze data with software including Empower and effectively communicate results.
Utilize laboratory information management system (LIMS) with proficiency.
Is able to utilize equipment, facilities, and personnel to produce sound scientific results in a timely fashion for Eurofins clients.
Adheres to schedule according to Eurofins or contracting organization’s timetable and establishes daily or weekly routines necessary to ensure on-time delivery.
Job Summary: Eurofins BPT-Columbia is looking for a Scientist to join our Biologics Raw Materials team located in Columbia, Missouri. This individual will have one to three years of experience testing Raw Materials used in Cell and Gene Therapy applications. The successful candidate will perform method establishment and validations under cGMP guidelines on a diverse set of methods including, HPLC, GC, Amino Acid Analysis, Mass Spectroscopy and FTIR.
Responsibilities Include (but Are Not Limited To)
Designing, carrying out, and performing simple and complex experiments and procedures in accordance with all applicable regulatory (e.g. DEA, EPA, FDA, FIFRA, OECD, etc.) requirements as defined by protocol, method, and standard operating procedures (SOPs).
Perform method establishment and validations on a diverse set of methods including HPLC, GC, Amino Acid Analysis, Mass Spectroscopy, and FTIR.
Analyze data with software including Empower and effectively communicate results.
Utilize laboratory information management system (LIMS) with proficiency.
Is able to utilize equipment, facilities, and personnel to produce sound scientific results in a timely fashion for Eurofins clients.
Adheres to schedule according to Eurofins or contracting organization’s timetable and establishes daily or weekly routines necessary to ensure on-time delivery.
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