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Manage all aspects of a cGMP manufacturing campaign, including batch record review, safety evaluations, material procurement, equipment ordering/set up/cleaning and execution of the chemical operations.
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Our Science, Technology, and Industry (ST&I) Practice undertakes diverse projects in pharmaceuticals, biotech, cell and gene therapy, cGMP facilities, cleanrooms, and various other industrial sectors.
$80,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Plumbing, Piping, & Fire Protection Engineer will work to maintain project budgets, and may assist with cost estimations, and support marketing and proposal development. Job Description OverviewColliers Engineering & Design seeks a Plumbing, Piping, & Fire Protection Engineer to join our Science, Technology & Industry group.
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This role is responsible for overseeing routine virus and mycoplasma testing (cell-based and molecular biology assays) of manufactured commercial and clinical products according to cGMP, ICH guidelines, and associated standard operating procedures.
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Assist with all aspects of a cGMP manufacturing campaign, including batch record review, safety evaluations, material procurement, equipment ordering/set up/cleaning and execution of the chemical operations.
$57,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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The Associate DP MSAT Engineer also serves as a technical representative for CMO selection strategy, equipment qualification activities, and will be hands on solving issues during technology transfer and cGMP start up.
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Monitoring assistance to a cGMP operation. Large, rapidly growing biotech organization is seeking a temporary QC Analyst to join their team! Nesco Resource and affiliates (Lehigh G.I.T Inc, and Callos Resource, LLC) is an equal employment opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or veteran status, or any other legally protected characteristics with respect to employment opportunities.
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This position is responsible for coordinating sample management and method transfer activities to external laboratories for a wide variety of microbial and analytical techniques to support raw material, utilities, in-process, bulk drug substance and drug product manufacture in a cGMP regulatory environment.
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To be considered for the Quality Compliance Specialist position you must have a Bachelors in a scientific or engineering discipline or related field with the following minimum amounts of relevant experience for each level, in a combination of quality, production, engineering, regulatory (chemistry, manufacturing and control) and/or laboratory, with demonstrated accomplishments in effectively implementing cGMP requirements.
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CGMP experience and experience with technical writing is desirable. The primary purpose of this position is to perform analysis of manufacturing data from chromatography and other purification processes.
$19.5 - $22.5 an hourFull-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Summary: Support the Quality Control (QC) department by providing basic laboratory and. Duration: One-year contract with strong potential for extension or permanent hire. Calibrates or verifies calibration of instruments/devices prior to use.
$23 - $25 an hourExpandApply NowActive JobUpdated Today
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