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To be considered for the Senior Manager role you must have a BS/BA in business or scientific subject area and 8 years of related experience in either cGMP manufacturing operations (clinical and/or commercial) or supplier management or equivalent combination of education and experience.
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We do a variety of project types spanning pharmaceutical, biotech, cell and gene therapy industries, cGMP facilities, cleanrooms plus other industrial facilities. We do a variety of project types spanning pharmaceutical, biotech, cell and gene therapy industries, cGMP facilities, cleanrooms plus other industrial facilities.
$124,000 - $182,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Good knowledge of CMC including analytical methodologies and technology transfer Must have strong communication, change management and managerial skills Strong knowledge and demonstrated implementation of Compliance Management - cGMP, technical operations, quality and regulatory systems.
$188,000 - $244,800 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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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.
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You have basic knowledge of regulatory compliance inclusive of cGMP, FDA regulations, familiarity with ICH guidelines, and EU regulations. Ensuring product integrity and company reputation by assisting in the monitoring of cGMP compliance at contract manufacturers and business partners.
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You will be a vital part of a team focused primarily on the implementation and support of Waters Empower Chromatography software in a highly regulated cGMP environment. Are familiar with regulatory and quality policies, procedures and documentation methods, ideally in cGMP biotech/pharma operations.
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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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Reviewing, editing, and revising documentation in accordance with cGMP standards. Work for a well-regarded biotechnology company in Rensselaer, NY as a QC Analyst - Analytical Sciences ! Reviewing, editing, and revising documentation in accordance with cGMP standards.
$23 - $25ExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Experience working in a cGMP pharmaceutical Quality Control Laboratory is preferred but not required. Ensures compliance with applicable cGMP regulations and SOPs. Maintain and update relevant SOPs for data review and reporting as needed.
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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 Today - UpvoteDownvoteShare Job
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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.
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Understanding of cGMP regulation and quality management systems for pharmaceutical operations. Thorough knowledge of cGMP/FDA regulations. Strong knowledge of cGMP/FDA regulations.
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Experience running and maintaining HPLCs/UPLCsKnowledge of cGMP is a plus. Preparing, running, and troubleshooting HPLC or UPLC instrumentation. Job DescriptionPreparation of protein samples, standards, and controls and well as both organic and salt mobile phases and cleaning solutions.
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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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Minimum 7 years in cGMP manufacturing operations or supplier management. Ensure compliance with cGMP and regulatory standards. Minimum 7 years in cGMP manufacturing operations or supplier management.
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cgmp job in Rensselaer, NY
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