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Ensures laboratory maintenance to sustain a safe, effective and productive environment and ensures that appropriate GLP/GMP procedures are followed. Knowledge of purification (chromatography, dead-end and depth filtration, tangential flow ultrafiltration/diafiltration, viral inactivation and viral filtration) preferred.
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The role of the Assistant/Associate Scientist is to conduct experiments for the purposes of providing robust and timely technical support for commercial downstream biopharmaceutical manufacturing processes consisting of purification (chromatography, dead-end and depth filtration, tangential flow ultrafiltration/diafiltration, viral inactivation, and viral filtration.
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Strong knowledge and background in GMP, GLP and GDP requirements Strong knowledgeable and versed in formulation development, process development; developing and documenting the data needed for drug related regulatory filings; and managing projects/products post commercialization.
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Maintaining GLP compliance for all laboratory work and documentation related to biospecimen data management and sample handling in accordance with FDA regulations and company SOPs. Assisting in maintaining GLP compliance in the laboratory.
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E.g. knowledge of FDA regulations, GMP/GLP/GCP, Lean Manufacturing, Six-Sigma, etc. e.g. knowledge of FDA regulations, GMP/GLP/GCP, Lean Manufacturing, Six-Sigma, etc. The Validation Engineer works alone and as part of the Engineering Department to author and execute IQ/OQ/PQ protocols, engineering studies, facility qualifications and other documents related to production and business systems.
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Maintain good laboratory practices (GLP). Knowledge of mechanical measurement equipment (e.g., Instron) and/or materials characterization capabilities (e.g., FTIR, DSC, TGA) is desirable. Assist in executing materials testing for sustaining engineering, new product development, or technology feasibility testing under supervision.
ExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Strong understanding of GMP, Good Laboratory Practices (GLP), FDA/ISO/BSI, Quality System Regulations (QSR) is required. A Bachelor’s degree in life sciences, or Certified Medical Technologist (MT)/Medical Laboratory Scientist (MLS.
$120,000 - $142,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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You will have the important role to generate high-quality immunoassay data in a regulated Good Laboratory Practices (GLP) setting to support Pfizer's vaccine programs according to Standard Operating Procedures.
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Thorough knowledge of applicable safety and standards guidelines, such as SOP, cGMP, GLP, DEA regulations and/or MSDS. Typical activities may include buffer/solution preparation, standard preparation and operating analytical instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc.
Full-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Ensuring that assays performed at external laboratories supporting Pfizer clinical studies are qualified or validated (as appropriate) and assay-associated tasks performed at external laboratories are done in a compliant fashion, in accordance with prevailing SOPs, and GCLP/GLP/GMP regulations, as appropriate.
$156,900 - $261,500 a yearFull-timeExpandUpdated 3 days ago - UpvoteDownvoteShare Job
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Strong knowledge and background in GMP, GLP and GDP requirements. Schedule:M-F Full Time. Builds and maintains strong working relationships with relevant internal and external partner groups (including Microbiology, Analytical Chemistry, Marketing, Manufacturing Operations, Regulatory, Clinical Affairs, and Quality, as well as external testing partners), ensuring that activities are managed collaboratively, efficiently, and effectively.
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Lead, Direct and Train lower level Chemists ( I, II) in the use of instruments, methodology, SOPs, WIs, GLP, GMPs, etc. Performance of diversified chemical testing as needed by using current USP,Standard Operating Procedures (SOPs), Work Instructions (WIs), Nice Pak's / PDI Test Methods (NPTM on raw materials, bulk liquids, and finished products.
$80,000 - $90,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Associate Scientist needed for a contract opportunity with Yoh Scientific’s client in. Hands-on lab work in a flexible, fast-paced entrepreneurial environment is essential. Assist in all areas of purification and all related duties.
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Quality Control : Ensure all laboratory work adheres to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP), following established Standard Operating Procedures (SOPs). Our client, a smaller to mid size pharmaceutical organization is looking for a Analytical Chemist III to join their growing organization.
$80,000 - $95,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Maintains good laboratory practices (GLP) consistent with MDS product development objectives and regulatory guidelines. Participate in Equipment and Test Method validations at the direction of the TMD/V&V group.
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glp job in Pearl River, NY
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