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Experience Required for Your SuccessRequirements:BS in chemical or biochemical engineering, or related degree supplemented with relevant experience (MS in engineering preferred)Experience in pharmaceutical/biopharmaceutical industry or related industry/cGMP environmentDemonstrated experience with manufacturing processes and equipment such as CIP systems, filtration skids, chromatography and lyophilization equipment, etc.
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Our R&D Quality Control team seeks a talented Senior QC Analytical Chemist to join an innovative organization to serve as Cresilon's Subject Matter Expert (SME) and technical leader in cGMP Analytical Chemistry.
$110,000 - $135,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Knowledge of GCP and global cGMP regulations, (knowledge of EU GMP QP regulations is preferred), a plus. Knowledge of the operation and technical theory for the following analytical chemistry instruments: KF, FTIR, HPLC, GC, LC/MS, PSD, XRD, and DSC.
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At least 3 years, or more, of experience successfully selling analytical instruments or capital equipment and consumables to cGMP biotech, biopharma, and life science companies or related experience.
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Proficient experience with HPLC Method Development, Dissolution, Particle Size Analysis in cGMP setting. Utilize a range of analytical techniques and instrumentation, such as HPLC, GC, LC-MS, FTIR, NMR, and dissolution testing, to analyze and characterize raw materials and finished drug products.
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This position involves overseeing the production, storage, quality control, and distribution of induced pluripotent stem cell (iPSC) lines under cGMP conditions to researchers and scientists worldwide.
$180,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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As a QC Laboratory Analyst, you could work in an analytical or microbiological laboratory environment that stays in sync with Good Laboratory Practice (GLP) and current Good Manufacturing Practice (cGMP.
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We design, supply, and service a range of water systems and monitoring equipment in industries ranging from pharmaceutical to food and beverage applications, and from microelectronics ultrapure water to municipal water and industrial wastewater treatment.
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5 years or more analytical instruments capital equipment sales work experience preferred. Autonomous - Our teams work remotely, strategically managing their workload and schedule to ensure customer success.
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Extensive experience (+12 years) in quality assurance roles within the pharmaceutical industry, with a strong understanding of cGMP regulations, quality systems, and pharmaceutical manufacturing processes.
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The right candidate must be familiar with pharmaceutical or related manufacturing processes and be thoroughly familiar with GMP/cGMP regulations (e.g. FDA cGMPs, ICH, IPEC, etc. SQA manages Supplier Audit and Supplier Development programs for customers in many industries including Pharmaceutical, Medical Device, Automotive, Aerospace, and Electronics manufacturing.
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Must be Experienced in cGMP and GDP requirements for pharmaceutical manufacturing. Responsible for clinical manufacturing of cell therapy DS/DP within the Cell Culture Technology Center (CCTC.
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Handles and ensures quality of documentation (control, retention, and archival) to support CGMP activities. Accountabilities Handles CGMP documentation review related to product release, facilities and equipment, material controls, laboratory controls, packaging and labeling, and production & process controls.
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Bachelor's Degree in Biology, Biochemistry, Chemistry or similar Life Sciences discipline. This is a developed territory in the life science space with over two decades of growth, and our commercial group is looking to add a team member who will expand the business through customer focused activities, creative problem solving and continued professional development opportunities.
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Notes: Aseptic Cleaner High school diploma/ GED Pharmaceutical and clean room experience for the aseptic production of sterile products, cGMP experience. Notes: Aseptic Cleaner High school diploma/ GED Pharmaceutical and clean room experience for the aseptic production of sterile products, cGMP experience.
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cgmp job in Secaucus, NJ
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