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Keywords: Microbiology, Microbiologist, QC, Endotoxin, Environmental Monitoring, cGMP, GMP, pharmaceutical manufacturer, manufacturing, Aseptic Manufacturing, Microbiological Laboratory Operations, regulatory, Utility Monitoring, environmental sampling, EM Plates, TOC analysis, Conductivity, Biological Indicators, KTA LAL, Bioburden, Growth Promotion, Micro-IDs, Gas Testing, LIMS, SAP, Trackwise, Investigations.
$30 - $35 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Proficiency in a Process Engineering role with a clear understanding of cGMP manufacturing and experience leading projects related to bioprocessing deviations, change control, process optimization, technical troubleshooting, and bioprocessing process changes.
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The Manufacturing Associate will be responsible for upstream unit operations (seed expansion, bioreactor operations, cell culture harvest), downstream unit operations (chromatography, tangential flow filtration, viral inactivation, and bulk filling) and/or manufacturing support operations (solution preparation, assembly preparation, parts wash, and autoclave) activities.
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About This RoleThe Manufacturing Sr Engineer I designs, specifies, installs, commissions and validates new process equipment, provides engineering technical support and troubleshooting for assigned process equipment and a GMP biological manufacturing area such as Cell Culture, Harvest or Purification.
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Perform and document cGMP manufacturing activities according to standard operating procedures, solution lot records and batch production records. Randstad Enterprises is looking for goal-oriented and professional Manufacturing associates to join our team.
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Ensures compliance/improvement of quality systems in manufacturing (i.e., ISO, QSR, GMP). Ensure compliance of quality systems in manufacturing (i.e., ISO, QSR, GMP) with applicable documentation updates (programs, drawings, work instructions, etc.
$86,000 - $117,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Located in Durham, NC, members of Life Edit work closely with the ElevateBio Research and Development and BaseCamp manufacturing teams in Waltham, MA. Life Edit is advancing therapeutic programs in collaboration with industry partners while building its own internal pipeline of gene editing therapies.
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You will perform complex compounding, manufacturing (cyclotron and chemistry module operation) and quality control processes (utilizing analytical equipment TLC, HPLC, GC), under supervision as required by State and Federal law.
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Arvato Digital Services LLC Country: United States of America State/Region: Kentucky City: Louisville Postal Code: 40229 Job ID: 189943 Date: Dec 13, 2021 Location: Louisville, KY, US, 40229 Nearest Major Market: Louisville Job Segment: Telecom, Telecommunications, Logistics, Warehouse, ERP, Technology, Operations, Manufacturing.
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Our market sectors include corporate headquarters, manufacturing, hospital/healthcare, pharmaceutical, defense, education, high-tech, sports and entertainment facilities and distribution. Business Services, Business Process Outsourcing, Property Management, Commercial Cleaning Services, Janitorial Services, Management Consulting Services, Business Support Services, Human Resources Consulting, Outsourcing/Offshoring, Energy Management.
$100,000 - $125,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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As a Contract Development & Manufacturing Organization (CDMO), our focus is to combine technical leadership in cell culture, microbial fermentation and viral vectors with world class GMP manufacturing facilities to advance tomorrows medicines.
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Must have working knowledge of regulatory expectations for the manufacture and testing of sterile pharmaceutical products with experience in quality assurance oversight of sterile manufacturing.
$30.5Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Your RoleWe are seeking a highly skilled and experienced CSV Engineerto join our team in Durham, NC. Develop and execute validation plans, protocols,and reports for computerized systems and commissioning and qualificationdocuments used in pharmaceutical manufacturing, ensuring compliance with FDAregulations (21 CFR Part 11), GxP, and other relevant guidelines.
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Examples of experiences include conventional & non-conventional machining, welding & joining, CNC programming, repair & overhaul, and lean manufacturing. Preference will be given to those with prior internship, co-op or military experience in manufacturing/supply chain or engineering.
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Are you a Controls Engineer looking to work on cutting edge projects in the manufacturing industry with a company offering streamline advancement to directorship? The company specializes in providing automation solutions to several different manufacturing companies so this will be a highly varied and challenging role.
$90,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday
manufacturing job Company: Google in Durham, NC
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