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The QC Microbiology Supervisor, CAR-T Manufacturing is an exempt level position with responsibilities for performing routine Environmental Monitoring sampling of the manufacturing facility utilized for cell therapy products for clinical trials and commercial operations in a controlled GMP environment.
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2+ years of experience in cGMP or cGxP at an operational level supporting manufacturing in a pharmaceutical or biotech environment, is preferred. This role will be hands-on resource reporting to the Quality Control Manager, Microbiology.
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Enter data in CELabs LIMS System Key Requirements and Technology Experience: Key Skills- MICROBIOLOGY, Lab, Environmental Monitoring. Microbiology lab experience strongly preferred Minimum 4 years of Environmental Monitoring experience Understand USP, EP, JP, and FDA microbiology testing requirements Intermediate level experience with Microsoft Word and Excel.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Understand USP, EP, JP, and FDA microbiology testing requirements. Ensure compliance with current Good Manufacturing Procedures (cGMP), USP, EU and other global regulatoryrequirements at all times.
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Ensure compliance with current Good Manufacturing Procedures (cGMP), USP, EU and other global regulatory. Microbiology lab experience strongly preferred. Bristol Myers Squibb is an equal opportunity employer.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Experience using LIMS required; CELabs LIMS Systems preferred. Enter data in CELabs LIMS System. Job Description: Quality Laboratory Technician. Participate in aseptic process qualifications, such as aseptic gowning and media reads.
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Our client, a leading pharmaceutical company, is hiring a Quality Laboratory Technician on a contract basis. TSR is a relationship-based, customer-focused IT and technical services staffing company. Communicate effectively with QC peers, cross-functional peers and management.
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Key Skills- MICROBIOLOGY, Lab, Environmental Monitoring. Immediate need for a talented Laboratory Technician. Key Skills- MICROBIOLOGY, Lab, Environmental Monitoring. Please review the job description below and contact me ASAP if you are interested.
$20 - $25.8 an hourExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Job Title : Laboratory Technician. System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan.
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The QC Microbiology Specialist, Lentivirus Vector (LVV) CAR-T Manufacturing is an exempt level position with responsibilities for performing routine Environmental Monitoring sampling of the LVV facility to support clinical trials and commercial operations in a controlled GMP environment.
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A thorough knowledge of cGMP regulations as referenced in The Code of Federal Regulations (21CFR) and their specific application to stability programs in a pharmaceutical manufacturing facility.
$40 - $65 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The Director, Quality Operations Head, Raritan Cell Therapy Manufacturing Operations leads and handles all aspects of Quality Operations in support of the Raritan CAR T manufacturing site, in full compliance with established cGMP, J&J and JSC requirements.
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B.S. Chemistry, Biology, Microbiology or relevant discipline. Strong understanding of stability ICH guidelines and cGMP regulation. Piper Companies is looking for a Principal Stability Scientist to be responsible for stability product strategy and oversight of product stability programs for commercial small molecules Drug Substances and Drug Products Oral and Sterile working for a Biotechnology company in New Brunswick, NJ.
$65 - $68 an hourFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Candidates must have experience gowning up, along with EM, bioburden testing, and water and air sampling to be considered for this roleSummary:+ Ensure compliance with current Good Manufacturing Procedures (cGMP), USP, EU, and other global regulatory requirements at all times.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Position Summary: The Director, Quality Operations Head, Raritan Cell Therapy Manufacturing Operations leads and handles all aspects of Quality Operations in support of the Raritan CAR T manufacturing site, in full compliance with established cGMP, J&J and JSC requirements.
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