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Cell/Gene Therapy experience preferred. Cell/Gene Therapy experience preferred. Lead a team of Batch Record Reviewers performing the following activities: Execute the initiation and/or evaluate deviation(s), interview personnel, analyze root cause, assess impact, identify corrective / preventive actions, present to management and close investigations in the Quality Management System (QMS.
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Knowledge of GMP requirements, Lean/Six Sigma, Validation. The Director, Manufacturing Integrator is a critical member of the Diagnostic Solutions (DS), Integrated Supply Chain (ISC) extended leadership team and the DS Operations team.
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Expertise in Cell & Gene Therapy. Our client is seeking a skilled Batch Record Reviewer Team Leader for our Cell & Gene Manufacturing facility in Maryland, USA. As the leader, you'll oversee batch record reviews to ensure accuracy and compliance with regulations.
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Further, all procedures and practices used are grounded in standards, regulations and laws addressing occupational safety (OSHA) and food safety and food quality (FDA) in addition to environmental safety (EPA) in accordance with Safe Quality Food (SQF) and Good Manufacturing Practices (GMP.
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Managing new multi-disciplinary project converting core-and-shell building into new EMA GMP rated cell and gene therapy facility. Managing new multi-disciplinary project converting core-and-shell building into new EMA GMP rated biopharmaceutical facility.
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The majority of our projects would be considered Construction Manager type with a GMP or Design Build. Our services now encompass general construction, furnishing and installation of architectural millwork, commissioning, joint ventures, diversity partnerships, construction management, historic wood restoration, plastic laminate, doors, frames, hardware, laboratory casework and miscellaneous specialties.
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Can streamline research by delivering operational and cost efficiencies through the strategic insourcing of GMP, GLP and non-GLP research services from discovery through safety assessment. We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development.
$17.2 an hourExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Follow all Coty safety and GMP guidelines. Follow all Coty safety and GMP guidelines. Painting and plastering. With Staff Management | SMX, you'll get a weekly paycheck, learn new skills, meet new people, and work with a great management team in a clean and safe environment.
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Execute the initiation and/or evaluate deviation(s), interview personnel, analyze root cause, assess impact, identify corrective / preventive actions, present to management and close investigations in the Quality Management System (QMS.
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At least 3 years of Quality Assurance experience in a GMP-regulated industry, such as pharmaceutical, biologics, or medical devices, or in combination with relevant education (Bachelor's degree or higher degree preferred, or equivalent experience in the pharmaceutical industry.
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To assist in quality-related activities that may include the preparation and review of GMP documentation. The QA Associate ensures compliance with cGMP and internal policies, procedures, and specifications.
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They will need to have at least 1-2 years’ experience in a laboratory setting, familiar with GMP and able to follow all procedures in the making of panels for the assembly side of the business.
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Demonstrates the ability to follow established procedures according to Good Manufacturing Practices (GMP) Responsible for validating processes and equipment that are directly related to filtration, cleaning and sterilization.
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Follow all safety guidelines and Good Manufacturing Practices (GMP) within the food and spices production and packaging area. TBest Services, Inc. is seeking Food Packaging Line Workers to join our client's expanding team in Hunt Valley, MD.
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Evaluate operating process equipment and implantation to ensure constant compliance with standard manufacturing practices (SMP). May develop weekly production plans coordinating resources (raw materials) and communicating relative priority to downstream parties.
$17.5 - $21.5 an hourExpandApply NowActive JobUpdated 1 month ago
gene gmp jobs in Towson, MD
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