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Knowledge on Computer Systems Validation, SDLC methodologies, 21CFR part 11, and cGMP including GAMP and EU Annex 11. Understanding of one or more of the following functions in the processing industry: Supply Chain Management and Optimization, Manufacturing Execution System, Real Time/Historian database, Advanced Process Control, Process Engineering, or Asset Performance Management.
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Maintain compliance with SOP, current Good Manufacturing Procedures (cGMP) and regulatory guidelines. With donation centers and team members throughout the U.S., Octapharma Plasma, Inc. collects plasma to create life-saving medicines for patients worldwide.
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Knowledge of environmental monitoring/ cGMP clean room behavior highly preferred. Participate in cGMP production of viral products as a part of the environmental monitoring process. Bachelor/ Associate in Life Sciences, or HS Diploma with 3-5 years of experience in a cGMP clinical production environment.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Familiarity with GMP/cGMP documentation and the project change cycle process. Proficiency in creating VMs or Disk Images, data collection, inventory control, hardware disposal, and data archival.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Perform high-risk sterile compounding in an ISO classified cGMP environment. Previous cGMP or LEAN manufacturing experience is advantageous. Your work will strictly adhere to USP / regulations, current Good Manufacturing Practices (cGMP), and departmental Standard Operating Procedures (SOPs.
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Works in accordance with QA Supervisor to provide quality assurance oversight where the business is responsible for adhering to current Good Manufacturing Practices (cGMP) including warehouse, manufacturing processes, inspection, labeling and packaging, batch record review, batch disposition and product distribution as applicable.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Our strong growth is creating great learning and career development opportunities throughout our company, and especially our donation centers. Part brand ambassador, part clinical technician. Employee assistance program (EAP.
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The Director, Manufacturing, is responsible for managing the manufacturing operations and associated logistics of the company’s cell therapy programs, including operation of the internal cGMP manufacturing on-site.
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Assists in qualification of cGMP facilities and analytical instrumentation in the Center for Molecular Imaging (CMI). Creates and implements SOPs for Good Laboratory Practices (GLP) and current Good Manufacturing Practices (cGMP) studies, conducts internal audits, and provides training to laboratory staff and trainees to qualify the facility.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Operate under a CGMP mandated facility and work within FDA guidelines. This position would report into the groups VP of Manufacturing and manage a team of managers. Operate under a CGMP mandated facility and work within FDA guidelines.
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Learns and maintains familiarity and compliance with all state and federal regulations, SOPs, Occupational Safety and Health Administration (OSHA) standards, Clinical Laboratory Improvement Amendments (CLIA), Current Good Manufacturing Practice (cGMP), and internal procedures.
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The university’s primary teaching hospitals are Memorial Hermann-Texas Medical Center, Children’s Memorial Hermann Hospital and Harris Health Lyndon B. Johnson Hospital. Certified Clinical Research Coordinator (CCRC) or Certified IRB Professional (CIP) preferred; and a comprehensive knowledge of GLP, IND/IDE, and IRB regulations.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Must have knowledge of basic principles, theories, laws, policies and procedures that pertain to compounding and cGMP. Compounding Pharmacy Technician. Must have knowledge of basic principles, theories, laws, policies and procedures that pertain to compounding and cGMP.
Full-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Responsible for participating in continuous training: cGMP training, technical skills, safety, performance improvement. Review change to cGMP documentation and re-train. The Floater is a critical role in the company which ensures the proper cleaning of the cleanroom, controlled environment and GMP laboratory environments.
Part-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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There are so many ways Octapharma Plasma can enhance your life and your career. Strong customer service skills and the ability to understand and follow protocol. We are growing at an impressive pace, and so is the positive impact of our work.
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cgmp job in Houston, TX
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