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Follow 5S and Lean Manufacturing Principles and maintain cGMP compliance. We brew badass beers on both coasts at our breweries in Escondido, CA and Richmond, VA, and create amazing experiences at our Stone Brewing World Bistro & Gardens and Taproom locations.
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The Live Downstream Lab Technician I will work directly with live antigen, batching solutions and semi-finished products following aseptic technique and cGMP procedures. Document and maintain activity records according to cGMP regulations.
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Support Hoxworth Blood Center’s safety, cGMP and Quality Plan. May provide direct and/or indirect supervision to exempt and non-exempt staff (i.e., hiring/firing, performance evaluations, disciplinary action, approve time off, etc.
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3 + years of experience in Process Engineering related to biochemical engineering and/or protein biochemistry, scale-up principles and manufacturing of biologics (cGMP) Process development (PD) experience supporting cGMP manufacturing at large scale.
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CORE COMPETENCIES: PACKAGING TECHNICIAN I (0-24 Month Period) Must be proficient in two Packaging Zones (Zone 4 + 1 other) Review and begin building knowledge of required SOP and cGMP guidelines for position.
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Learn, understand and apply rigorous quality standards, Standard Operating Procedures (SOPs) and Current Good Manufacturing Practices (cGMP) Our manufacturing operations are around-the-clock to meet the needs of our customers.
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Maintain compliance with SOP, current Good Manufacturing Procedures (cGMP) and regulatory guidelines. Maintain compliance with SOP, current Good Manufacturing Procedures (cGMP) and regulatory guidelines.
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A minimum of 5 years of operations or quality Assurance experience within a cGMP environment in the biotech/biopharma industry and Cell/Gene Therapy cGMP manufacturing experience preferred.
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Our strong growth is creating great learning and career development opportunities throughout our company, and especially our donation centers. 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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Omeros is seeking a highly motivated individual to join the Quality Assurance team as a Sr QA Specialist to play a key role in supporting cGMP quality operations. Omeros' lead MASP-2 inhibitor narsoplimab targets the lectin pathway of complement and is the subject of a biologics license application pending before FDA for the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy.
$95,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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This position will report to our Quality Assurance Manager and focus heavily on reviewing documentation such as batch records, internal audits, and ensuring cGMP compliance. Review Quality Control documentation to ensure compliance with company procedures and cGMP and support issuance of CoAs and stability studies.
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Directs and coordinates analysis of products in compliance with cGMP regulations and SOPs. Strong knowledge of Cosmetic manufacturing processes, computer and equipment validation, GMPs, and product/process validation.
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Part brand ambassador, part clinical technician. Employee assistance program (EAP) Conduct basic screening procedures (e.g. reviewing health related documents, taking vital signs and performing finger sticks.
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Job description:Responsible for Vendor and Supplier ManagementResponsible for Supplier QualityResponsible for Auditing cGMP Our ClientOur client is an award-winning clinical development company.
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The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client Cell Therapy Above-site organization, including the document approvals, document change control process, periodic review and system reporting.
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