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The QA Specialist will have oversight of and involvement in, GMP compliance for production of Clinical Trial Material (CTM), including work performed by Contract Manufacturing Organizations (CMOs.
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Under the direction of the QA Document Control Supervisor, the QA Specialist – Document Control, will control the movement, filing, archiving, and securing of all documents with the objective of ensuring compliance to company policies and procedures.
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Updates records for Organic, Non-GMO Project, Kosher, Halal, and other product certifications during supplier quality new ingredient approval. Monitors manufacturing process changes, updating organic records to confirm compliance.
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This role may be a fit for you if you have: Rigourous attention to detail Strong communication and organizational skills To be considered for this role you must hold a BS/BA degree in related field and the following amount of relevant experience for each level: Specialist: 2 years experience in QA/Document Control/Records Management Sr. Specialist: 5 years experience in QA/Document Control/Records Management May consider another degree field with relevant experience.
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The Quality Records Specialist will process external deviation and change records from our Contract Test Laboratories (CTL). Quality Records Specialist. Provide communication, support, and guidance to CTLs within the QA vector and upstream material team.
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Assists the IT Specialist in installing and configuring computer software, installing computer hardware peripherals, including the setup of network printers, monitors and mobile devices and provides assistance to the QA groups in UAT testing as assigned.
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The Quality Assurance Specialist will assist the Compliance Manager & QA Safety & Facilities Manager with document organization, document control, and activities supporting Fullscriptâs cGMP practices.
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The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for BMS Jump site records management. Quality - QA Associate Specialist – Document Control.
ExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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The QA Specialist will support all business units through direct support of the eQMS License Holders. The QA Specialist will provide reports to Management, as requested. Quality Assurance Specialist (eQMS and Document Management.
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The QA Records Management Specialist is responsible for applying established policies and procedures to facilitate the management of physical records in a GxP environment. 3+ years of relevant experience in information governance, records management, data governance, knowledge management, or library work.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The Quality Systems Specialist will be responsible for updating and maintaining an accurate QA Master Index to reflect the current revisions and status of the documents controlled through Quality Assurance.
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Job Title - QA Associate I. Scans, verifies and archives documentation and records. Responsible for filing and maintenance of controlled documents and records. Job Title - QA Associate I.
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The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client Jump site, including the document change control process, issuance and reconciliation of batch records, batch related forms, product labels, and management of archival and retention of GMP records.
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General warehousing tasks, customer support, requisition, shipping, receiving, building medical kits, inventory management, QA and cargo preparation, and deployment, including medical controlled items stored in a secure location, operation of various materials handling equipment, and utilizing updating DoD MMIS records.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Electronic Records & Electronic Signatures (Part 11), cGMP Bachelors Degree with a concentration in IT/Computer Systems 4 to 5 years of experience in Pharmaceutical industry or computer systems management Good knowledge in cGMP environment.
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