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Quality, QA, assurance, GMP, manufacturing, distribution, packaging, CDMO, pharmaceutical, batch, release, systems, compliance, regulatory, specialist, investigations, CAPA, deviation, change, control, operations, senior, leader, supervisor, manager, coach, mentor.
ExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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The QA Specialist II supports the quality management system (QMS) through performing raw material release activities, acting as a system administrator for the document management system, and establishing & executing QMS procedures.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Partner with QA/QC Manager to create quality control processes, forms, and systems for tracking. Partner with QA/QC teams from General Contractor and Subcontractors to ensure Harris quality controls procedures are being adhered to.
$62,888 - $94,331 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Our client - a leading pharmaceutical and biotech CDMO - is seeking a QA Specialist join their growing team. Monitor, track, and review all quality system documents like Change control, investigation, validation, deviations, Complaints associated with batch release.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The QA Document Control Specialist is responsible for maintaining the document and record control systems to meet Quality Management System requirements and is responsible for coordinating the issuance, revision, review and approval of SOP’s and other documents.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Role: Senior Document Control Specialist (QA Specialist) Looking for Quality Assurance Specialist II who will effectively execute and maintain compliant Document Control Management System.
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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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Experience with MasterControl beneficial Responsibilities may be modified or added as needed and discussed with the Assistant Director of QA/QC and/or Associate Director of Quality and Facility Director.
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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.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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This position maintains site compliance of operations including, Manufacturing, Quality Systems, Quality Control, Quality Assurance, Facilities Maintenance, Materials Handling, and QA Validation in accordance with mandated regulatory requirements and site expectations.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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This role is responsible for overseeing quality and regulatory affairs, dealing with tasks like regulatory submissions, customer interactions, and change control assessments. Job Title: QA/RA Compliance Specialist.
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Serve as a backup Quality Control (QC) analyst for routine testing procedures in the CQC laboratory. Analytical Instrument Specialist Decatur, IL Ready for a Quality career with more impact.
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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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In accordance with the QMS and Quality Policy, the Sr. QA Specialist – Computerized Systems is responsible for supporting the implementation of a computerized system program. Support of computerized system applications through validation, maintenance, quality administration (such access control, system periodic review, etc.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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As a QA Specialist, a typical day might include the following: Interacts with Quality Control laboratories, support laboratories, and Facilities to ensure a successful compliance profile Provides consultation or advice in alignment with QA policies Active participation in investigation, evaluation, and problem resolution in support of Deviations, Change Controls, CAPAs, etc.
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