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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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This resource will also provide QA support for program check and challenge of artifacts and documentation prior to submission to IA and milestone closure, development of process flows, management of the remediation program administrative duties, including progress reporting, the SharePoint site, creation of MCA, and other BAU program governance activities.
$68 - $80 an hourExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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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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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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Assist or lead preparation of deviation reports and the completion of resulting corrective and preventative actions (20%) Assist or lead program improvement including identification of recurring deviations and/or gaps in the quality program and initiation or revision of SOPs related to the data review and QC processes followed for Animal Rule/GLP studies (15%) Participate in QA, sponsor, and/or regulatory agency (e.g. FDA) audits (5.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Summary Description: As a Quality Assurance (QA) Specialist, you will assist the QA Manager in providing and improving quality efforts. The QA specialist is part of a QA Team that strives to ensure the company is consistently delivering high quality, coordinated documents to clients which incorporate their project specific criteria.
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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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The best fit candidate is one with a telecom and/or construction and QA/QC background who can inspect/evaluate work performed by field crews and processes to ensure compliance with established specifications and standards.
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Associate QA Validation Specialist : 0 – 2 years. Sr. QA Validation Specialist : 5+ years. QA Validation Specialist: 2+ years. The QA Validation Department at Regeneron is adding to their team.
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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 30 days ago - UpvoteDownvoteShare Job
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ProLogistix in Hebron is hiring for a 3rd shift Inventory Control Specialist in Florence. QA is the last line of defense before the material leaves the facility, so accuracy and attention to detail is absolutely vital.
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We are currently looking to fill a Sr. Quality Compliance Specialist (Material & Supplier Quality) position. 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.
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As an Email Quality Assurance (QA) Specialist for the client’s internal agency, you will be responsible for reviewing, proofing, testing, and making recommendations for improving the quality of email marketing efforts.
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Ability to learn and apply computerized systems for daily performance of tasks Ability to prioritize, manage multiple tasks, and meet deadlines Experience in the pharmaceutical/biotechnology industry (biotech preferred) To be considered for this position, you must hold a BS/BA in scientific subject area or related field and Associate QA Specialist: 2 years related experience QA Specialist: 4 years related experience Senior QA Specialist: 6 years relevant experience.
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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. This role is considered a QA function and may provide QA approvals where assigned.
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