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Performs independent technical review of documentation including Batch Production Records during and post-execution of cGMP activities. Oversees execution of remediation/CAPA activities required to continue production or move a process along.
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05 - 07 years of quality assurance experience in the pharmaceutical industry providing oversight to Manufacturing Operations, QC, and other cGMP areas. Provides guidance directives regarding remediation activities required to continue production.
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Five (5) to seven (7) years of quality assurance experience in the pharmaceutical industry providing oversight to Manufacturing Operations, QC, and other cGMP areas. Title: QA associate. Five (5) to seven (7) years of quality assurance experience in the pharmaceutical industry providing oversight to Manufacturing Operations, QC, and other cGMP areas.
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Provides guidance to MFG, E&T, and/or QC to ensure compliance with all applicable regulations and assists in resolution of issues identified. Works closely with others to recognize opportunities for improvement and drive change through the use of BIFI' Quality Systems.
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This includes providing plan creation oversight, verifying that changes adhere to local SOPs and regulatory compliance and ensuring communication/escalation of potential issues of broader impact to the business.
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Job Title: QA Associate III. Works closely with others to recognize opportunities for improvement and drive change through the use of client's Quality Systems. Responsible for providing quality oversight to the change management system for complex Minor and/or Major classified Change Controls.
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5 to 7 years of quality assurance experience in the pharmaceutical industry providing oversight to Manufacturing Operations, QC, and other cGMP areas. Job Title: QA Associate III Location: Athens, GA Type: Contract, Potential for extension or conversion to permanent Responsibilities Responsible for executing QA operations and overseeing junior team members as they assess, evaluate, and review operations on the floor (as defined above) against cGMPs to assure real time observation of activities, issue identification/ resolution including proper and timely documentation.
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5-7 years of quality assurance experience in the pharmaceutical industry providing oversight to Manufacturing Operations, QC, and other cGMP areas. 5-7 years of quality assurance experience in the pharmaceutical industry providing oversight to Manufacturing Operations, QC, and other cGMP areas.
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System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
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The Associate Scientist will provide daily care and health monitoring of animals; follow standard operating procedures and good documentation practices; organize, clean, and maintain production rooms, supplies, and equipment for egg layers.
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This position assures that all specifications are met prior to each stage of release to comply with USDA, FDA and cGMP regulatory requirements relating to these areas. Excellence in comprehension/application of USDA and EU regulatory requirements for production and distribution of regulated biological articles.
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One or more years of experience working in a Laboratory Animal Facility or performing work in cGMP environment. The PPU Technician will support the production facility by working shifts, weekends, and holidays as needed.
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Our client, a leading pharmaceutical company has a requirement for QA Associate in Athens, GA. Excellent employment opportunity for a QA Associate I in the Athens, GA area. Job Title: QA Associate. Company: A leading pharmaceutical company.
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Maintain compliance with SOP, current Good Manufacturing Procedures (cGMP) and regulatory guidelines. Accountable for area operations to accommodate production levels and donor arrival patterns.
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