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CGMP environment work experience in clinical manufacturing of biologics or products intended for human use is preferred. Perform all GMP related activities strictly according to SOPs with accurate and complete documentation associated with the testing, in compliance with cGMP, principles of Data Integrity and good documentation practices.
$74,859.2 - $112,195.2 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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CGMP clean room experience required. Responsible for preparing for and execution of manufacturing batch records, work instructions and/or SOPs. Maintain up to date training records and documentation of all activities to meet cGMP requirements.
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Ensures compliance with all applicable Federal and State accrediting agency requirements in the testing of biopharmaceutical products manufactured in the current Good Manufacturing Practices (cGMP) facility.
$74,859.2 - $112,195.2 a yearExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Maintain compliance with SOP, current Good Manufacturing Procedures (cGMP) and regulatory guidelines. 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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Ability to write reports, correspondence, and procedure manuals according to CGMP (Current Good Manufacturing Practices) standards. Assists the Donor Services Manager with planning operational issues and development of the blood center’s objectives of collecting blood and/or apheresis blood components from volunteer donors.
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Knowledge of CGMP (Current Good Manufacturing Practices) regulations. Program and troubleshoot logic controllers and robotics systems (mainly FANUC) Strong proficiency in AutoCAD (electrical and inventor), and other design software.
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Our strong growth is creating great learning and career development opportunities throughout our company, and especially our donation centers. Part brand ambassador, part clinical technician. Employee assistance program (EAP.
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