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BioLife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd. Monitors all systems and activities to ensure that source plasma manufacturing is performed consistently according to current Good Manufacturing Practices (cGMP), the Shire Quality System, and other applicable regulations for a plasma center.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Plasma Collection Center Quality Assurance Oversight: (80%) Reviews operational records to ensure they are complete, accurate and compliant with cGMP requirements. Employees must also maintain complete and accurate records, in accordance with cGMP.
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Consults and coordinates directly with the Center Manager on quality concerns within the plasma center. By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
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The function of a Senior Chemical Process Engineer is to ensure that process operations in the production and small scale facilities perform in a safe, predictable, and consistent manner, and are in keeping with safety, environmental, cGMP, and economic concerns in accordance with company and regulatory requirements.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Must have experience in a cGMP regulated environment and have worked in a medical device or pharmaceutical manufacturing facility. Minimum of 2 - 3 years previous experience in a medical device or pharmaceutical manufacturing preferably in a clean room environment.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Previous experience in FDA regulated biotechnology or pharmaceutical environment is strongly preferred. Maintain lab cleanliness and comply with cGMP compliance. Under supervision, the Production Lab Tech - Mfg Histology performs laboratory activities in the manufacturing lab including slide manufacturing events and packaging events and assists in tasks required for block qualification; follows the manufacturing schedule to complete required tasks per standard operating procedures involving basic laboratory techniques, calculations, material measurements, operation of laboratory equipment and record keeping as necessary.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Minimum of 5 years’ experience in validation, biological quality assurance and/or quality control in an FDregulated biotechnology or pharmaceutical company with progressive levels of responsibility.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The purpose of this position is to perform tasks and operations relevant to the bulk formulation and/or filling operations required for sterile production of liquid injectable pharmaceutical products under cGMP regulations in Drug Product Manufacturing.
$20 - $24 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Ensure timely manufacturing of all liquid parenteral cGMP products using aseptic processing technology to deliver high-quality sterile products to the pharmaceutical industry. High School Diploma or GED and a minimum of five (5) years of relevant related work in the pharmaceutical industry experience, plus one (1) year in a team leadership role.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations. Knowledge of basic laboratory and pharmaceutical production equipment including but not limited to: autoclaves, process tanks, incubators, analytical equipment, and CIP/SIP systems.
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Education: Minimum Bachelor's degree required with focus in the area of chemistry, biology or related science Licenses/ Certifications: Regulatory Affairs Certification (RAC Drugs) preferred Experience: At least 5 years’ pharmaceutical or biologics CMC submissions experience with FDA required.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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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. Our client, a leading pharmaceutical company has a requirement for QA Associate in Athens, GA.
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The right candidate must be familiar with pharmaceutical or related manufacturing processes and be thoroughly familiar with GMP/cGMP regulations (e.g. FDA cGMPs, ICH, IPEC, etc. SQA manages Supplier Audit and Supplier Development programs for customers in many industries including Pharmaceutical, Medical Device, Automotive, Aerospace, and Electronics manufacturing.
$1,000 - $1,300Full-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Specific expertise with Plumbing systems serving hotels, student housing, laboratories, power plants, Cogeneration facilities, manufacturing facilities, clean rooms, cGMP facilities and process systems for Pharmaceutical and microelectronics facilities is desired.
$86,000 a yearExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Able to perform operations and maintenance on utility systems, HVAC systems and/or manufacturing equipment in a CGMP Biotech/Pharmaceutical manufacturing environment. Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
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