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This position will work directly with External Manufacturing Organizations (EMO) involving Pharmaceutical, Medical devices/Combination products, Consumer products /OTC and Biologics to ensure drug products/ Biologics are manufactured as per cGMP regulations and Bausch Health requirements.
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The position will be responsible for supervising the training team who lead training activities for the overall plant team members who support cGMP Clinical and Commercial Cell Therapy Manufacturing.
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This individual will oversee the Training team members in collaboration with department management in Operations and Quality to support personalized cell therapy production through safe and compliant operations according to cGMP requirements.
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The Operations Support Specialist will be part of the Technical Operations team responsible for the production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Intermediate knowledge of cGMP pertaining pharmaceutical facilities, utilities, and equipment. Knowledge of cGMP in the pharmaceutical industry. Intermediate knowledge of pharmaceutical manufacturing and utilities that support cell therapy clinical manufacturing.
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Janssen.com POSITION SUMMARY: This position is responsible for performing manufacturing procedures and the execution of scheduled tasks within a CGMP environment. We’re the Pharmaceutical Companies of Johnson & Johnson, and you can count on us to keep working tirelessly to make that future a reality for patients everywhere, by fighting sickness with science, improving access with ingenuity, and healing hopelessness with heart.
$49,088 - $66,413 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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General exposure and experience in a GMP/Validation discipline with a knowledge and understanding of pharmaceutical Design/Build/Commission/Validation processes and how they relate to regulatory requirements and cGMP regulations within the E.U. and U.S. FDA.
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The ideal candidate will have experience working within the lab as well as tech transfer within a cGMP environment and be comfortable going into a clean room environment to observe and gather data.
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Maintain the laboratories with good housekeeping practices and in compliant with cGMP. · Follow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment. Bachelor’s degree in Chemistry or related scientific field and 2+ years related experience in pharmaceutical analysis OR Master’s degree in Chemistry or related scientific field and 1+ year related experience in pharmaceutical analysis.
$38 - $40 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Our client, a leading pharmaceutical company, is hiring a Clinical Manufacturing Associate on a contract basis. Experience within cGMP/FDA regulated industry. Our client, a leading pharmaceutical company, is hiring a Clinical Manufacturing Associate on a contract basis.
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Less than one year in Pharmaceutical Packaging/Manufacturing. Packing Operator is responsible for safely operating the package equipment to package in-process products in accordance with Packaging batch record while following SOPs and Maintaining 100% cGMP & compliance during operations.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Required 3 - 6 years of pharmaceutical industry experience in operations, Quality or Tech. Services. Carry out all duties in accordance with Good Manufacturing practices (cGMP), Safety protocols and standard operations procedures.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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3-5 years’ in pharmaceutical manufacturing involving change control, quality assurance. Support Document Control, Training Program, stay informed on regulations, cGMP trends, FDA/ICH Guidelines.
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Minimum of 7 years relevant working experience in a pharmaceutical or biotechnology company of which preferably 3 years in validation or QC, and in QA/CSV. Thorough knowledge of cGMP, in manufacturing and R&D within GxP regulated industries.
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Minimum 3 years of experience in Pharma Industry (cGMP Environment) in the area of process equipment and facility trouble shooting. Maintain Documentation as per company’s and cGMP requirement.
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pharmaceutical cgmp jobs in Raritan, NJ
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