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Prefer hands-on industry experience in cGMP/Biotech/Biopharmaceutical/FDA regulated industries. Proficient in Computer applications and software (Microsoft Excel, Outlook, Word, Access, Project); compliance specific software programs (Agile, Trackwise, LIMS, Master Control, ERP, etc.
$83,300 - $125,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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3 or more years of experience in cGMP/FDA/ISO and regulated OTC products. Review cGMP documents to ensure compliance. ALASTIN Skincare, Inc. is the fastest-growing physician-dispensed skincare company in the U.S. with innovative, scientifically proven and clinically tested products.
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Understand nomenclature for industrial parts and equipment as indicated on Piping and Instrument Drawings (P&IDs) Good understanding and ability to comply with industry standards and cGMP requirements.
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Current Good Manufacturing Practices (cGMP) regulations and Quality Management Systems (QMS). Start your next chapter and join MilliporeSigma. Deep understanding of the relevant process & analytical development, clinical and commercial manufacturing activities of APIs incl.
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At least five (5) years Quality Assurance related experience in a cGMP environment with a proven track record in batch documentation and quality control data review (with strong attention-to-detail), and lot disposition activities including handling / managing / resolving quality events and issues.
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Skellig is seeking an Automation Engineer with DeltaV and cGMP experience to support our clients across North America. Skellig is seeking an Automation Engineer with DeltaV and cGMP experience to support our clients across North America.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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5 or more years work experience in a cGMP regulated environment preferably in biologics manufacturing Prefer experience knowledge working with Single Use Technologies or modular operations. Benefits: Innova Solutions offers benefits( based on eligibility) that include the following: Medical & pharmacy coverage, Dental/vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident & Critical illness coverage, Pre-paid legal & ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP.
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The Maintenance Planner is responsible for planning and coordinating activities related to routine / non-routine maintenance activities, supporting and providing technical advice related to Preventative Maintenance/Repair activities of cGMP production equipment, utilities, and instrumentation associated with Manufacturing Operations under limited supervision.
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The Manufacturing Technician is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply.
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Establish and maintain the production unit in full cGMP and HSE (Health, Safety and Environmental) compliance. You will identify and implement programs and actions to ensure sustainable and reliable execution of manufacturing operations in alignment with cGMP regulatory expectations at the Carlsbad Site.
$144,000 - $216,000 a yearFull-timeExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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5 or more years of work experience in a cGMP-regulated environment, preferably in biologics manufacturing. May work in a clean room environment that requires gowning in the form of hospital scrubs, coveralls, gloves, and steel-toe boots be worn.
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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 6 days ago - UpvoteDownvoteShare Job
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POSITION SUMMARY: Manufactures in-vitro diagnostic products controls and calibrators used in the clinical laboratory following cGMP. Completes associated manufacturing documentation and participates in continuous improvement projects.
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Completes manufacturing batch records and MPIs, ensure compliance at all times in accordance with cGMP including GDP. Experience/understanding of Quality System Regulations and cGMP preferred.
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Develop and implement construction control plans, ensuring adherence to cGMP and regulatory requirements. We are hiring an experienced and driven Validation Engineer to support commissioning and validation projects, as well as overall design support.
Up to $80 - $120Full-timeExpandApply NowActive JobUpdated 11 days ago
cgmp job in Vista, CA
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