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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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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 11 days ago - UpvoteDownvoteShare Job
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Experience in a cGMP contract manufacturing organization is advantageous. Duties and Responsibilities: Perform various routine manufacturing tasks under the direction of internal SOP's and cGMP guidelines Prepare materials needed for manufacturing operations.
$22ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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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 10 days ago - UpvoteDownvoteShare Job
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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 25 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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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.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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5 or more years’ work experience in a cGMP regulated environment, preferably in biologics manufacturing. May work in the clean room environment that requires gowning in the form of hospital scrubs, coveralls, gloves and steel toe boots be worn.
$73 - $83 an hourExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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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.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Implementing improvements in areas such as cGMP training, core competencies, technical skills, safety, and performance management. Experience on demand planning, inventory management, sourcing, purchasing, and delivery performance.
$125,000 - $135,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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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.
ExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Strong knowledge of chemical engineering along with cGMP manufacturing focus. Managerial experience in cGMP manufacturing. Enforce cGMP guidelines. Peptide and oligo nucleotide manufacturing experience in upstream and downstream manufacturing (preferred.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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ESSENTIAL DUTIES & RESPONSIBILITIESFollow cGMP and ISO standards or guidelines as they apply to manufacturingAssemble cartridges and reagent kit componentsFollow manufacturing SOPsOrganize and maintain floor area and supplies used during work performedWork independently and as a part of an assembly line teamMaintain a safe work environment with respect to chemicals and equipmentResolve line issues and suggest improvementsOperate all manufacturing line equipment.
Full-timeExpandUpdated Yesterday - UpvoteDownvoteShare Job
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Lead all operational and technical CMC subjects (manufacturing, analytical development, validation, specification setting, stability, etc to deliver cGMP top quality drugs on time and on budget.
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Assist in maintaining an environment that complies with CFR, cGMP, and SOP's. Resolves employee relations issues and submit unsettled grievances to department Manager and Human Resources. Supervises, trains, and develops department staff to insure process control and efficient operations.
$70,000 - $80,000 a yearFull-timeExpandUpdated Yesterday
cgmp job in Carlsbad, CA
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