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The GMP Lead Maintenance Technician: A motivated self-starter with prominent levels of initiative. Responsible for supporting and maintaining the GMP clinical/commercial manufacturing and facility process equipment, Pilot Plant and QC laboratory equipment.
$31 - $42 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Minimum of 5 years of automated equipment experience in pharmaceutical industry and strong experience working in GMP environment. May include Rockwell Automation, Honeywell EBI, Delta Controls Orcaview, and JCI Metasys Building Management Systems.
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Experience in quality control or GMP within a cell therapy or biopharmaceutical manufacturing environment is preferred, including raw material release. with 5+ years of experience in quality control testing, analytical development, or GMP; OR a Master's degree in relevant scientific disciplines with 3+ years of experience.
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Associates will be required to comply with all Food Manufacturing GMP policies and procedures. Job Types: Assembly, Equipment Operator, General Labor, General Production, Hand Packaging, Machine Operator, Machine Packaging, Manufacturing, Material Handler, Picker/Packer, Production, Shipping and Receiving, Warehouse, Maintenance.
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Basic knowledge of HACCP, BRC food safety and GMP principles. Strictly adhere to sanitation, GMP, and safety standards. Perform other duties as assigned support to Ferrara Candy Company business objectives.
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As a Sanitation Supervisor, you will report directly to the Sanitation Manager and be responsible for assisting in maintaining a clean and safe working environment for all employees, adhering to industry sanitation standards, and ensuring compliance with FDA, SQF, HACCP, FSMA, and GMP standards.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Adhere to all applicable good manufacturing practices (GMP), personal hygiene, and safe quality food (SQF) policies and procedures as described in the European imports - Sysco food safety training manual.
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A minimum of 6 years’ experience in a GMP quality assurance (QA) role. Understanding of one or more of the following processes preferred: GxP systems Serialization Infrastructure (IT and/or OT related) Manufacturing Execution Systems (MES) Process Control Systems (PCS) and Building Management Systems (BMS) PI Historian.
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Familiar knowledge of GLP and GMP requirements as they pertain to protein and gene therapy process development and Quality Control (QC) testing is a plus. Principal Scientist, Gene Therapy Analytical Development page is loaded Principal Scientist, Gene Therapy Analytical Development Apply remote type On-Site locations US CA San Diego time type Full time posted on Posted 3 Days Ago job requisition id R4430 Who We Are: At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values.
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Reporting to the Associate Director of GMP Quality Operations, the Manager/Senior Manager of GMP Quality Operations will provide day to day quality support to the various Arcellx GMP-relevant functions and will be responsible for the administration of quality standards, internal practices and continuous improvement as it relates to internal technical operations and collaborations with manufacturing vendors.
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Pharmaceutical facilities including GMP Aseptic and non-Aseptic Areas and Non GMP Areas. Assemble pipe sections, tubing or fittings using couplings, clamps, screws, bolts, cement, plastic solvent, caulking, soldering or brazing equipment.
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This position provides cross-functional GMP/GCP/GLP compliance support for ongoing and new clinical studies. Experience working effectively with CROs/CSPs. Expe rience with electronic Quality Management Systems and Trial Master File. Skills and Abilities A solid understanding of GCP, GLP, GMPs and CMC requirements is expected.
$155,000 - $190,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Method Development, hplc, method validation, wet chemistry, Gmp, Laboratory, R&d, USP Raw Materials Testing, USP Raw Materials Identification, analytical chemistry, research & development. This a GMP contract manufacturing organization with focus areas being nutraceuticals and cosmetics.
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Hire and provide oversight of Quality personnel with expertise in Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), Good Laboratory Practice (GLP), and Good Manufacturing Practice (GMP.
$200,000 - $250,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Helps develop departmental standard operating procedures and maintains GMP and non-GMP equipment history files to develop preventative and predictive maintenance programs and procedures to reduce mechanical downtime and to ensure that breakdown and repairs are minimized.
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