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Familiarity with GDP, GMP, Good Laboratory Practices (GLP), FDA, and ISO. Assembly, cleanroom, packaging, Production, Hand tool, Inventory, Inspection, Quality assurance, Packing, manual dexterity.
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Experience in GMP, ISO, and FDA controlled environments preferred. Need electronics technical background, experience with electronic assembly and test, preferably in medical device industry.
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Adherence to plant safety requirements, OSHA and QSR/GMP/ISO guidelines as applicable. Specific work experience required in use of Vision systems, electrical troubleshooting of circuits from low level signals up to 480 VAC, Allen-Bradley Programmable Logic Controllers (PLCs), and making modifications to Ladder Logic.
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Duties Safely and accurately process Customer products according to established procedures within FDA, ISO, and GMP guidelines. Skills STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention.
$13.02 - $17.08 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Knowledge of Good Manufacturing Practices (GMP), Quality System Regulation (QSR) and International Organization for Standardization (ISO) Assists Manufacturing Supervisor / Manager in overseeing production team to ensure all production operations comply with SOP's, cGMPs, QSR, GTP, and ISO standards as well as company procedures.
$28 - $30 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Exposure to cGMP's, established manufacturing practices and procedures, and compliance with GMP, QS, and ISO regulations and guidelines. This position will also support regulatory inspections (GMP and non-GMP regulatory compliance) including completing assigned corrective actions resulting from these inspections.
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Follow GMP, FDA, ISO, OSHA, and Gyrus ENT operational procedures. Performs direct labor production of vent tubes and implants on CNC lathe and/or mill according to process specification, prints and shop orders and/or MCI#s and prototypes.
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In depth knowledge of regulations and guidance supporting GCP and GLP to include FDA, EMA, ISO standards and ICH guidelines with direct impact to clinical programs. This position provides cross-functional GMP/GCP/GLP compliance support for ongoing and new clinical studies.
$155,000 - $190,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Follow all GMP,SQF and ISO standards. With $13 billion in revenue for fiscal year 2019 on a combined pro forma basis from operations, Berry is a leading global supplier of a broad range of innovative nonwoven, flexible, and rigid products used every day within consumer and industrial end markets.
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Routinely performs tasks in relation to cGMP, ISO, and Quality requirements including, but not limited to: Following basic and/or advanced Standard Operating Instructions, ensuring proper batch segregation, performing quality inspections, filling out paperwork accurately and timely.
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Adherence to FDA Regulations, GMP, ISO, HSE (OSHA), Department Procedures, and Manufacturing Directions. Ensures manufacturing line is operating at optimum level for a GMP environment in a Safe mode while meeting production goals.
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Knowledge of domestic and international regulatory requirements related to manufacturing, such as FDA GMP's and ISO standards preferred. Maintains general control to ensure compliance with domestic FDA/GMP and all international regulatory requirements.
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Lab Technician needs 1-3 years' experience with QC, GMP, and analytical procedures is required. Familiarity with the guidelines and regulations of FDA, OSHA, ISO and cGMP is preferred. Lab Technician needs 1-3 years' experience with QC, GMP, and analytical procedures is required.
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7+ years demonstrated ability in a GMP FDA, cGMP, ISO, or other regulated production environments. Ensure that the Visual Inspection Program operates to meet the requirements of approved production plans at minimum costs within established quality limits and in accordance with FDA, cGMP, ISO, and OSHA requirements.
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Knowledge of GMP (QSR) and/or ISO regulations. Receiving Inspector II, QC. Performs re-work, re-labeling, re-inspection of product returned from consignment and trunk-stock. Processes the receipt, re-work, re-labeling, re-inspection and inventory transfers of products returned from consignment and trunk-stock inventories.
$15.66 - $21.91 an hourExpandApply NowActive JobUpdated Yesterday
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