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Conduct routine and non-routine microbiological testing of materials and cell therapy products (Gram stain, growth promotion, endotoxin, mycoplasma, sterility) Support Quality Systems such as; change control, deviation, CAPA, audits, quality metrics, etc.
$90,000 - $210,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Reject all products and materials that fail to meet quality expectations. Ensure that all packaging materials and processes comply with relevant industry regulations and standards, such as FDA regulations for food packaging or ASTM standards for materials.
$22 - $24 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Manage Supplier Change Requests and changes relating to supplier improvement initiatives Support supplier quality teams, to establish the processes for: Delivering quality parts, materials, and services, preventing defects.
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Sets up and performs destructive and nondestructive tests on materials, parts, or products. Performs movement of inspected materials through the ERP system. Records test data, applying statistical quality control procedures.
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Build, deploy and reinforce learning tools and materials to support quality event management capability development. Lead and facilitate Quality Event Investigations and subsequent CAPA development in accordance with defined timelines and in collaboration with appropriate subject matter experts.
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Performs customer order fulfilment to ensure shipments match the customers requirements, including: Sales Orders, Pick, Pack and Ship Processes, and Return Materials Authorization (RMA) An Associates or Bachelor's Degree in Mechanical Engineering, Electrical Engineering, Industrial Engineering, Applied Science, Applied Quality and Standards, Quality Systems Management, Supply Chain Management, or other related concentration is strongly preferred.
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Description: The Supervisor, Quality Assurance, schedules and coordinates daily priorities for incoming raw materials and labeling components, in-process testing, finished product sampling, in-process labeling and packaging operations, sampling and inspection activities on all work shifts.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Significant experience with quality systems, engineering design controls, sterilization, bio-safety testing of materials, controlled environments, clinical use of medical devices is also required.
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In support of the quality management system module leads maintain records of issues, enhancement requests and support the implementation of system changes. R&D Quality and Medical Governance.
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6+ years managing investigations Management (deviations, CAPA, etc) Experience managing RCA (Root Cause Analysis) Proficiency. Oversee the standard and timeliness of deviation and CAPA completion. 10+ years experience in Biopharma experience.
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Provide Quality Assurance technical expertise to ensure to ensure aseptic manufacturing facility, processes and support systems are in compliance with company guidelines and CGMP regulations marketed products and/or their raw materials, APIs, excipients or components.
$90,000 - $115,000 a yearFull-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Performs routine analytical tests of pharmaceutical raw materials, in-process samples, blends, finished products, and stability samples using instrumentation such as HPLC, UPLC, GC, UV/VIS, FTIR, dissolution apparatus, particle size analyze, etc.
Full-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Provides input to various layers of the organization including clinical affairs, professional marketing and consumer marketing on training and marketing materials to ensure that statements are supported by approved indications and relevant literature.
Part-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Scientist 3 - QC is responsible to perform testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculate and report results on applicable specification documents, participate in method transfer activities within departments or between facilities or organizations.
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Perform routine tests of raw materials, finished product and stability samples including dissolution, assays, chromatographic purity, content uniformity using UV and HPLC, particle size distribution using different techniques including Light Scattering (e.g. Malvern), density, water determination by KF, and tests according to the in-house monographs and USP in a regulated laboratory environment.
$38 - $40 an hourFull-timeExpandApply NowActive JobUpdated 3 months ago
materials job Title: quality in Piscataway, NJ
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