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Minimum 3 – 5 years of Quality experience in the life sciences industry preferably with medical devices and or in bioprocess equipment and methods. Develop Quality plans for In-process and Final-Inspection of customized single use system of fluidic handling components for bioprocessing applications.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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The Scientist, Analytical Development & Quality Control is responsible for analytical development, feasibility, method qualification, routine, and stability testing of antibody drug conjugates and intermediates.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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A minimum of 3-5 years in Analytical Development and/or Quality Control preferably in a clinical stage biopharmaceutical company. Development, optimization, qualification, transfer, validation, and routine execution of analytical methods for proteins, mAbs, drug conjugates using techniques pertinent to LC (SEC, RP, IEX), LCMS, ELISA, CE-SDS, icIEF, and other wet chemistry techniques.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Minimum of 6 years of experience in drug safety/pharmacovigilance quality assurance or compliance within the pharmaceutical or biotech industry. Certification in pharmacovigilance (e.g., RQAP-GLP, PVQA) or quality management (e.g., ASQ Certified Quality Auditor) is a plus.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Manage projects including development and implementation of lake management plans, watershed planning, natural resource field investigations including aquatic plant surveys, water quality investigations, stormwater planning, benthic and fisheries surveys, sediment sampling and other watershed or limnological investigations for a wide range of potential clients.
$125,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Cross-Functional Collaboration: Consult with or, as our operations expand, plan to consult with other teams, including Non-Destructive Testing (NDT), manufacturing, and machining, to ensure that quality control measures are fully integrated into all aspects of production.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Typically requires a Bachelor's degree in Science, Technology, Engineering or Mathematics (STEM) Education and eight (8) years of Quality Experience (Assurance, or Compliance, or Engineering) or Engineering Experience.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Our client is seeking a Quality Control Bioassay Consultant to join their dynamic team. Author and support quality events including change controls, deviations, CAPAs, and OOS Investigations as required.
ExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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The Technical Writer will be expected to use their expertise to work independently to move quality records forward and ensure on-time closure. This position will work with Quality management to author and review documents in support of ElevateBio’s programs as well as routine QC operations.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Typically requires a Bachelor’s degree in Science, Technology, Engineering or Mathematics (STEM) Education and five (5) years of Quality Experience (Assurance, or Compliance, or Engineering) or Engineering Experience.
$163,000 a yearFull-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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The Quality Engineer is a member of the Systems Quality Team reporting to the Quality Manager - Systems. Drive CAPA associated with product quality through the organization to ensure that any findings or non-conformances are addressed quickly.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Contacts external to QC may include: Analytical Development, R&D, Quality Assurance and other Quality functions, Regulatory , Manufacturing, Facilities and Engineering. In addition, the individual may participate in more complex projects, operational excellence initiatives, and various quality systems with general supervision.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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We have an immediate need for an onsite Senior Software Systems Quality Engineer (Quality Assurance/Compliance) to support Land & Air Defense Systems (LADS). Familiarity with a Quality Management System (QMS) or Standard Operating Procedures (SOPs.
$163,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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This role will be reporting to the Electronics Category Supplier Quality Manager. We are looking for a Senior Supplier Quality Engineer with experience in the manufacturing, process control and monitoring of Electronic Assemblies of varying complexities.
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If you are interested or know of someone that would be a great match, please send a MS Word resume to John Marino at John@SourceRecruitmentSolutions.com Source Recruitment Solutions, LLC. Or apply now online by directly clicking the “ APPLY NOW ” link: #Quality #QualityAssurance #QualityAssuranceManager #QualityAssuranceJobs #food #HACCP #SQF #ConsumerProducts #Monster.com.
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Title: quality Company: Lfb Usa in Bedford, MA
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