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The Associate for BioLegend’s Quality Control group will test products such as antibodies and proteins in the following application(s): flow cytometry, immunohistochemistry, western blotting, ELISA, multiplex immunoassays and/or functional bioassays.
$27.4 an hourFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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The Associate Director, Quality Control will lead all Quality Control aspects for GMP Operations in all phases of product development. Associate Director, Quality Control.
$190,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The OpportunityThe Associate Director, Quality Control will lead all Quality Control aspects for GMP Operations in all phases of product development. A strong technical background and proven track record in Quality Control related to biologics, oligonucleotide, small molecules, and AOC (Antibody Oligonucleotide Conjugate)/ADC (Antibody Drug Conjugate) modalities.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Oversee the development, implementation, and maintenance of robust quality, safety, and EHS systems, including Document Control, Training, Change Control, Deviation Management, CAPA (Corrective and Preventive Actions), and OSHA compliance.
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FULL DESCRIPTION : The Associate Director of Quality Assurance and Compliance is responsible for ensuring the highest standards of quality, compliance, and regulatory adherence across all aspects of our operations.
$160,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Maravai LifeSciences is seeking a #MiracleMaker to join our document control team as a Temporary Document Control Associate I. As a Temporary Document Control Associate I, you will play a critical part in ensuring the integrity and compliance of our document management processes within the Quality Management System (QMS.
$30 an hourTemporaryExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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This position is responsible for management of day-to-day tactical quality operations related to GLP, GCP and GMP (GXP) quality systems and supporting sub-functions (i.e., General Data Protection Regulations and Qualified Person (QP) requirements.
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Basic tissue culture and purification responsibilities include performing cell culture work, antibody purification, conjugation, and associated quality control steps including purity analysis, isotype testing, mycoplasma detection, and specificity measurement by assigned methods.
$53,000 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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The Quality Control Associate I, Lab Control is responsible for supporting the control and management of samples within QC and performing routine testing of in-process, release, and stability samples following written methods and procedures.
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The Associate Director will oversee outsourced analytical development and quality control activities supporting manufacturing, quality release, and stability studies of drug substances and drug products.
$230,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Skill and ability to maintain a variety of written and/or computer records for research activities including Standard Operating Procedures, quality control records, supply inventories, safety records, sequenced DNA library database, nucleic acid isolation and purification logs, etc.
$31.64 an hourFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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The primary responsibility of the Warehouse Technician is shipping/receiving of orders, quality control, inventory control and other warehouse related logistics. Perform basic quality control (QC) procedures, presentation of equipment and inventory control.
$20 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Mentors quality control associates. The QC Associate Senior must be capable of mentoring other quality professionals and working closely with other departments. This position requires hands-on laboratory work and close collaboration with the QC control team, Process Development Team, and the Operations team, and external clients.
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Must be able to demonstrate an working knowledge of import/export marketing and manufacturing relationships, including quality control/testing processes and programs and logistics. Normally requires a bachelor's degree or equivalent, preferably in , and a minimum of 2-3 years experience in global sourcing including experience in manufacturing processes, quality control and national chain or specialty chain retailers.
$97,200 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Knowledge and hands on experience with QMS data management software such as ACE, Track Wise, Master Control, ETQ, etc. Supports vendor management program, occasionally conducts on-site and paper audits, and establishes Quality Agreements.
$46.5 an hourFull-timeExpandApply NowActive JobUpdated 9 days ago
quality control jobs Title: associate in San Diego, CA
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