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The Quality Manager (textile/leather manufacturing) will lead Quality Assurance efforts by identifying key quality factors, coordinating teams to implement preventative measures, and ensuring product consistency through process validation and corrective actions.
$140,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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You will make sure that product and process documents match the specifications based on established sampling and statistical process control procedures. Innova Solutions is immediately hiring for a Quality Assurance Associate.
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Functional support groups include Quality Assurance, Quality Control, Validation, Tech Transfer, and Quality Engineering. Learns to identify process issues. Functional support groups include Quality Assurance, Quality Control, Validation, Tech Transfer, and Quality Engineering.
$20.69 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Process Development Technician. 1-wk Tuesday/Wednesday/Saturday/Sunday - 2-wk: Monday/Thursday/Friday 2-pm - 2am. The incumbent will be required to solve problems regarding site assessment, specific units used in Biopharmaceutical manufacturing.
$21 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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1-wk Tuesday/Wednesday/Saturday/Sunday - 2-wk: Monday/Thursday/Friday. Manufacturing experience in a Good Manufacturing Practices (cGMP) or another regulated environment. Requires the moving of heavy equipment and the ability to lift :50 pounds.
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Tasks may be embedded in Standard Operating Procedures, operational and technical work practices and guidelines. Basic understanding of Good Manufacturing Practices (GMP). Significant reliance on supervisor.
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Job Title: Process Development Technician. Learns to identify process issues Innovation and Risk-Taking. Job Title: Process Development Technician. The incumbent needs to take the necessary safety precautions when working with pressurized systems, steam, and corrosive chemicals.
$21.42 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Audits & Certifications: Oversee external audits, regulatory certifications, and document control. Experience with Class II/III medical devices and manufacturing process tools (FMEA, Risk Management, Process Validation.
$130,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The individual in this role will work collaboratively with the analytical development team, quality control, and quality assurance to transfer and validate next generation analytical procedures for the testing of viral vectors, cell banks and gene therapy products in support of Genezen's services and commercial products in compliance with company policies and procedures and regulatory guidelines.
TemporaryExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Toolkits, SEIMs, Logrhythm, ACAS/Nessus/SCAP, mandatory/role-based access control concepts (e.g. SE Linux extensions to RHEL, PitBull, AppArmor, and Sentris) , video teleconferencing/VOIP, Oracle/MS SQL database security, and Apache/IIS Web server security.
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Minimum of 7-10 years quality assurance / supplier quality engineering experience in a pharmaceutical/life-science environment. Review and approve supplier deviations, change control, CAPA, and OOS investigations.
Full-timeExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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This role also integrates supplier selection, negotiation and contracting, and supplier relationship management with consolidation of spend in partnership across TechOps including but not limited to TechOps Supply Strategy & Planning, Quality Assurance, Quality Control, RNA Drug Substance, Gene Therapy Process Development, and Global Supply Chain.
$195,000 a yearFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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You will ensure that product and process documents match the specifications based on established sampling and statistical process control procedures. Mental agility to handle a large quantity and broad scope of different types of quality assurance work.
Full-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Provide support for Quality Assurance Reviews (QAR) and Corrective and Preventive Action (CAPA) plans, ensuring compliance and effectiveness. Facilitate and initiate change control processes, including PTCs and EM-PTCs.
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Product Testing: Area focuses on techniques such as SDS-PAGE Silver, QPCR, Potency, Kinetics assay, Enzyme Activity, pH, Osmo, A280 etc., in order to support in-process, release and stability testing.
$58 an hourExpandApply NowActive JobUpdated 27 days ago
control process assurance jobs in Wilmington, MA
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