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Participate in project kick-off teams improving quality aspects of product introduction, and have a fundamental understanding of quality systems, SPC, and control plans. Support quality improvement efforts, Internal Auditing and Continuous Improvement initiatives.
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Coordinate with key committees and medical management structures including but not limited to Hospital Leadership, DPH Chief Nursing Officer, infection control, pharmacy, medical records, quality improvement, and other required hospital committees.
$88,182.79 - $135,742.36 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Main Duties and Responsibilities:Develop and direct the implementation of changes to Process Control, Quality Control and Quality Assurance procedures to improve product quality, reliability, yield and cost effectiveness.
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Onto Innovation is a leader in process control, combining global scale with an expanded portfolio of leading-edge technologies that include: 3D metrology spanning the chip from nanometer-scale transistors to micron-level die-interconnects; macro defect inspection of wafers and packages; metal interconnect composition; factory analytics; and lithography for advanced semiconductor packaging.
$150Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Location:Please note this is a hybrid role, requiring minimum 3 days in the office – Rye, NY or Chelmsford, MA or Clearwater, FLAbout this role:The Fraud Specialist will deliver a range of support services in the areas of fraud, risk mitigation, quality control, compliance and anti-money laundering.
$62,000 - $77,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We are seeking a dedicated and experienced Plant Quality Manager to oversee quality assurance and control processes at our aerospace manufacturing facility. This position requires access to information protected under U.S. export control laws, including the International Traffic in Arms Regulations and/or the Export Administration Regulations.
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The CNC Machinist II produces machined parts by setting up and operating a computer numerical control (CNC) machine; maintaining quality and safety standards; keeping records; maintaining equipment and supplies.
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Requirements: Master's degree in Regulatory Affairs, Engineering, Life Sciences, or closely related technical discipline (willing to accept foreign education equivalent) and five (5) years of experience as a Regulatory Affairs Specialist or experience executing the complete lifecycle of product registrations before national and international regulatory agencies, including documenting internal processes for quality control, and coordinating post-market surveillance and reporting activities.
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Roles and Responsibilities: Inspects components, housings, and finished assemblies of electromechanical products for conformance to established work instruction, industry standards, drawings, etc., using low / high power microscopes, test equipment, and hand-held inspection tools.
$28 - $32ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Preferably knowledge to handle SAP, EDMS, LMS, Master Control etc. The Sr. Associate Compliance provides scientific support in the root cause analysis and closure of OOS investigations, OOT investigations and product quality complaints; ensures compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP) and Quality Management System standards, compiles monthly Quality metrics for internal and corporate review, and analyzes trends to implement corrective and preventive actions to mitigate adverse trends.
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Knowledge of vendor/supplier management Program Working knowledge of Trackwise to handle electronic Quality Manage System (eQMS) data, EDMS for SOPs and LMS for trainings. Ensure compliance of establish Quality Management System (QMS) and in compliance with corporate requirements and all applicable FDA Part , Part /, Part , ISO and Canadian Medical Devices Regulations (CMDR SOR/-), EU Medical Device Regulation.
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A day as a Quality Control Technician I (Monday - Thursday, 05:00 am to 03:30 pm) in Cirtec Medical. Assist with qualification and validation processes under Quality Engineer (QE) oversight.
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Excellent time management and organizational skillsWritten and verbal communication skillsBe knowledgeable of and follow the safety procedures as outlined by Monogram FoodsBe knowledgeable of safe food handling practices, HACCP, and quality control procedures in your department.
$18Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experience with DeltaV Process Control System and SAP in a cGMP environment is desirable. Actively leads a bulk chemical manufacturing production line working with other shift supervisors to ensure consistency across all shiftsDevelops weekly production schedule by partnering with Production Planning, Supply Chain, Quality, and Product Management teams.
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Quality assurance, Compliance, GMP, Document control, Batch Record, Batch Record Review, product release, investigations, Root cause analysis, iso 13485, audit, quality compliance.
$20 - $28 an hourFull-timeExpandApply NowActive JobUpdated Today
quality control jobs in Tewksbury, MA
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