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DPS Group is seeking a qualified Senior Quality Assurance Operations professional to perform batch disposition, batch record review, deviation, CAPA and change control support at the Boston, MA client site.
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Awareness of quality principles and tools such as quality engineering, reliability engineering, Design of Experiments (DoE), management of change (MOC), document control systems, quality codes and standards.
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Prior experience with quality processes, including batch record review, material disposition, change control, product complaints, deviations, investigations, and CAPA management. Experience with quality management systems for handling of records such as change control, product complaints, deviations, investigations, and CAPA management.
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An established reputation in the local marketplace and recognized technical expertise in one of ERM's existing service offerings, which include, but are not limited to air quality and climate change, environmental, health, and safety compliance assurance, process safety, sustainability, and environmental permitting.
$158,400 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Monitor plants in common garden experiments; harvest common garden experiments; process lab samples (sort and count seeds, dry and weigh plant biomass); enter data; data quality control and assurance.
$13 - $15 an hourExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Lead and be responsible for project-specific CM teams including, GEI staff and sub-consultants, with functions including, but not limited to, Resident Engineering, Office Engineering, Construction Quality Assurance, Construction Inspection, Surveying, Materials Testing, Contact Administration, Change Management, Cost and Schedule Analysis, Document Control, Environmental Compliance Monitoring and Public Outreach.
$165,000 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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The Senior Sterility Assurance Engineer leads New Product and Change Control projects affecting product microbiology, sterilization, packaging, and biocompatibility. The incumbent reviews and approves laboratory records and reports, as well as prepares test protocols, change control assessments, and test reports.
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Experience within SQM role preferred, specifically in auditing and quality agreement negotiation highly desirable; experience within the biologic, pharmaceutical or medical device industry performing direct hands-on work in a Quality Assurance/Quality Control function with a strong familiarity with GMP Quality Systems and documentation; experience with global Audit guidelines.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Gmp, Quality assurance, batch record review, Capa, Audit, non conforming. Will be held responsible for: Reviewing and editing batch records Assisting in Document Change Control and reviewing history records for compliance.
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Advanced knowledge of environmental compliance-related areas for example: air dispersion modeling, stormwater, Spill Prevention, Control, and Countermeasure Plans, waste, water resources, Risk Management Planning, California Environmental Quality Act permitting, multi-media auditing, etc.
$126,604 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Ensures integration of Disposition process with other Quality Systems (Deviation/CAPA, Change Control, Validation) The Quality Assurance Sr. Engineer, DSM Disposition, is responsible for establishing and maintaining a robust and efficient disposition program at the Holly Springs, NC site.
ExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Support quality processes and systems across the product lifecycle including, but not limited to, change control, CAPA, deviations and investigations, label control, laboratory control, product quality complaints, Annual Product Quality Review (APQR), and management notification.
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This position indirectly supports ongoing manufacture of biological clinical trial materials by providing timely and compliant support for quality systems including Change Control administration, Calibration / Validation review, MasterControl system administration and workflow development, inspection management and hosting, internal auditing, supplier management, site Quality Council, quality metrics generation, and site-level compliance deliverables.
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Complete and install minor JCL (Job Control Language) changes via Serena Change Management package at the request of Divisional Information Systems Manager. Manage/maintain weekend batch job schedules for Foodservice and Grocery business units to ensure all schedules are complete, all weekly backups/maintenance jobs are successful, Quality Assurance install window is available, IPL window for both business units are available.
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POSITIONThis position will become part of the Design Quality Group which is located both in Germany and the US.In this role, the software design quality specialist will provide guidance and expertise on product development and change control to R&D, marketing, procurement and production.
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