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Experience with CMMS Systems (SAP, Maximo, Master Control, Blue Mountain, etc.) Truly unique to the industry, our on-demand cleanrooms as a service include cGMP-compliant cleanroom space, warehousing, and materials management.
Full-timeExpandApply NowActive JobUpdated 6+ months ago - 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.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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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. Review and approve supplemental logs, charts and other documents in support of cGMP Operations.
$20 - $28 an hourFull-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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At least 2 years of experience working as a QC data reviewer with knowledge of cGMP regulations. We are currently seeking an experienced Quality Control (QC) Data Reviewer to join our client's team in Andover, United States.
$55 an hourExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Knowledge to handle SAP, EDMS, LMS, Master Control etc. ability to lead QA medical device and combination products compliance and auditing operations, make sound decisions regarding evaluation of cGMP compliance, and leadership ability.
$160,000 a yearFull-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Experience and Skill Requirements: 10-15 years of cGMP QC testing experience within Bioanalytical/Bioassay/Virology with minimum of 8 – 10 years of personnel management. The Quality Control (QC) Bioassay and Virology Manager is responsible for oversight of the day-to-day operations of the QC Bioassay and Virology Testing group within the QC Operations (Ops) department in support of our clinical and commercial AAV-based products.
Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experience working with electronic document systems ( CMMS work orders ,LMS, Track Wise, Master Control ) or similar systems. Support pharmaceutical manufacturing plant, equipment, and utilities, and maintain compliance with all state and federal guidelines with emphasis on current Good Manufacturing Practices (cGMP) and Good Documentation Practices (cGDP) requirements.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Responsible for participating in continuous training: cGMP training, technical skills, safety, performance improvement. Normal responsibilities include detail document control (using Good Manufacturing Practices.
Part-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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System owner of the site’s validation and engineering program; drafts, defines, and revises submission packets, procedures to ensure compliance to cGMP, GLP, FDA and worldwide regulations. Thorough understanding of key supporting quality systems including change control, deviation / non-conformance, and CAPA. Expertise in root cause analysis.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Ensures compliance with GCP, GLP and cGMP guidelines both internally at Sarepta and at contract testing laboratories. The Director of QCTS is responsible for the supervision of QCTS personnel, and the optimization of department resource allocation according to project/program needs to assure activities occur in an efficient, timely and cGMP compliant manner.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Monitors Building Management System (BMS) and Critical Monitoring System (CMS), and documents / responds to alarms and event in accordance with cGMP guidance. Experience with control systems, PLC’s and BMS system operation.
Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experienced in ERP transactions regarding cGMP raw materials, inventory control and reporting. Innova Solutions is immediately hiring for a Material HandlerMaterial Handler M-F: 8-5, Overtime available Responsibilities: In this position, you will be responsible for performing and document daily warehouse operations in a cGMP environment.
$32 an hourTemporaryExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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45 Testing of raw materials per compendial and non-compendial methods for cGMP manufacturing use. 15 Project management – new instrument/equipment implementation, SOP creation/revision, validation protocol generation/execution, operational excellence/continuous improvement projects.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The Shipper Receiver I is responsible for activities related to the receiving of raw materials, control of inventory and shipment finished goods. The position works on assignments that are routine in nature where cGMP experience is required in order to perform work activities.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Establish overall analytical strategies, including analytical development plans, comparability strategies and analytical control strategies. Early-stage analytical testing (cGMP and non-GMP.
Full-timeExpandApply NowActive JobUpdated 7 days ago
cgmp control jobs in Reading, MA
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