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The Scientist reports to the Quality Control & Analytical Product Development, Manager/Senior Scientist/Principal Scientist. Maintain high quality laboratory documentation in accordance with applicable regulatory guidance and Site SOPs.
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Our Somerset location is the corporate headquarters for Catalent Pharma Solutions. Expertise in Instrumentation techniques: HPLC, GC, FTIR, UV, KF, and other wet chemistry testing." The Scientist will be performing routine analysis of Finish products using laboratory techniques and instrumentation such as HPLC, Dissolution, Karl Fisher, pH meter.
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Must understand and apply cGMP requirements applicable to quality control laboratory. Amneal is an Equal Opportunity Employer that does not discriminate on the basis of sex, age, race, color, creed, religion, national origin, sexual orientation, gender identity, genetic information, disability, veteran status, liability for service in the U.S. Armed Forces or any other characteristic protected by applicable federal, state, or local laws.
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Senior Quality Specialist will be the SME for the quality systems such as Document Management, Artwork review, USP Compendial methods and management of reference standard. 5 years quality experience, 3 years minimum in Pharmaceutical or medical device Quality Organization with handling of Annual Product Reviews (APRs), investigations, Change Controls, CAPA management and electronic quality system modules such as TrackWise, EDMS, SAP, etc.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Perform test and report data as per the Catalent approved procedures. Instrumentation techniques: HPLC,GC, UPLC, Dissolution, UV, KF. Work on lab instruments (HPLC/GC/UPLC, KF, Dissolution, Hardness, disintegration.
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Lead Study-specific staff members through the Veeva Quality Management System (QMS) process for Deviation and CAPA Management, if applicable. Assist QRM team members with the creation and maintenance of a regulatory framework for Quality Risk Management (QRM) related activities, including review or creation of Controlled Documents (e.g. SOPs, Work Instructions) and/or tools, and templates.
$46.7 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for an Analyst, Quality Control Analytics - This position will be located in Raritan, NJ.
$95,000 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Bachelor of Science in Analytical Chemistry/Pharmaceutics with equivalent industry experience. Master of Science in Analytical Chemistry/Pharmaceutics preferred. Perform Finish product Testing (Stability, development), QC release and data review.
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Perform Assay/Related Substances, Karl Fisher, Dissolution, Hardness, Disintegration etc. Perform Opex activities, data trending, SOPs revisions, as assigned. Analyst will perform Assay, Content Uniformity, Blend Uniformity, Moisture testing, related substances, dissolution on finish product.
$40 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Title: Sr. Quality Risk & Compliance Associate. Experience with Clinical Trial related systems, e.g. Clinical Trial Management System (CTMS), electronic Trial Master File (eTMF, preferably Veeva Vault), Electronic Data Capture (EDC, preferably Medidata RAVE) and Large Scale Data Analytics (such as SpotFire, CluePoints, JReview or similar.
$45 an hourExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Develop end-to-end product quality strategic plan for designated products with clear ownership for each deliverable with Process Development, Analytical Development, Manufacturing Science & Technology (MSAT), Quality Control, Supply Chain, Regulatory and CMC / Commercial Leaders.
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The Quality Assurance Document Control Specialist role is an exempt position responsible for supporting the document management process within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment.
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Ensure quality of design, execution, and publication of real-world evidence studies, and quality of models & tools developed for business partners. Learn more at this position, the Associate Director, Global Real World Evidence, will support strategy development and execution of industry-leading RWE capabilities and talent development across the Janssen Global Commercial Strategy Organization (GCSO.
$232,300 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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IT System Administration/Vault Owner in Veeva vault (Quality, RIM, Clinical), learning management system (ComplianceWire), validation lifecycle management system (ValGenesis), electronic signature systems (DocuSign.
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Course volunteers cheer for and encourage runners along the course route in assigned locations, direct runners to stay on the designated paths, provide traffic control where necessary, and hand out water to runners if at a designated water station.
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quality control jobs Title: service technician Company: Gpac in Hillsborough, NJ
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