- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a Batch Record & Document Coordinator as part of the Technical Operations team based in Raritan, NJ. ... forms, etc. are printed and available for productionOversee batch records review and completeness of all associated documentation ensuring compliance with written… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Document Management Supervisor as part of the Technical Operations team based in ... Raritan, NJ. Role OverviewThe Document Management Supervisor will provide oversight of all GMP...all latest regulatory and quality requirements.Track relevant KPIsEnsure periodic review of all GMP documents are completed on time.Support… more
- AUROBINDO (Durham, NC)
- …and compliance with internal procedures.Reviews reports for accuracy and completenessMaintain the document review metrics to ensure that books are completed, ... operating procedures, and cGMPs. Previous GMP laboratory experience and technical reviewer experience are required. Review experience within an electronic… more
- buyer (Prairie Village, KS)
- …infection control protocolsAssist the dentist during exams and procedures as needed Document patient care and treatment plans accurately in the dental recordMonitor ... gender identity, national origin, disability, or veteran status. We regularly review our compensation practices and conduct pay equity audits to identify… more
- Merck & Co. (North Wales, PA)
- …the end-to-end regulatory submission process. The main focus will be on document production processes, including content authoring, review and finalization, and ... on requirements and design topicsSupport functional areas in identification and review of process questions and issues related to submission content management,… more
- Merck & Co. (Rahway, NJ)
- …Support critical reagent qualifications and SoftMax pro template validation activities. Document activities in a detailed and organized manner following ALCOA ... principals and SOPs. - Author and review technical documents. Complete assigned work within established project...assigned to support the evolving needs of the department. Document activities in a detailed and organized manner following… more
- Merck & Co. (Rahway, NJ)
- …and compliance in a regulated environment.- - Key responsibilities: - Enter, review , approve, and submit individual case safety reports for assigned products- ... Prepare and review aggregate adverse event reports and maintain aggregate report...other software such as SharePoint, learning management systems, and document management systems- Experience with pharmacovigilance databases and support… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …process, to ensure information is documented and reported timely.Folder Audit includes: Review HCP Engagements that are considered closed according to the policy ... head.Provide timeline to address issues and verify that issues were corrected and document the results in the audit check list.Provide, Manager, Manager of Meetings… more
- AUROBINDO (Dayton, OH)
- … Document work clearly and perform tests accurately.Prepare and/or review Test Procedures, SOPs, Validation Protocols/Reports as assigned.Perform maintenance and ... laboratory chemical waste, cGMP, cGLP, documentation) when performing tassigned activities. Review and prepare technical documents as required. Qualifications -… more
- Eisai, Inc (Exton, PA)
- …is essential.Prioritize, schedule, and monitor analytical projects, ensuring timely completion. Review and approve stability protocols relating to method development, ... assays and techniquesNegotiate service contracts with external providers. Assess and document CMO/CRO analytical proficiencies and readiness to perform various types… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …strategic and planning alignment across regions and functions and supports review of Local Country/Regional Medical Affairs activities when applicable. Provide ... evidence generating studies/projects. Manages all medical aspects such as study document development and drives execution for assigned projects in collaboration with… more
- Genscript USA Inc. (Piscataway, NJ)
- …lead for major capital projects, from design through commissioning. Review and validate design documents, technical specifications, and contractor submittals ... quality management, in collaboration with the Senior Construction Manager. Lead and document punch list resolution for MEP scope. Conduct periodic inspections and… more
- AUROBINDO (Durham, NC)
- …some guidance from Director. Organizes and presents data to support and document product development decisions. Leads investigations to support product and method ... exhibit stability studies and devises/supports corrective actions. Performs technical review of experiments and documents. Mentors junior analysts and… more
- Aequor (Golden Valley, MN)
- …of samples for Medallion Labs Deliver on time delivery for microbiological analyses Document results and review data Investigate any technical discrepancies on a ... timely basis Develop a strong knowledge of the analytical methods being used to analyze samples Maintain world-class lab safety environment that complies with all GMI and Medallion safety rules Minimum Qualifications: BS in microbiology, food science, biology,… more
- Merck & Co. (Lower Gwynedd, PA)
- …and associated lab automation-Accountability for generated data. -May review data generated by others-Understand and apply regulatory/compliance/scientific ... verbal and written communication -Ability to follow procedures and thoroughly document experiments -Ability to communicate results effectively in presentations to… more
- Aequor (Chattanooga, TN)
- …gained and lost distribution, risk and opportunities, and YOY media impact Review historical sales trends, research demand drivers, prepare forecast data and ... Associate may be asked from time to time to complete tasks not listed within the contents of this document , but that are relative to the goals of the business. more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …(ESRs) and may serve as deputy regional medical lead in Global IIS Review Committee meetings. May serve as medical lead for select company-sponsored evidence ... generating studies/projects. Manages all medical aspects such as study document development and drives execution for assigned projects in collaboration with USMA… more
- Merck & Co. (Rahway, NJ)
- …portfolio of work, holding the team accountable to deliver on priorities. Document preparation, maintenance, and review of documentation including specifications, ... testing protocols, testing reports, technical memos and supplier assessmentsRemain informed of current Good Manufacturing Practices, cGMP, and Good Distribution Practices, cGDP, and requirements and industry trends as described in worldwide regulations and… more
- Walt Disney Company (Bay Lake, FL)
- …encourage you to apply!"What You Will DoEvaluate new lawsuits, supervising document retention and coordinating case assignments.Support in revising written discovery ... coordinate company responses to consumer and government agency correspondence.May review and respond to consumer letters regarding intellectual property.Required… more
- vaco (Morristown, NJ)
- …business objectives.Familiarity with legal technology platforms such as eDiscovery tools, document review systems, or matter management systems.Proven ability to ... with compliance, HR, risk, and operations teams to proactively mitigate legal risks. Review and improve internal policies and processes to reduce exposure to… more