• Insmed Incorporated (NJ)
    …documentation of reviewer comments, approvals, and version control in the company's document management system (eg, Veeva).Manage periodic reviews of approved ... ensure efficient coordination of MRC activities, compliance with company policies and regulatory standards, and the quality and integrity of all reviewed materials.… more
    HireLifeScience (12/06/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    regulatory requirements, policies and guidelinesExperience with Quality Control document reviews and regulatory inspection processesWorking knowledge of ... NJ. Role OverviewThe QC Specialist, Lab Services is responsible for sample management . The QC Specialist is encouraged to work independently on routine tasks… more
    HireLifeScience (10/17/25)
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  • Insmed Incorporated (San Diego, CA)
    regulatory inspections.Experience with Veeva QualityDocs /QMS and understanding of document management principles.Solid working knowledge of CSV guidelines ... and support to ensure Insmed computerized systems are deployed following lifecycle management and remain in a validated state per associated SOPs, regulatory more
    HireLifeScience (11/01/25)
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  • Cipla (Fall River, MA)
    …in the English language (Speaking/Reading/Writing) to understand work instructions and document results. Knowledge of fundamental cGMP and regulatory ... compliance to cGMP and set standards to meet the regulatory requirement and to ensure audit readiness. Ensure proper...in stores of a pharmaceutical organisation knowledge of material management module in SAP and cGMP in stores Proficiency… more
    HireLifeScience (12/02/25)
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  • USAA (Plano, TX)
    …initiatives including but not limited to: oversight of procedures/process, accurate regulatory reporting and filing, document governance, risk control ... Advisor Lead, you will be responsible for overseeing and guiding risk management and control activities across multiple critical domains. This individual will act… more
    job goal (12/14/25)
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  • Insmed Incorporated (NJ)
    …the opportunity to partner with business stakeholders to lead gathering, document , and prioritize requirements for campaigns, journeys, and audience targeting. ... data governance, and compliance policies (including privacy, consent, and regulatory requirements).Provide technical ownership of the Salesforce Marketing Cloud… more
    HireLifeScience (12/06/25)
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  • AUROBINDO (Durham, NC)
    …portfolio very quickly. The Aurolife family consists of an experienced management team with expertise in manufacturing, R&D, Quality Assurance and Quality ... control and regulatory affairs. In addition to several formulations under manufacture,...training forms in a timely manner and forward to document control for archival.Perform other duties as assigned. Qualifications… more
    HireLifeScience (12/06/25)
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  • Twist BioScience (South San Francisco, CA)
    …and present complex data in a clear and concise manner.Rigorously document experimental procedures, results, and conclusions, ensuring data integrity and ... Nanopore etc.), including corresponding sample preparation techniques, preparation and management of outputs from sequencing runs, and day-to-day operation and… more
    HireLifeScience (11/22/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    document control, process improvement, process validation and data management .Partners with Operational Excellence to implement improvements.Writes, reviews, owns ... permanent inspection readiness and actively supports internal audits and regulatory inspections.Provides input to studies related to process improvement and… more
    HireLifeScience (11/20/25)
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  • Cipla (Fall River, MA)
    …in the English language (Speaking/Reading/Writing) to understand work instructions and document results. Knowledge of fundamental cGMP and regulatory ... documentation and reports for accuracy Complies will all aspects of quality management system, cGMP policies, documentation and record keeping in accordance with… more
    HireLifeScience (10/22/25)
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