- Legend Biotech USA, Inc. (Raritan, NJ)
- …the team responsible for QA oversight of final CAR-T product batch record review and release practices.Lead the establishment and improvement of QA practices to ... ensure accurate documentation of all review and release activities, including manual and electronic practices.Establish and implement cGMP procedures to ensure… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …provide guidance and determine immediate path forward for manufacturing quality issues. Review of all documentation, in accordance with Good Documentation Practices ... (GDP). Review , revise, or draft Standard Operating Procedures (SOPs)Support processes...benefits, family planning and care resources, well-being initiatives, and peer -to- peer recognition programs - demonstrating our ongoing… 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 ... Operations and other cross-functional and regional stakeholders.- Provides support in review of investigator-initiated studies (IIS) and may serve as deputy compound… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …incorporate all latest regulatory and quality requirements.Track relevant KPIsEnsure periodic review of all GMP documents are completed on time.Support documentation ... commuter benefits, family planning and care resources, well-being initiatives, and peer -to- peer recognition programs - demonstrating our ongoing commitment to… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …oversight of technical, qualification, and validation activities including data or document review and approval as needed. This role will be responsible for ... within the siteReview and approve qualification/validation documentation (specifications, protocols, reports). Review and approve periodic review documentation for… more
- Geisinger (Wilkes-Barre, PA)
- …new skills focused on the specialized practice settingFree Princeton NCLEX Review Questions (on-line, self paced)!Temporary Practice Permit (TPP) reimbursement + ... roleProvided with education and resources through professional development meetings, peer support, dedicated preceptor, mentor, and moreJoin the Geisinger Family!… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of engineered autologous T cell therapy products.Write and/or review user requirements, functional requirement specifications, qualification protocols, enterprise ... expertise in automation projects from user requirements, design evaluation, specification review through to testing and implementation in a GMP manufacturing… more
- Merck & Co. (Cincinnati, OH)
- …data. -Virology RMSDs are responsible for facilitating and developing peer -level relationships with scientific leaders in the external medical/scientific community ... on areas of therapeutic interest and our Company's data or productsConduct peer -level scientific discussions and maintain a reliable presence to ensure SLs have… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …such as planning advisory boards, managing individual stakeholder interactions and peer to peer discussions, congress engagement activities, and collation ... (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… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …manufacturing processes.Provide support in project management, purchasing, shipping, and invoice review for technical teams.Ability to work autonomously as well as ... commuter benefits, family planning and care resources, well-being initiatives, and peer -to- peer recognition programs - demonstrating our ongoing commitment to… more
