- Unknown (New York, NY)
- …risks, structural weaknesses, and process gaps. The VP will also be expected to document review findings in a clear and structured manner, collaborate with ... Vice President, Credit Risk Review About the Company Prominent banking institution Industry...Company is seeking a Vice President for Credit Risk Review . The successful candidate will be responsible for conducting… more
- Insmed Incorporated (NJ)
- …cross-functional teams (Regulatory Affairs, CMC, Clinical, Quality) to facilitate document authoring, review , approval, and publishing workflows.Conduct ... requirements. The role has a strong focus on eCTD publishing and document management within Veeva Submissions Vault, ensuring accuracy, compliance, and timely… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …also provide oversight of technical, qualification, and validation activities including data or document review and approval as needed. This role will be ... within the siteReview and approve qualification/validation documentation (specifications, protocols, reports). Review and approve periodic review documentation for… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Document Control Specialist as part of the Quality team based in Raritan, NJ.Role ... OverviewThe QA Document Control Specialist role is an exempt level position...with workflow handling and electronic system usage.Manage the periodic review process for procedures.Issuance of batch related documentation in… more
- Cipla (Fall River, MA)
- Job Title : QA Document Control Associate FLSA Classification : Full-Time, Professional Work Location : Fall River, MA Work Hours: General Shift: 08:30 AM - 5:00 PM ... QA QMS Lead Salary Range : $64,272 - $77,662 PURPOSE The QA Document Control Associate in a pharmaceutical environment is responsible for managing controlled… more
- Twist BioScience (South San Francisco, CA)
- …quantitated high-throughput and attention to detail.Required to proofread, prepare, create, review , edit, and update Quality and Technical Documents including, but ... Synthetic Biology Manufacturing, and Gene Manufacturing highly desirableExperience with document management systems required.Experience with Learning Management Systems.Experience with… more
- 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
- 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
- Unknown (Cary, NC)
- …construction projects, leases, and insurance. This role involves a significant amount of document review , as well as the preparation of reports, guidelines, and ... disputes and litigation, as well as a strong background in the preparation, review , and negotiation of design and construction contracts. The ideal candidate will… more
- Insmed Incorporated (NJ)
- …of science, we're in. Are you?About the Role:The Associate Director, Medical Review Committee (MRC) Operations is responsible for managing the operational execution ... of the company's Global We're looking for an Associate Director, Medical Review Committee Operations, on the Medical Review team to help us expand what's… more
