- 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
- Merck & Co. (Rahway, NJ)
- …Documents, Foreign Filing, Intellectual Property Management, Lawyering, Legal Analysis, Legal Documents Preparation, Legal Document Writing, Legal ... the office. The successful candidate will be expected to: Review , draft and/or develop legal documents and...be expected to: Review , draft and/or develop legal documents and communications independently. Independently handle legal… more
- Merck & Co. (Millsboro, DE)
- …and implement appropriate forms of contract and commitment with suppliers. Liaise with corporate legal as needed for review of contract language. Must have a ... meetings, schedule routine reviews and be able to translate and document Stakeholder requirements into tangible business results.Relationship Management - Work with… more
- Tris Pharma (Monmouth Junction, NJ)
- …serves as primary operational liaison across Market Access, Trade, Finance, Legal , and Analytics functions, ensuring seamless execution of contracting, pricing ... other payer contracts, including redlining contract language, coordinating cross-functional review and approval workflows, and ensuring execution consistent with… more
- Cipla (Fall River, MA)
- …SOP's. In this role the Documentation Specialist adheres to the company's document and SOP's procedures while ensuring their accuracy, quality, and integrity. This ... to the following : Works with Manufacturing/Packaging to deliver timely batch record review across all shifts. Reviews and approval of master batch records. Develops… 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
- Cipla (Fall River, MA)
- …execution. In this role the Validation Engineer adheres to the company's document and SOP's procedures while ensuring their accuracy, quality, and integrity. This ... Creates training materials for subject matter input. Track and manage periodic review . Develop strategies and documents for cleaning and process validation of API… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …will also provide oversight of technical operations activities including data or document review , risk assessments, CAPAs, and continuous improvement activities. ... process, operational, and quality improvements for manufacturing.Assist in the review and development of process-related protocols and documentation.Provide technical… 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)
- …system (LIMS)Prepare documents and coordinate Sample shipment (internal and external shipments) Review logbooks and/ or LIMs to align physical quantities of samples ... of regulatory requirements, policies and guidelinesExperience with Quality Control document reviews and regulatory inspection processesWorking knowledge of Quality… more
