- Insmed Incorporated (NJ)
- …in. Are you?About the Role:We're looking for a Quality Management System (QMS) Specialist on the Analytical Development team to help us expand what's possible for ... using the Veeva Quality Management System to ensure alignment with regulatory and internal quality standards.Work closely with Quality Assurance, Regulatory… more
- Cipla (Fall River, MA)
- …GMP batch production records as well as SOP's. In this role the Documentation Specialist adheres to the company's document and SOP's procedures while ensuring ... Job Title : Pkg. Documentation Specialist II FLSA Classification : Professional, Exempt Work...equipment and products in compliance with site SOPs and regulatory guidance. Provides data to support management evaluation of… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- … regulatory requirements, policies and guidelinesExperience with Quality Control document reviews and regulatory inspection processesWorking knowledge of ... of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QC Specialist , Lab Services, II/III as part of the Quality team based in Raritan,… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Validation Specialist III as part of the Quality team based in Raritan, NJ.Role OverviewThe ... QA Validation Specialist role is an exempt level position with responsibilities...of technical, qualification, and validation activities including data or document review and approval as needed. This role will… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking an Operations Specialist as part of the Technical Operations team based in Raritan, NJ.Role ... and expertise in support of GMP investigations, change controls, document control, process improvement, process validation and data management.Partners with… more
- Takeda Pharmaceutical (Social Circle, GA)
- …the manufacturing processes involved in plasma fractionation. As a Department Specialist , you will ensure all fractionation operations comply with corporate ... policies, regulatory requirements... requirements (GMP, FDA, EMEA), and safety practices. The specialist works closely with cross-functional teams to ensure efficient,… more
- Usaa (Plano, TX)
- …to key team members in the business to identify, assess, aggregate and document risks and compliance controls, including risks associated with new or modified ... policies and procedures. Maintains and expands knowledge of the competitive/ regulatory landscape and the company's key challenges. Coordinates and responds… more
- Reed Smith LLP (San Francisco, CA)
- …structure make us the go-to partner for complex disputes, transactions and regulatory matters. Our team of 3,000 people (including more than 1,600 lawyers) ... for ourselves and for our communities. Position Summary The Deskside Support Specialist provides general and second-level application and hardware support to end… more
- Reed Smith LLP (Pittsburgh, PA)
- …structure make us the go-to partner for complex disputes, transactions and regulatory matters. Our team of 3,000 people (including more than 1,600 lawyers) ... for ourselves and for our communities. Position Summary The Product Support Specialist , AI Solutions provides day-to-day operational support for the firm's growing… more
- Usaa (Charlotte, NC)
- …key team members in the business to identify, assess, aggregate and document operational and compliance risks and controls, including operational and compliance ... systems Awareness and ability to apply risk and compliance laws, regulations, and regulatory expectations. Ability to work with internal and external partners in a… more
