- VTI Life Sciences (San Diego, CA)
- …and ambitious engineers looking to accelerate their careers in the pharmaceutical , biotechnology, and medical device industries. We offer an opportunity to ... services related to equipment, instruments, and systems for clients in the biotech/ pharmaceutical / medical device industry. This field service role will be based… more
- Sanofi Group (Cambridge, MA)
- …from account management and customers by analysing all available quantitative data and qualitative insights. + Create and perform pre-and post-deal financial ... that align with company objectives and present them to the Pricing Committee for review and approval. + Manage the timely and accurate preparation, review ,… more
- West Pharmaceutical Services (Jersey Shore, PA)
- …other transfer Project Managers + Gathering and analyses of numerous required data (operation, manufacturing, quality) and information for TT Requirements plan. + ... resources on managing required PNR and deviation investigation + Compiling, review and approval of Technology Transfer Equivalence Protocol (document defining… more
- Chiesi (Cary, NC)
- …management of Tagetik, SAP, BW, and Board systems and related reporting + Review Tagetik master data and reporting hierarchies periodically, ensuring consistency ... self-care). We are proud to be the largest global pharmaceutical group to be awarded B Corp Certification, a...leaders and BU heads + Budgeting/Forecasting: + Creation and review of departmental budget templates + Assist department managers… more
- Sanofi Group (Morristown, NJ)
- …teams accelerate progress. This individual will be responsible for providing regulatory review and approval of US promotional and other product and disease-related ... Affairs (US RA AdPromo) as a member of cross-functional brand and portfolio team review committees (RC), providing regulatory input into the review and approval… more
- West Pharmaceutical Services (Williamsport, PA)
- …of quality are achieved and maintained. **Essential Duties and Responsibilities** + Review and approval of metrology reports, where appropriate, for batch release ... + Establish and maintain documentation in line with West Williamsport and West Pharmaceutical Services Quality Systems. + Liaise with customers and suppliers on new… more
- Endo International (Horsham, PA)
- …three facilities, including Production Planning, Warehouse Operations & Logistics, and Master Data Management. + Develop and Implement supply chain best practices. + ... assessed in a timely manner. + Ensure ERP Master Data is maintained and kept current. + Lead supplier...Regularly assess material inventory levels at all plants. + Review MRP with respective team members and order/adjust, orders… more
- Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
- …aspects of downstream process technology transfers to CDMOs, including documentation review , gap analysis, and risk assessment. + Provide expert technical oversight ... of downstream manufacturing operations at CDMOs, including review of batch records, deviation investigations, and change controls. + Lead or significantly contribute… more
- Otsuka America Pharmaceutical Inc. (Augusta, ME)
- …aspects of upstream process technology transfers to CDMOs, including documentation review , gap analysis, and risk assessment. + Provide expert technical oversight ... of upstream manufacturing operations at CDMOs, including review of batch records, deviation investigations, and change controls. + Lead or significantly contribute… more
- Cambrex High Point (High Point, NC)
- …analytical and spectroscopic techniques and be able to interpret the corresponding data and spectra. + Ability to conduct literature searches for specific target ... ability to manage projects on-time without supervision. + Ability to author and review comprehensive reports at the conclusion of projects for internal and customer… more