- Eisai, Inc (San Jose, CA)
- …approved promotional clinical trials, patient access to medication, and regulatory /compliance guidelines preferred.Experience with account planning and management ... profile, we want to hear from you. The Senior Oncology Sales Specialist is responsible for meeting/exceeding sales goals through promoting Oncology therapeutic… more
- Merck & Co. (Lower Gwynedd, PA)
- …Practices (GLPs), Information Communication Technology (ICT), Maintenance Management , Management Process, Mentorship, Pharmaceutical Regulatory ... Pharmacovigilance, Regulatory Affairs Compliance, Regulatory Affairs Management , Regulatory Communications, Regulatory Compliance, Regulatory… more
- Eisai, Inc (Milwaukee, WI)
- …approved promotional clinical trials, patient access to medication, and regulatory /compliance guidelines preferred.Experience with account planning and management ... your profile, we want to hear from you.The Senior Oncology Sales Specialist is responsible for meeting/exceeding sales goals through promoting Oncology therapeutic… more
- Merck & Co. (Omaha, NE)
- Job DescriptionReporting to our Company's Global Supply Chain Director, the Specialist will support the development and implementation of global trade compliance ... policies, procedures, and related training. The Specialist will interface with internal customers, external vendors, and service providers as needed. This role is a… more
- Merck & Co. (South San Francisco, CA)
- …enhance document authoring processes, thereby improving efficiency and compliance in regulatory submissions.The candidate will play a key role in developing, ... GenAI approaches to streamline the creation and quality control (QC) of regulatory submission documents. The candidate will be part of an interdisciplinary team… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …is responsible for maintaining and advising new projects on the Building Management System while collaborating with the Engineering team to provide necessary ... supervision and conduct testing Core roles include communication, compliance, risk management , and use of current technology System Design and Specification… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …skills.cGMP manufacturing.Metrology, Maintenance, facilities and utilities.Computerized maintenance management systems (CMMS).Scheduling and planning.EHS and ... Legend Biotech is seeking a Metrology Support Specialist as part of the Technical Operations team...instrument and mechanical system scheduling, planning, and work order management for cGMP Commercial Cell Therapy Manufacturing. This individual… more
- Merck & Co. (Rahway, NJ)
- …combination products globally.- Experience in design controls, device risk management , medical device, complex combination product kits, prefilled syringes, ... sites, External Manufacturing, R&D, Quality, Operations, Product Development groups, Regulatory Affairs, Procurement, and suppliers. Key Functions Work Independently… more
- Merck & Co. (Millsboro, DE)
- Job DescriptionSr. Specialist , Biosafety The Sr. Specialist of Biosafety is accountable for providing and managing an efficient and effective Biosafety program ... of federal, state, and local biosafety regulations, and advise management accordingly.Review risk assessments for biological materials and laboratory operations… more
- Merck & Co. (Rahway, NJ)
- …clinical supplies.-Interacts with key partner organizations such as clinical development, regulatory , quality and other supply chain areas to address clinical supply ... well as preparation and presentation of the clinical supplies information at Investigator Meetings for assigned protocols. - Support...At least 5 year s of experience in project management - - At least 5 years of experience in… more
