- Merck & Co. (Omaha, NE)
- …Finance, IS Audit, Policy Development, Policy Implementation, Policy Procedures, Problem Solving, Project Risk Assessments, Regulatory Affairs Management ... Job DescriptionReporting to our Company's Global Supply Chain Director, the Specialist will support the development and implementation of global trade compliance… more
- Eisai, Inc (Dallas, TX)
- …cognitive impairment due to Alzheimer's disease (AD) or mild AD. The Neurology Account Specialist (NAS) will be part of a diverse team of sales professionals who ... marketplace.Seek out mentorship to learn and build key sales skills. Qualifications: Specialist - ADBachelor's degree with 3+ years experience in two or more of:… more
- Merck & Co. (North Wales, PA)
- Job DescriptionSenior Specialist on the Patient Access team leads all promotional and resource asset work for our Company's Patient Access COE for the US ... review process management, Pharmacovigilance and Compliance point for department. - Senior Specialist partners with our US Hub vendors and creative agencies to… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist III as part of the Quality Operations team based in Raritan, New Jersey. ... Role OverviewThe QA Shop Floor Specialist is an exempt level position responsible for the...will include but not limited to tasks mentioned above.Support regulatory inspections and audits as needed.Consistently perform tasks in… more
- Eisai, Inc (Cincinnati, OH)
- …profile, we want to hear from you. The Senior Oncology Sales Specialist is responsible for meeting/exceeding sales goals through promoting Oncology therapeutic ... assigned territory in a compliant and appropriate manner. The Senior Oncology Sales Specialist represents and promotes assigned brand(s) in the IV and oral markets… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …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, ... NJ. Role OverviewThe QC Specialist , Lab Services is responsible for sample management. The...and handle corrective and preventative action recordsSupports internal and regulatory auditsRequirementsA minimum of a Bachelor's degree or higherA… 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...is a plus.Strong knowledge of GxP compliance.Experience in cGMP regulatory body audits.Strong interpersonal and written/oral communication skills.Ability to… more
- Legend Biotech USA, Inc. (Omaha, NE)
- …in the treatment of multiple myeloma.Legend Biotech is seeking Cell Therapy Account Specialist as part of the Sales team based in Omaha, NE (remote). Role ... OverviewThe Cell Therapy Account Specialist is responsible for representing Legend's products and services...with Corporate, PhRMA, and OIG guidelinesStrict compliance with all regulatory agencies, state, and federal law is requiredAdheres to… 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 ... permanent inspection readiness and actively supports internal audits and regulatory inspections.Provides input to studies related to process improvement and… more
- West Pharmaceutical Services (Exton, PA)
- Sr. Specialist Regulatory Affairs, MD Requisition ID 71773 Date Nov 21, 2025 Location Exton, Pennsylvania, US Department Regulatory Affairs Description This ... and planet through our sustainability efforts. Job Summary The Regulatory Affairs Sr. Specialist is responsible for...Able to comply with the company's safety and quality policy at all times International regulatory competency… more
