Job Description Summary#LI-Onsite Location: Morris Plains, NJ, United States Relocation Support: This role is based in Morris Plains, NJ, United States. Novartis is unable to offer relocation support: please only apply if accessible. This is an
Engagement Manager We are seeking a highly experienced and client-focused Engagement Manager to lead strategic consulting engagements within the Life Sciences domain. This individual will serve as a trusted advisor to clients, driving large-scale transformation initiatives
Director, Gpv Compliance & Business Management The Compliance & Business Management (CBM) team supports key Pharmacovigilance (PV) operational, compliance, and business activities across the organization. This role ensures PV compliance, supports contract management, facilitates audit and
Senior Director, Small Molecule Drug Product Manufacturing BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly
Associate Director, Global Medical Review The Associate Director, Global Medical Review provides input into the medical review of safety data for investigational and marketed products. The role is responsible for ensuring high-quality medical review activities, consistency
Associate Director, GxP Compliance and Auditing Legend Biotech is seeking an Associate Director, GxP Compliance and Auditing as part of the Global Quality team based in Bridgewater, NJ. Role Overview The Associate Director, GxP Compliance and
Lead Auditor, Quality Compliance Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day,
Sandoz Biosimilar Regulatory Affairs Team Opportunity An exciting opportunity to join the Sandoz biosimilar team; and be part of bringing affordable medicines to patients and prescribers. The individual will support the US Biosimilar Regulatory Affairs team
Senior Manager, Sterility Assurance Working with Us Challenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every
QA Support Contractor The contractor will provide temporary QA support to maintain quality and compliance oversight of sterile pharmaceutical products manufactured by third-party partners. The focus will be on batch release, issue resolution, and regulatory compliance
Team Lead, TMF Operations The Team Lead, TMF Operations is responsible for maintaining Trial Master Files inspection readiness in compliance with the relevant Standard Operating Procedures, ALCOA principles, country regulations and industry best practice. The Team
Associate Director, CDMO Alliance Management, Global External Manufacturing (GEM) The Associate Director, CDMO Alliance Management, Global External Manufacturing (GEM) will serve as Otsukas representative and business partner toward our network of Contract Development and Manufacturing Organizations
Associate Director, CDMO Alliance Management, GEM The Associate Director, CDMO Alliance Management, GEM will serve as Otsukas representative and business partner toward our network of Contract Development and Manufacturing Organizations (CDMOs). This leader is responsible for