- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking a Sr . Associate OpEx Engineer as part of the Technical Operations team based ... holistic continuous improvement and problem-solving program to improve safety, compliance , cost, process stability building quality and efficiency into processes… more
- Aequor (Thousand Oaks, CA)
- …the manufacturing floor. Detail Oriented, Team player and Quality Experience. The Sr . Associate Quality Assurance position supports 's Quality Assurance program ... issues, providing recommendations, and assuring progress of quality records to completion. The Sr . Associate will also represent functional area quality for the… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking an Associate Director for Operations Compliance and Investigations Managementas part of ... the Technical Operations team based in Raritan, NJ. Role Overview The Associate Director for Operations Compliance and Investigations Management will provide… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Management:Manage 3rd party vendor interactions to ensure they are following compliance with all DSI requirements and meeting all service level agreements.Analyzing ... and FMV process to comply with DSI Legal and Compliance requirements. Work closely with HCP Engagements to manage...to track HCP Speaker trainings and other activities as required. Compliance and Policy Adherence:Primary point of contact for the… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good Clinical ... against project goals and milestones to monitor and ensure compliance with Daiichi Sankyo Clinical Study Oversight Plan (CSOP).Responsibilities- Reconcile… more
- Eisai, Inc (Nutley, NJ)
- …labeling, sales training and media/digital materials. Works to ensure Eisai's compliance with pharmaceutical laws including the Anti-Kickback Statute, False Claims ... Act, PhRMA Code and FDA regulatory guidelines. Serves as the legal representative on promotional and scientific review committees. Manages the legal and reputational risks of assigned business clients. Helps drive the implementation of legal strategy and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders.Summary The Associate Director, RACMC Portfolio Products, will be responsible for regulatory CMC ... regulatory process optimizations on relevant topics.Responsibilities- Supports CMC regulatory compliance activities for portfolio biologics to meet US, International… more
- Merck & Co. (Durham, NC)
- …issues to improve manufacturing performance, and maintaining the automation systems in compliance with cGMPs. The Manufacturing Automation Sr . Specialist must ... Job DescriptionPosition Description: Senior Specialist, Manufacturing Automation The Senior ...reviews automation documents, preventive maintenance, and SOPs to ensure compliance with GMP and safety.Assisting in the development and… more
- Insmed Incorporated (Bridgewater, NJ)
- …to manage multiple clinical trials (all phases), and ensure compliance with SOPs, FDA regulations, GCP, ICH guidelines, etc.ResponsibilitiesAdditional representative ... responsibilities will include, but not necessarily be limited to, the following: Works with global cross‐functional team to ensure that trials are conducted in adherence to study protocols, applicable SOPs, FDA regulations, project plans, ICH/GCP guidelines,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …access, and trade analytics. Relationships This position will report to a Director/ Sr . Director of Semaglutide Insights & Analytics. Will also work closely with ... Associate Manager, Semaglutide Integrated Analytics. Extensive interaction with the...purchases Build business use cases to gain Privacy and Compliance department approval to appropriately analyze patient-level data compliantly… more
- Merck & Co. (Durham, NC)
- Job DescriptionPosition Description: Senior Technician, MaintenanceThe Senior Maintenance Technician is responsible for providing equipment troubleshooting and ... Quality, Automation, Technology, and other groups as required.The Lab Senior Maintenance Technician will provide maintenance supporting vaccine process equipment… more
- Merck & Co. (Durham, NC)
- …within the site is seeking a highly motivated individual for a Senior Calibration Technician position. This individual will partner with Maintenance management, and ... maintenance, and engineering support for the manufacturing in Durham, NC. The Senior Calibration Technician is recognized as a knowledgeable resource in maintenance,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …striving for simplicity, making quality a proactive consideration, ensuring compliance with relevant Good x (eg clinical, distribution, manufacturing) Practice ... Canada), and escalating quality concerns. Relationships This position reports to the Associate Director of GXP Oversight and/or Head of GXP Support. Multiple… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …other research areas centered around rare diseases and immune disorders. Summary The Associate Director Global Oncology Value Access & Pricing will both develop and ... access strategy for the assigned oncology asset(s). This person will report to the Sr Director, Global Oncology Value Pricing & Access, and will be responsible for… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …personal development. Are you ready to realize your potential? The Position The Senior Application Architect leads the team of skilled technical experts to design, ... solution until the issue is fixed. Relationships This position reports to Associate Director of Web Technology Platform Development and Operations in Information… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …of research and strategic partnership contracting agreements. In collaboration with the Associate Director, the Associate Manager will support CMR's partnership ... internal and external stakeholders Relationships This position reports to an Associate Director overseeing the contract management function of the CMR organization.… more
- Novo Nordisk Inc. (Boulder, CO)
- …cost & timely completion of all validation deliverables. Relationships Associate Director. Essential Functions Perform, review & approve validation/revalidation. ... & approve validation procedures, specifications & quality documents for accuracy & compliance Presentation & support for validation concepts & approaches with audits… more
- Eisai, Inc (Nutley, NJ)
- …to the Senior Director, Omnichannel Marketing (HCP and Patient). The associate director will also partner closely with key internal partners to deliver ... omnichannel and media specific marketing input and activities.The Associate Director of Omnichannel Marketing and Media is responsible for managing, executing and… more
- Merck & Co. (Millsboro, DE)
- …Delaware seeks to add an Attending Veterinarian in the role of Associate Director.This position will have overall responsibility for oversight and administration of ... at our company's Millsboro Animal Health facilities. This role is highly compliance -driven in accordance with State and Federal regulations as applicable to the… more
- Merck & Co. (Rahway, NJ)
- …environmental impact and advancing sustainability across its global operations. The Associate Director, renewable energy and carbon offset procurement lead will be ... engagement, and stakeholder management, you will collaborate with cross-functional teams, senior stakeholders and our supplier network. You will lead the category… more
