- Aequor (Thousand Oaks, CA)
- …floor. Detail Oriented, Team player and Quality Experience. The Sr. Associate Quality Assurance position supports 's Quality Assurance program under the ... manufacturing areas. Under general supervision, the role provides support and compliance oversight to Manufacturing and Facilities and Engineering staff in 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
- Aequor (Thousand Oaks, CA)
- …manufacturing areas. Under general supervision, the role provides support and compliance oversight to Manufacturing and Facilities & Engineering areas/staff in the ... minor deviations and CAPA records. Responsibilities will include evaluation of compliance issues, providing recommendations, and assuring progress of quality records… 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
- 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
- Insmed Incorporated (Bridgewater, NJ)
- …while adhering to corporate policies and external regulations and guidance. The Senior Manager, Scientific Communications & Publications, provides support to the ... Associate Director/Director for the development and execution of the...medical experts, investigators, publishers, and publication support vendors/agencies. The Senior Manager, Scientific Communications & Publications drives the timely… 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
- Merck & Co. (Durham, NC)
- Job DescriptionPosition Description: Senior Specialist, Manufacturing Automation The Senior Specialist Manufacturing Automation person is primarily responsible ... to improve manufacturing performance, and maintaining the automation systems in compliance with cGMPs. The Manufacturing Automation Sr. Specialist must actively… more
- American Honda Motor Co Inc (Marysville, OH)
- …assist and support the North American Regional Operating Board (NAROB) and senior executives across North America to strengthen risk management, internal controls, ... Audit also promotes self reliance within NA operations and ensures regulatory compliance while maintaining competitive costs but with the highest quality and… more
- Merck & Co. (North Wales, PA)
- …Hybrid work model (combination of in-office and work from home abilities).The- Associate Director, Digital & Omnichannel Innovation for US Oncology-focuses on digital ... teams in order to build partnerships and trust with Commercial Legal, Compliance , Privacy and Regulatory colleagues to effectively alleviate concerns and mitigate… 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
- 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
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Regional Associate Director New Segments Development LatAm Main Objective: As the Regional Associate Director, your primary ... stakeholders across multiple divisions, countries, and regions.Strengths in influencing senior leaders, both internally and externallyBe resourceful, a self-starter… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …US and CA Clinical Trial sites. Accountable for overall performance management of Senior Supply team, who contribute to the planning, execution and spend of ... (eg Investigators and site staff, vendors etc.). Establish and manage senior level relationships positively with multiple internal stakeholders relevant to the… 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. (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
