- Eisai, Inc (Nutley, NJ)
- …difference. If this is your profile, we want to hear from you. The Associate Senior Counsel, Privacy, is a strategic, business-minded, and hands-on attorney role ... In expanding and managing Eisai's US Privacy Program, the responsibilities of the Associate Senior Counsel, Privacy, include, but are not limited to, practical… more
- Aequor (West Greenwich, RI)
- …within bulk drug substance operations adhere to cGMP and other regulatory requirements. Key Responsibilities: Provide quality oversight for F&E, IQA Warehouse ... materials, processes, and products comply with cGMP standards and other applicable regulatory requirements. Review and approve work orders and job plans within… more
- Insmed Incorporated (San Diego, CA)
- …the future of science, we're in. Are you?About the Role:Insmed is seeking a Senior Research Associate - Lab Technician with specialized expertise in supporting ... and interpret experimental data, contributing to reports, presentations, and regulatory documentation.Maintain accurate electronic laboratory notebooks and ensure adherence… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …position, task oriented in the execution of processes, as directed by senior staff, playing a supportive role in ensuring adherence to Project objectives, ... and GCPs and is compliant with domestic and foreign regulatory requirement but may seek support on such items...working environment as well as Quality Assurance and global regulatory requirements such that identification of risks is recognized… more
- Aequor (Thousand Oaks, CA)
- …Facing SKU Change Records (CFSCR) Provide timely updates to stakeholders, eg, Regulatory , Supply Chain, Manufacturing, Quality on status of GDCR and/or CFSCR ... directionBasic Qualifications Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED… more
- Merck & Co. (Rahway, NJ)
- …development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director ... Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility...closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development… more
- Insmed Incorporated (NJ)
- …and for the future of science, we're in. Are you?About the Role:The Associate Director, Medical Review Committee (MRC) Operations is responsible for managing the ... operational execution of the company's Global We're looking for an Associate Director, Medical Review Committee Operations, on the Medical Review team to help us… more
- Merck & Co. (Rahway, NJ)
- …DescriptionAssociate Principal Scientist - Device Technical and Engineering Lead ( Associate Director Equivalent) Our company's Device Product & Process Development ... products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements.-This position will lead cross-functional… more
- Insmed Incorporated (NJ)
- …future of science, we're in. Are you?About the Role:We're looking for an Associate Director, IT Marketing Technologies, on the Information Technology team to help us ... expand what's possible for patients with serious diseases. Reporting to the Senior Director, Global Data Enablement, Corporate & Commercial Reporting, you'll serve… more
- Novo Nordisk Inc. (Boulder, CO)
- …of both worlds to develop new medicines for patients. The Position The Associate Director of Drug Product Manufacturing is accountable for all clinical drug product ... meeting patient and business needs Rapidly and accurately communicate issues to Senior Leadership. Resolve manufacturing and facility issues to mitigate any supply… more
