- Aequor (Thousand Oaks, CA)
- …scientist to join the GCR - Process Excellence (GCR-PEX) team. This senior role balances advanced laboratory execution (cell culture, reagent generation and ... results into concise technical recommendations and present to cross-functional teams and senior stakeholders. Mentor and provide technical guidance to staff; act as… more
- Aequor (Thousand Oaks, CA)
- …lifecycle management knowledge of full product manufacturing stages experience. The Supply Chain Project Manager (SCPM) will translate product variation strategy as ... Records (CFSCR) Provide timely updates to stakeholders, eg, Regulatory, Supply Chain, Manufacturing, Quality on status of GDCR and/or...OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Years and Counting! Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address ... oriented in the execution of processes, as directed by senior staff, playing a supportive role in ensuring adherence...support in managing the forecasting and planning of drug supply needs. Can participate effectively on a cross functional… 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 ... technical summaries for internal and external stakeholders. Lab Management Oversee supply inventory, reagent ordering, and equipment maintenance to ensure continuous… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Years and Counting! Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good Clinical… more
- Aequor (West Greenwich, RI)
- …written procedures and cGMP requirements. Alert management of quality, compliance, supply and safety risks. Complete required assigned training to permit execution ... of required tasks. Responsible for being in clean room space for majority of time on shift which includes gowning in and out of frocks and coveralls. Communicating and collaborating with the PQA shift to ensure required tasks are completed Preferred… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across our company ... the Program CSPM designs strategic and operational plans for all clinical supply activities associated with the clinical studies in their assigned compound(s)/… more
- Cipla (Central Islip, NY)
- …working outside of Cipla's US Subsidiaries or Affiliates Job Title SCM Procurement- Associate Buyer Organization Name Invagen - A Cipla subsidiary Location New York, ... requirements. Identify, evaluate, and develop alternative vendors to diversify the supply base, mitigate risks, and ensure continuous supply . Conduct… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …125 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address ... other research areas centered around rare diseases and immune disorders. SummaryThe Associate Director Global Medical Affairs Oncology (GMA), under the direction of… 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 ... supporting multiple projects. The position will manage CMO's to ensure the continuous supply of product and apply risk mitigation strategies, as well as perform… more
