- Merck & Co. (Rahway, NJ)
- …under their direction within the framework of Company policy.Collaborates effectively with Process Chemistry , Discovery Process Chemistry , Enabling ... Job DescriptionReports to the Executive Director of External Capabilities, Small Molecule Process...to provide strategic direction and innovative solutions to synthetic chemistry and development problems to ensure successful API deliveries… more
- Merck & Co. (Rahway, NJ)
- …Operations Specialist role at the Associate Specialist level will serve as a process team member supporting the Modality Agnostic Chemistry Scaleup (MACS) ... The MACS Operations Specialist position will report to the Director , Engineering and will be a member of the...support new and/or existing facilities across the Small Molecule Process Research & Development (SM PR&D) network. -As the… more
- Merck & Co. (Rahway, NJ)
- …responsible for building and executing CMC development plans.Under the guidance of the Director & Portfolio Lead, the core responsibility of this individual will be ... to lead project management efforts to support Chemistry Manufacturing & Controls (CMC) product development from First...product development from First in Human to Transfer to Supply , driving line of sight across the development lifecycle… more
- Merck & Co. (Rahway, NJ)
- … supply manufacture of our Company's drug product pipeline.- The FLEx Sterile Process Engineer at the Associate Director level serves as a technical subject ... FLEx Sterile Process Engineering Lead in Pharmaceutical Operations & Clinical Supply .- Primary Responsibilities: Serve as a technical expert and mentor to a team… more
- Merck & Co. (Rahway, NJ)
- …pad for the early phase and commercial formulation development and GMP clinical supply manufacture of our Company's drug product pipeline.- The FLEx Process ... of the FLEx Center.- They will be responsible for developing equipment and process subject matter experts who will partner with formulators and device engineers to… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …110 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address ... to meet smooth transition with other sub projects with respect to supply , product quality and stakeholder satisfactions. Responsible to communicate and escalate to… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Executive Director , Device Quality & Regulatory will play a pivotal leadership role within the organization, overseeing the quality assurance and ... to commercialization. The individual will also manage the regulatory Chemistry , Manufacturing, and Controls (CMC) content for global submissions, ensuring… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …110 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address ... an accredited college or university)Bachelor's Degree Degree required in chemistry , biochemistry, pharmaceutics or related discipline within the pharmaceutical/biotechnology… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …110 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address ... regulatory agencies receive timely and quality submissions, shortening the review process and leading to successful approval of pharmaceutical applications for the… more
- Novo Nordisk Inc. (Boulder, CO)
- …With a new laboratory completed in 2021 to support analytical and process development, the CMC team works alongside Quality, Regulatory, Technical Operations and ... multiple projects. The position will work with CMO's to ensure the continuous supply of product and apply risk mitigation strategies, as well as perform formulation… more
- Merck & Co. (Rahway, NJ)
- …project management responsibility. The Specialist -Engineering position will report to the Associate Director , Engineering and will be a member of the EF Team at the ... The SSO is a Good Manufacturing Practice (GMP) manufacturing facility in the Process Research and Development (PR&D) organization.- The pilot plant's mission is to… more
- Merck (Rahway, NJ)
- …under their direction within the framework of Company policy. Collaborates effectively with Process Chemistry , Discovery Process Chemistry , Enabling ... **Job Description** Reports to the Executive Director of External Capabilities, Small Molecule Process...to provide strategic direction and innovative solutions to synthetic chemistry and development problems to ensure successful API deliveries… more
- Merck (Rahway, NJ)
- …Operations Specialist role at the Associate Specialist level will serve as a process team member supporting the Modality Agnostic Chemistry Scaleup (MACS) ... The MACS Operations Specialist position will report to the Director , Engineering and will be a member of the...support new and/or existing facilities across the Small Molecule Process Research & Development (SM PR&D) network. As the… more
- Organon & Co. (Plymouth Meeting, PA)
- …in Organon Regulatory CMC New Products, the Associate Principal Scientist (Associate Director ) is responsible for Regulatory Chemistry Manufacturing & Controls ... limited to: **Responsibilities** + Partner with Research & Development, Manufacturing & Supply , Business Development and Commercial to embed an adaptable process … more
- Merck (Rahway, NJ)
- …for building and executing CMC development plans. Under the guidance of the Director & Portfolio Lead, the core responsibility of this individual will be to ... lead project management efforts to support Chemistry Manufacturing & Controls (CMC) product development from First...product development from First in Human to Transfer to Supply , driving line of sight across the development lifecycle… more
- BeiGene (San Mateo, CA)
- …has global responsibility and accountability for commercial product quality for global supply . The job holder leads and develops a staff of Quality professionals ... to oversee commercial product on the end to end supply chain. The job location could be in US,...commercial product quality team to ensure the quality management process is in place and executed to ensure the… more
- Lilly (Indianapolis, IN)
- …who are determined to make life better for people around the world. The Associated Director of the Joint Process Team (JPT) is responsible for leading a cross ... are delivered on time and within downstream customer expectations. The JPT Associate Director will partner with Lilly's Process Research & Development group on… more
- Merck (Rahway, NJ)
- …pad for the early phase and commercial formulation development and GMP clinical supply manufacture of our Company's drug product pipeline. The FLEx Process ... of the FLEx Center. They will be responsible for developing equipment and process subject matter experts who will partner with formulators and device engineers to… more
- Merck (Rahway, NJ)
- … supply manufacture of our Company's drug product pipeline. The FLEx Sterile Process Engineer at the Associate Director level serves as a technical subject ... FLEx Sterile Process Engineering Lead in Pharmaceutical Operations & Clinical Supply . **Primary Responsibilities:** + Serve as a technical expert and mentor to a… more
- Lilly (Lebanon, IN)
- …organization provides technical oversight to ensure robust and consistent biology and chemistry throughout all aspects of the manufacturing process . Through ... ensures the quality and safety of our products through process monitoring and knowledge to control, prevent and mitigate...control, prevent and mitigate variability to deliver a reliable supply of medicine. The Associate Director is… more
