- Merck & Co. (Rahway, NJ)
- …molecule and synthetic modality pipeline.The Director will report to the Executive Director of Sterile Product Development - Mixed Modalities, and lead a ... and inclusive work environment.Essential Knowledge, Duties & Responsibilities for the Director Include:Sterile drug product development concepts, tools, and… more
- Merck & Co. (Rahway, NJ)
- …(IP) Technology & Operations to provide application administration and technology management support to the Intellectual Property (IP) organization.Primary ... departmental IT risk management policies and practices Intellectual property (IP) Technology Management Design and implement a long-term technology … more
- Merck & Co. (North Wales, PA)
- Job DescriptionOur Company Information Technology organization partners with colleagues across the business to help serve our patients and customers around the ... contribution to global medical innovation by leveraging information and technology .-One of the key priorities for our Company is...drives results.Reporting to the HH IT US Data Services Product Line Leader, this role will be responsible for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Summary The Associate Director , Program Management is a senior position responsible for effectively ... of people globally by leveraging our world-class science and technology . With more than 100 years of scientific expertise...functions in Daiichi Sankyo (DS). Reporting to the Sr. Director , Enterprise Program Management , this position requires… more
- Merck & Co. (Boston, MA)
- …targeted delivery, or modification of molecule release.Strong Leadership and Team Management Skills: The Director should possess strong leadership qualities ... on candidate molecules, and influence broader research initiatives.Budget and Resource Management : The Director should have experience in planning, preparing,… more
- Tris Pharma (Monmouth Junction, NJ)
- …many departments across all stages of the product lifecycle. The Associate Director , Alliance Management will be accountable for managing alliances of high ... have an immediate opening in our Monmouth Junction, NJ facility for an Associate Director , Alliance Management .Tris Pharma has a long track record of successful… more
- Tris Pharma (Monmouth Junction, NJ)
- Associate Director / Director , Analytical Research and DevelopmentMonmouth Junction, NJ Analytical Development, R&DDescriptionTris Pharma, Inc. ... spanning neuroscience and other therapeutic categories employing our proprietary science and technology .Our science and technology make us unique, but it is… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …unmet medical needs of people globally by leveraging our world-class science and technology . With more than 100 years of scientific expertise and a presence in ... areas centered around rare diseases and immune disorders.Summary: The Associate Director , Regional Marketing Conventions & Field Programs will be responsible for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …unmet medical needs of people globally by leveraging our world-class science and technology . With more than 120 years of scientific expertise and a presence in ... plans for specific categories under the direction of the head of category management , for the creation, execution, tracking of strategies. Includes working under a… more
- Merck & Co. (Rahway, NJ)
- …adherence to quality standards and regulatory requirements throughout the product design, development, and manufacturing processes.Implement risk management ... Job DescriptionThe Executive Director , Device Quality & Regulatory will play a...with external partners, suppliers, and regulatory bodies to support product launches and lifecycle management .Education: Bachelor's Degree… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …R&D, Project Management and Quality Control departments to complete the technology transfer for customers. This position will lead, mentor and grow the Technical ... Position SummaryThe Sr. Director of Technical Transfer is responsible for activities...tasks related to process development, scale-up, process optimization, customer technology transfer activities with project management assistance.Provide… more
- Merck & Co. (North Wales, PA)
- …experience.- Experience Required: At least five years of experience in technology implementation, business process improvement, project management , systems ... a premier research-intensive biopharmaceutical company. We are seeking an Associate Director , Clinical Systems Implementation to manage activities related to the… more
- Merck & Co. (Rahway, NJ)
- …updates.Supports device sites with the collection and analysis of data for management review. Reports to - Director Regulatory Compliance, Device Quality ... Job DescriptionPosition Title - Director / Principal Scientist, Regulatory Compliance Department - Device...regulations, final guidance and standards.Provide strategic advice to senior management on CMC regulatory matters based on health authority… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- Director , Clinical Development Join a Legacy of Innovation 125 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of innovative ... unmet medical needs of people globally by leveraging our world-class science and technology . With more than 125 years of scientific expertise and a presence in… more
- Tris Pharma (Monmouth Junction, NJ)
- …spanning neuroscience and other therapeutic categories employing our proprietary science and technology .We truly believe that to innovate and to set us apart, we ... from you.We are hiring at our Monmouth Junction NJ Headquarters for a Senior Director to lead our small, but productive, Marketing team.The Senior Director , Head… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …early-stage programs, in order to proactively perform safety surveillance and risk management in partnership with Product Safety Lead(s), Clinical Safety ... the PSL(s) to proactively plan and prioritize safety surveillance and risk management activities for assigned product (s), including resource planning, oversees… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …unmet medical needs of people globally by leveraging our world-class science and technology . With more than 100 years of scientific expertise and a presence in ... areas centered around rare diseases and immune disorders.Summary The Senior Director sits within Global Oncology Clinical Development, an organization dedicated to… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …unmet medical needs of people globally by leveraging our world-class science and technology . With more than 120 years of scientific expertise and a presence in ... areas centered around rare diseases and immune disorders. SummaryThe Senior Director sits within Global Oncology Clinical Development, an organization dedicated to… more
- Daiichi Sankyo, Inc. (Seattle, WA)
- …unmet medical needs of people globally by leveraging our world-class science and technology . With more than 100 years of scientific expertise and a presence in ... areas centered around rare diseases and immune disorders. Summary: The Associate Director , Field Reimbursement (ADFR) is a critical front-line member of the DSI… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …unmet medical needs of people globally by leveraging our world-class science and technology . With more than 100 years of scientific expertise and a presence in ... Regulatory Affairs (GRA) Labeling Strategy expert to the Global Product Team (GPT) as an ad hoc member and...through all labeling discussions with the FDA/CHMP while ensuring management alignment. Strategize and plan for FDA meetings as… more
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