- Merck & Co. (Rahway, NJ)
- …management and operation support. The Associate Director of Biologics Process Research and Development (BPR&D) is responsible for supporting Biologics ... Process Development (BPD)'s lab maintenance and operations. This includes maintaining...lab equipment preventive and corrective maintenance (PM/CM). The US Associate Director is also responsible for leading… more
- Merck & Co. (Rahway, NJ)
- …corporate priority and expected to be a key growth driver for our company.The Associate Director , Healthcare Consumer (HCC) / Patient Strategy - Global Marketing ... broadly with cross-functional partners to support enterprise-wide commercialization preparedness.--The Associate Director will play an important role in… more
- Merck & Co. (Rahway, NJ)
- …the design and implementation of cutting-edge data solutions. - As the Associate Director - Technical Product Manager for the Cross-Divisional Marketplace ... company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director of Method Development & Testing is responsible for leading a Center of Excellence (CoE) focused on developing and ... GMP testing nodes in support of clinical and PPQ supplies. Additionally, the Associate Director leads, manages, and develops a team responsible for providing… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Associate Director , Clinical Scientist This position drives scientific planning, strategy and execution of Phase 1-4 ... of clinical data/medical protocol-deviations in collaboration with the Clinical Director .Builds talent and capabilities of direct and indirect team members… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Office of General Counsel is seeking an Associate Director , Legal - Intellectual Property (IP) Technology & Operations to provide application ... management system and create custom rules and codes Design and deliver new process workflows or data-related projects and other process improvements Design and… more
- Merck & Co. (Rahway, NJ)
- …healthcare. The Biologics and Biopharmaceutics team is responsible for the research and development of sterile & parenteral drug products for biologics as well as ... oral and non-oral portfolio. Within Biologics and Biopharmaceutics, the Biopharmaceutics Director will influence the strategy, lead activities, and develop a team… more
- Merck & Co. (Rahway, NJ)
- …drug product team that designs and executes experiments to support formulation and process development and document technical reports and regulatory filings. The ... seeking a highly motivated candidate for the position of Director , Small Molecule Development within the Mixed...results on firm deadlines in support of product discovery, process development , and commercial filings for biopharmaceuticals… more
- Merck & Co. (Rahway, NJ)
- …labeling and obtain shortest time to approval by global regulatory agencies.Reports to Associate Vice President, Executive Director , or Senior Director in ... Job DescriptionWe are seeking a Director (Principal Scientist), Global Regulatory Affairs Liaison with...Principal Scientist - Regulatory Affairs Liaison is responsible for development and implementation of worldwide regulatory strategy for their… more
- Merck & Co. (Rahway, NJ)
- …Safety (GRACS) and external to GRACS. Key Functions Reports to Executive Director or Associate Vice President, General MedicineWorks Independently and as ... Job DescriptionWe are seeking a Senior Director (Sr. Principal Scientist) Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can help… more
- Merck & Co. (Rahway, NJ)
- …top corporate priority and expected to be a key growth driver for our company.-The Associate Director of Global Marketing for a first- in - class treatment will ... and manufacturing, medical affairs, Outcomes Research and Access.Understanding of Drug Development Process (Early and Late Stage).Strategic Thinking: Proven… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …multidisciplinary pharmaceutical /diagnostic development teams.Understanding of the IVD Development Process , with indirect or direct experience with ... and new assay technologies such as NGS, IHC, PCR etc.Knowledge of drug development process and an understanding of how diagnostic development can shape drug… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …implement effective regulatory strategies to deliver on efficient and robust development plans. The individual will direct, coordinate and implement the preparation ... regulatory agencies receive timely and quality submissions, shortening the review process and leading to successful approval of pharmaceutical applications for the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …problems.Serve as a liaison between the customer community and the software development team, documenting functional, system, and process requirements.Possess a ... rare diseases and immune disorders.Summary Responsible for managing the design, development , optimization and administration of global HCM Platforms and processes.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …preferred- 4 or More Years Extensive experience in project management, process , product, and/or analytical development activities and pharmaceutical/oncology ... defined based on the project needs and the respective development stage of the project. The CMC Lead will...Participate in cross-functional teams responsible for regional and global process improvements in the operational efficiency of PJ Lead… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. SummaryThe Associate Director , Global Medical Affairs (GMA) Oncology- Medical Content ... is responsible for execution of global scientific and training deliverables. The Associate Director develops and executes Medical Content and Training plans… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Summary The Associate Director Global Oncology Strategic Planning provides strategic insights ... launched brands. The role will be responsible for the development and maintenance of Short to Long Term Forecasts...and Strategic input into the annual R&D Pipeline prioritization process to ensure DS's R&D resources are appropriately invested.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders.Job Summary Deliver the development and implementation of informatics systems and programs to support the ... global sites. These business functions include: Clinical Operations, Clinical Development , Biostatistics and Data Management, Regulatory Affairs, Quantitative Clinical… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Provides support to the portfolio or operating budget and/or resource prioritization process and serve as global coordinator with activities with Japan (forecast ... and Forecasting - Manages and is accountable for the development and control of Clinical Project Budget in support...and new pipeline studies in support of the annual process of extracting the optimal value out of our… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Reinforces labeling best practices at cross-functional meetings. Assists in the development of Standard Operating Procedures (SOPs) and process improvements. ... including post marketing projects and those involving 3rd party development . This position partners with GRLs and Clinical Safety...may assist another Global Labeling Lead by managing labeling development or approval for either the US or EU.… more
