- Merck & Co. (Rahway, NJ)
- …and final approval for all submissions and associated documentation. Provide expertise as the Global Regulatory Lead to Product Development Teams and the ... Job DescriptionThe Director / Principal Scientist, Regulatory Affairs Liaison , is...agencies for multiple indications simultaneouslyProvide expert advice as the Global Regulatory Lead to Product Development… more
- Merck & Co. (Rahway, NJ)
- …Clinical Manufacturing, Compliance Reviews, Data Analysis, Decision Making, Drug Product Manufacturing, Environment Health and Safety, Global Mindset, ... Job DescriptionAbout the Role:-As a Technical Lead, you will report into Director , Chemical Technical Operations, External Manufacturing API Technology, and play a… more
- Merck & Co. (Rahway, NJ)
- …compounds is a plus. New Product Introductions - Knowledge of Pharmaceutical product development and commercialization. Awareness of MDCP development and ... of lean principles, equipment design, and preventative maintenance.- Regulatory - Global regulations and compliance requirements governing development and… more
- Merck & Co. (Rahway, NJ)
- …compound(s)/ program(s). The incumbent must have demonstrated understanding of E2E product development process & connectivity between functions supporting ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for...supporting all protocol and program cost estimates requested by Product Development Teams.-Responsible for authoring clinical supply… more
- Merck & Co. (Rahway, NJ)
- … Development Division scientists, our Manufacturing Division and Animal Health product experts, global regulatory, controlled substances and others to enable ... DescriptionReporting to the Customs & International Trade (CIT) Tariff Classification Associate Director , the Senior Specialist will work closely with our Research &… more
- Merck & Co. (Rahway, NJ)
- … of drugs in our company's pipeline, with a deep understanding of product development from early stage through commercialization.Actively partnering with other ... communication to build trusting relationships.Applying a deep understanding of new product development and commercialization to analytical development … more
- Merck & Co. (Rahway, NJ)
- …Reporting to the Customs & International Trade (CIT) Valuation Associate Director , the Senior Specialist position's core responsibilities are to oversee our ... Company's Global Value for Customs Purposes (VCP) program and conduct...issues, on an as needed basis.Responsibilities Contribute to the development and maintenance of customs valuation standards and procedures… more
- Merck & Co. (New York, NY)
- …are seeking a Growth and Improvement minded Oncology Regional Medical Scientific Director that can help drive our Strategic Operating Priorities. Invent-- Pursue the ... must reside in the territory.Strategic Summary The Oncology Regional Medical Scientific Director is a credentialed (ie, PhD, PharmD, DNP, MD) oncology expert who… more
- Formation Bio (New York, NY)
- …to lead all Chemistry, Manufacturing, and Controls (CMC) activities related to biologic product development at Formation Bio. This is a strategic and ... clinical, and commercial-stage biologic products, ensuring alignment with company goals and global regulatory standards. Team Development Build and lead a… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. SummaryThe Executive Director , Head of Center of Excellence (CoE), Global Medical Safety ... diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi...across various regions, offering guidance and support to each product safety team in critical areas such as individual… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and immune disorders. Job Summary: The Senior Director sits within Global Oncology Clinical Development , an organization dedicated to the effective strategy, ... of AEs, medical history, and medications when needed Clinical Development Expertise Strategy:In collaboration with the Global ...consistent with CDP and aligned to achieve the Target Product Profile (TPP) Development of clinical sections of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …programs to the highest quality standards. This position reports to the Head, Global Development and Medical Affairs QA RDPVQA, and oversees multiple levels ... around rare diseases and immune disorders. JOB SUMMARYThe Senior Director , Head Medical affairs Quality Assurance in Global...ensure relevant quality reports and or assigned by Head, Global Development and Medical Affairs QA delivered… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …this role may function as a key member of the Global Product Team in collaboration with Clinical Development , Regulatory, Project Management, Biostatistics, ... and review of team output cross-functionally.- Effectively represent the CSPV on the Global Product Team or specific sub-teams such as clinical study team… more
- Daiichi Sankyo, Inc. (New York, NY)
- …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... Territory Managers and is accountable for the compliant promotion of the assigned product with the assigned customers. This territory covers the following states NJ… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... with some supervision. This position contributes to specific aspects of drug development plans with minimal supervision and contributes to documents submitted to… more
- Eisai, Inc (Nutley, NJ)
- …responsible for development of global regulatory strategic plans for new product development , as well as life cycle management of existing products. May ... regulatory/business objectives. The Executive Director will direct the development and submission of investigational drug applications, product registration… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …strategies by integrating the voice of the consumer into all levels of product development and marketing initiatives to ensure an enhanced user experience ... future. Our culture is centered around collaboration, connection, ownership, and development . We're a people-centered team doing patient-centered work - if you're… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …design pull you in? Are you ready to experiment with us? The Position The Director Channel Strategy & Planning will play a critical role in shaping the future ... brand leads. Essential Functions Integrated Portfolio Strategic Planning o Lead the development and operationalization of the Brand portfolio strategy for in line… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …SPC Leadership Team members, and acts as back up support for Executive Director Contract Development o Manages Contract Managers responsible for authoring ... Nordisk, you will have the opportunity to build a life-changing career in a global business environment. We encourage our employees to make the most of their talent,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Nordisk, you will have the opportunity to build a life-changing career in a global business environment. We encourage our employees to make the most of their talent, ... hard work and dedication with opportunities for continuous learning and personal development . Are you ready to maximize your potential with us? The PositionThis… more
