- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or ... span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of late-stage clinical development and… more
- Merck & Co. (Rahway, NJ)
- …portfolio. Within Biologics and Biopharmaceutics, the large molecule product development Director will influence the strategy, lead activities, and develop a team ... whose roles include design and development of formulation, manufacturing process , and primary packaging to enable phase appropriate regulatory filings for large… more
- Merck & Co. (Durham, NC)
- …compliance.Support the Master Data team with general Material Handling Steward tasksDrive safety , quality and process enhancements throughout the supply chain - ... a wide range of business activities.- Reporting directly to the Director , Supply Chain Management, the successful candidate's primary responsibilities will include… more
- Merck & Co. (Rahway, NJ)
- …Practice (GMP) clinical supply manufacturing facility in Rahway, New Jersey.The Sterile Process Engineer role at the Associate Director level will leverage ... Phytochemistry, Process Control Automation, Process Optimization, Process Simulation, Product Formulation, Safety Compliance, Standard Operating… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAs a Technical Lead, you will report into Director , Chemical Technical Operations, External Manufacturing API Technology, and play a pivotal role in ... Ingredients (API) and intermediates. You will be responsible for providing process support, resolving production issues, evaluating process change requests,… more
- Insmed Incorporated (San Diego, CA)
- …lists.OverviewLead Analytical Development Operations function to build out the process development support testing function within analytical development. Will ... on a PDT as required by the business.ResponsibilitiesThe Analytical Development Operations associate director is responsible for building a team to take care of the… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJob Summary: -The Director , Combination Product Commercialization is a key leadership role within the Device Development and Technology Organization. ... with a focus on autoinjectors, prefilled syringes, and other drug delivery systems. The director will lead a team of engineers and technical staff to support global… more
- Merck & Co. (Rahway, NJ)
- …and accelerate process and product development and manufacturing and ensure safety and quality of our products. The successful candidate will be accountable for ... cross-functional development teams to enable pipeline decisions. -The Executive Director , Biologics Analytical Research and Development (B-AR&D) is responsible for… more
- Tris Pharma (Monmouth Junction, NJ)
- …in our Monmouth Junction, NJ facility for an experienced, hands-on SR. Director / Director , Procurement. Title and salary commensurate with experience. The ... Director / Senior Director , Procurement is responsible for...(FDA), Drug Enforcement Administration (DEA), and Occupational Health and Safety Administration (OSHA) regulations, as well as all applicable… more
- Genmab (NJ)
- …have you join us!The Global Regulatory Labeling, Policy and Intelligence Associate Director will primarily be responsible for leading the development and maintenance ... will be within Global Regulatory Affairs (GRA) and will report to the Sr. Director , Labeling, Policy and Intelligence. The position may be based in our Princeton,… more
- Eisai, Inc (Exton, PA)
- …If this is your profile, we want to hear from you. The Associate Director of Biologics Operations Upstream and Downstream is responsible for leading and building a ... technology transfer to external partners (as required). The Associate Director sets strategic directions and project priorities, providing scientific leadership… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …oversight groups for case processing activities and reports to the Director of PV Case Management.Responsibilities:ICSR Processing: Oversees QC activities, supports ... Reviews, approves, provides input on and authors SOPS, SOIs, and process guides. Participates in inspection preparation activities and internal and external… more
- Eisai, Inc (Nutley, NJ)
- …Management, Clinical Safety Data Review and Clinical team. The Assoc. Director of Clinical Programming will oversee the Data Review programming and JReview ... this is your profile, we want to hear from you. The Associate Director , Clinical Programming must have expertise in addressing technical challenges in the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …as R shiny apps for data surveillance, visualization, modeling and simulations, and safety signal detection. Lead the development and validations of R package and/or ... shiny apps. Identify and build the use cases and process /resources to guide the implementations. Lead, advocate and nurture R programming innovation globally within… more
- Merck & Co. (Durham, NC)
- …Operations, Drug Delivery Systems and Devices within our Manufacturing Division (Associate Director ).-This role serves as a Virtual Plant Manager - responsible for ... to deliver Pharmaceutical, Biologic, and Vaccine Products. Our team works with a " Safety First, Quality Always" mindset.-As the primary point of contact for all… more
- Merck & Co. (Rahway, NJ)
- …capital project scope and technical studies that support business objectives, with focus on Process Design and Process Safety for Small Molecule High ... Peer input during design, oversight during operation and development/implementation of Process Safety Initiatives. Up to 25% domestic/international travel… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …future capabilities. We're responsible for regulating accounting, upholding workplace safety , managing our supply chain and sampling, supporting technological and ... and they understand their level of accountability for results and the measurement process . Ensure that the IDP forms include completed learning and aspiration plans… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Summary: The Senior Director , Head of RBQM (Risk Based Quality Monitoring) sets the vision and ... risk factors with and for other technical departments (eg, Clinical, Medical, Safety , Data Management, Statistics). This position requires skills in working in a… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …future capabilities. We're responsible for regulating accounting, upholding workplace safety , managing our supply chain and sampling, supporting technological and ... analytics to senior stakeholders.Creative problem-solver with a track record of process improvement.The base compensation range for this position is $ 181,670… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Director (Principal Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed ... span all phases of clinical development (pre-clinical to post-licensure). The Director will manage the entire cycle of clinical development, including study… more
