- Merck & Co. (Rahway, NJ)
- …to GCS and serve s as the lead GCS spokesperson at clinical and development related meetings.- Working independently, the Program CSPM designs strategic and ... key partner organizations ( as a lead GCS Planning program representative ) such as clinical development ,...Planning program representative ) such as clinical development , regulatory, quality and other supply chain areas to… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …& Market Access teams to ensure the design and execution of high-impact program strategies that support patients Support development of communication and ... reward hard work and dedication with opportunities for continuous learning and personal development . Are you ready to maximize your potential with us? The Position… more
- Merck & Co. (Rahway, NJ)
- …laboratory / regulatory documentation. Active strategic and technical leadership on program development teams, interfacing with key stakeholders, and ... Job DescriptionThe Mixed Modalities team within Sterile Product Development is responsible for developing parenteral dosage forms (injections, implants, inhaled,… more
- Merck & Co. (Rahway, NJ)
- …independently with minimal supervision and/or lead QP2 efforts on drug/vaccine development programs, and author or co-author strategic documents. Associate ... and Pharmacometrics (QP2) department drives model-informed drug discovery and development (MIDD) to routinely enable efficient drug discovery/ development … more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …accredited school program to be eligible to apply* The L&D Associate helps in the creation, administration, organization and presentation of company trainings, ... of this role include supporting the creation of learning and development initiatives and programs, assisting with, and scheduling learning opportunities. Job… more
- Aequor (Thousand Oaks, CA)
- …role is a 100% onsite, lab-based position, supporting the oligonucleotide (oligo) program with a focus on synthetic small molecules. The ideal candidate holds ... Provide and present results to support drug substance and drug product development . - Transfer analytical methods to contract manufacturing or contract testing labs.… more
- Novo Nordisk Inc. (Durham, NC)
- …The Position Responsible for supervising the validation, maintenance and calibration program for QC laboratory instrumentation. Ensures timely execution of the ... Manager. Essential Functions Ensure QC validation, equipment maintenance and calibration program is executed timely Coordinate with the responsible manager and other… more
- Aequor (Devers, TX)
- Bio-Process Associate , 2nd Shift100% Onsite in Devens, MA6 Months contract - With high possibilities of Extension Job Responsibilities:Operates control systems and ... machinery, or physical presence in a laboratory, research, drug development , or manufacturing facility are prohibited from having any...fit for all the duties of the job. Training Program :Selected candidates will be required to enter a structured… more
- Insmed Incorporated (Phoenix, AZ)
- …and HCP experience "post prescription" is the exact vision of the Insmed Patient Support Program and the reason we are seeking top talent for the role of ... Associate Director, Patient Support Specialist Team. Patients are the...purposeful, in-person engagements.ResponsibilitiesDeliver upon an industry leading Patient Support Program with leadership of a Patient Support Specialist Team.Key… more
- Merck & Co. (Millsboro, DE)
- …external regulatory inspections (USDA, DEA, DNREC, etc.) of animal facilities and program reviews is required.PurposeThis Associate Director will report to the ... Job DescriptionOur company seeks to add an Associate Director. Veterinarian Services at our Millsboro, Delaware...well as for the veterinary care and animal husbandry program at our company's Millsboro Animal Health facilities. This… more
- Merck & Co. (Rahway, NJ)
- …CCFS supports various commercialization activities, second generation process development including process characterization, technology transfer to internal and ... partners, this individual will support late stage and commercial large molecule program activities within CCFS. The individual will be responsible for leading a… more
- Merck & Co. (North Wales, PA)
- …Sciences), a distinguished department within our renowned Research and Development division, quantitative scientists, in partnership with other subject matter ... state-of-the art scientific methodologies and tools to enable the discovery, development , regulatory approval, manufacturing, and marketing of medical drugs and… more
- Merck & Co. (Rahway, NJ)
- …strategies for innovative combination products?Join our company's Device Product & Process Development (DPPD) Team, which focuses on the design, development , and ... delivery to their intended sites of action. The DPPD Team oversees the development of the device constituent within our pipeline of combination products, spanning… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAssociate Principal Scientist, Small Molecule Analytical Research & Development --The Small Molecule Analytical Research and Development (SMAR&D) ... group has an exciting opportunity for an Associate Principal Scientist based in Rahway, NJ. Join us...Pipeline: Leading or participating on analytical teams driving the development of drugs in our Company's pipeline, with a… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Vice President (AVP) will be responsible for leading the Translational Medicine (TMed) Cardiovascular & Respiratory Therapeutic Area and ... strategy, bridging the continuum from Discovery Research through Late-Stage Clinical Development .- The AVP provides strategic oversight for the early clinical space,… more
- Merck & Co. (Rahway, NJ)
- …to join the Global Safety Center of Excellence (CoE) team as an Associate Director, Safety Programs CoE.- This individual will be responsible for the management ... control safety hazards for manufacturing, research and office personnel.Conduct safety program reviews at company facilities across the globe.Audit safety records… more
- Merck & Co. (Rahway, NJ)
- …journey to become the premier "Data First" commercial biopharma organization.In this Associate Director Data Product Management role, you will be part of the ... data product, including use case identification, discovery all the way to development and maintenance.Knowledge about specialty products, SP and Hub data and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Chemical Engineering Research & Development department (CERD), part of the Process Research and Development organization, is seeking a highly ... with applications in microbial fermentation operations and downstream bioprocess development to support manufacturing of enzymatic catalysts for small molecule… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- Legend Biotech is seeking Associate Technical Lead as part of the Technical Operations team based in Raritan, NJ. Role OverviewThe Associate Technical Lead will ... according to cGMP requirements. This individual will support the hiring and development of Manufacturing Excellence associates. This individual will also own the… more
- Genmab (Plainsboro, NJ)
- …Provide line management for CTMs and CTAs across trials within a program , ensuring performance and competency development .Collaborate with Global Clinical Trial ... CTAs.Advise on resource needs and team performance to support overall program resource planning.Ensure team success through setting clear expectations, guiding… more
