- Merck & Co. (Rahway, NJ)
- …and enable innovation.We are looking for an experienced professional with a strong IT - Product Management background to help us shape the vision and strategy of ... work experience, with at least 3+ years of demonstrated Technical Product Management experience supporting Information Technology, Pharmaceutical Research,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Scientist, Device Risk Management Lead , is a crucial member of our team, responsible for spearheading risk management efforts in ... combination product development, commercialization, and lifecycle management . This individual will oversee device risk management... Management will be responsible for device risk management activities in the following aspects: Lead … more
- Merck & Co. (Rahway, NJ)
- …years of relevant work experience, with at least 5+ years in Technical Product Management supporting IT applications or technology solutions. Strong experience ... how we engage internal and external audiences. Key Responsibilities Product Strategy & Roadmap: Lead and manage... Management Process, Management System Development, Product Development, Product Management , … more
- Merck & Co. (Rahway, NJ)
- Job DescriptionSr. Principal Scientist - Device Technical and Engineering Lead (Sr. Director Equivalent)Our company's Device Product & Process Development (DPPD) ... to positively support and influence clinical and commercial combination product development and launches.Principal Responsibilities: Lead and set direction… more
- Genmab (NJ)
- …Domestic travel of > 50% will be required.Responsibilities The Director, HEOL Team Lead is responsible for the management of the HEOL team including:Ensure ... RoleGenmab is currently seeking a Director, HEOL (Health Evidence and Outcomes Liaison) Team Lead to be a part of an exciting, passionate, high profile, high impact… more
- Insmed Incorporated (NJ)
- …future of science, we're in. Are you?About the Role:The Global Regulatory Lead (GRL) will be responsible for formulating and implementing global regulatory ... strategies and plans to enable efficient, competitive product development for assigned programs. This role will provide...activities. The GRL will serve as the global regulatory lead for documentation review prepared by other technical functions… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QA Investigations Lead I as part of the Quality team based in Raritan, NJ. Role ... OverviewThe QA Investigation Lead is an exempt level position reporting to the...occur in the production of a personalized cell therapy product in a sterile GMP environment. The ideal candidate… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …customers. Our passion for helping people live better lives and our award-winning product pipeline can only be as effective as our ability to provide information ... need them most, by creating an environment where innovation and chronic disease management drive optimal health outcomes. Are you ready to realize your potential?… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …for evaluation of changes to the same and their impact on the Carvykti product . Stakeholder management is required to drive and implement documentation template ... the treatment of multiple myeloma.Legend Biotech is seeking Validation Lifecycle & Technical Lead as part of the Global MSAT team based in Remotely. Role… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QA Investigations Lead III as part of the Quality team based in Raritan, NJ. Role ... OverviewThe QA Investigations Lead is responsible for providing quality oversight over the...of quality metrics while ensuring high quality and complaint product supply.Key Responsibilities Support compliance activities for site Quality… more
