• Director RA, Global Labeling

    Integra LifeSciences (Princeton, NJ)
    …pathways to advance patient outcomes and set new standards of care. The Director , Global Regulatory Labeling is responsible for overseeing the prioritization, ... creation, review, approval, and maintenance of finished goods labeling artwork and templates. This role requires a solid...templates. This role requires a solid understanding of global labeling requirements, a basic understanding of labeling more
    Integra LifeSciences (11/08/24)
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  • Director Labeling

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …and immune disorders. **Summary** This position serves as the Global Regulatory Affairs (GRA) Labeling Strategy expert to the Global Product Team (GPT) as an ad hoc ... member and independently provides strategic and operational leadership on new product labeling in collaboration with the Global Regulatory Leads (GRLs) and Clinical… more
    Daiichi Sankyo Inc. (11/20/24)
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  • Director , Labeling

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …and immune disorders. **Summary** This position serves as the Global Regulatory Affairs (GRA) Labeling Strategy expert to the Global Product Team (GPT) as an ad hoc ... member and independently provides strategic and operational leadership on new product labeling in collaboration with the Global Regulatory Leads (GRLs) and Clinical… more
    Daiichi Sankyo Inc. (10/23/24)
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  • Associate Director , Global Regulatory…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …rare diseases and immune disorders. Summary This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic ... and operational leadership on product labeling in collaboration with Global Regulatory Leads (GRLs). This...hoc member of Global Project Team (GPT) to address labeling issues for late stage projects. This position manages… more
    Daiichi Sankyo Inc. (10/19/24)
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  • Associate Director Regulatory Affairs,…

    Ascendis Pharma (Princeton, NJ)
    …to working together as one team to achieve extraordinary results. The Associate Director Regulatory Affairs, Advertising and Promotion will be an internal expert on ... the promotion of prescription drug and biologic products. The Associate Director Regulatory Affairs, Advertising and Promotion is responsible for providing… more
    Ascendis Pharma (12/10/24)
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  • Director , Global Regulatory Leader (GRL)

    J&J Family of Companies (Raritan, NJ)
    Johnson & Johnson Innovative Medicine is recruiting for a Director , Global Regulatory Leader. This position can be located in Spring House, PA; Horsham, PA; ... potential. At Johnson & Johnson, we all belong. The Director , Global Regulatory Leader, is responsible for global regulatory...Regulatory Team (GRT): + Serve as a member of Labeling Working Group (LWG) to build or update the… more
    J&J Family of Companies (12/10/24)
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  • Senior Principal Scientist, Regulatory Liaison…

    Merck (Rahway, NJ)
    …and provides regulatory oversight for assigned products, to optimize product labeling and obtain shortest time to approval by global regulatory agencies. ... Respect | Inclusion + Develops worldwide product regulatory strategies to optimize labeling and obtain shortest time to approval by regulatory agencies for multiple… more
    Merck (12/13/24)
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  • Medical Director , Endocrine Medical…

    Ascendis Pharma (Princeton, NJ)
    Medical Director Do you want to be part of building a fully integrated biopharmaceutical company together with a team of highly skilled colleagues who are ... the Endocrine Medical Sciences team for the US business, the Medical Director handles deliverables and activities associated with management and implementation of… more
    Ascendis Pharma (12/10/24)
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  • Director , Human Factors

    Merck (Rahway, NJ)
    **Job Description** The Director , Human Factors plays a pivotal role in combination product development (both design and process), commercialization and lifecycle ... in our company's portfolio and pipeline including acquisition products. This Director position will interact extensively with all subject-matter experts within the… more
    Merck (11/21/24)
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  • Director of Quality Assurance & Safety

    Compass Group, North America (Raritan, NJ)
    …at interesting locations? Come grow your career with Eurest. Job Summary The Director of Quality Assurance & Safety is responsible for developing and maintaining all ... the flow. + Manages Allergen Preventive Controls Program ensuring accurate allergen labeling on finished food products and prevention of allergen cross contact. +… more
    Compass Group, North America (11/02/24)
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  • Director , Clinical Development

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    ** Director , Clinical Development** **Join a Legacy of Innovation 125 Years and Counting!** Daiichi Sankyo Group is dedicated to the creation and supply of innovative ... to Health Authority) + Participant and voting member in the labeling development process in the Labeling Working Team (LWT), in collaboration with the CDL +… more
    Daiichi Sankyo Inc. (12/20/24)
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  • Quality Assurance Director

    Compass Group, North America (New York, NY)
    …but the start of a career where you can flourish. Job Summary The Director of Quality Assurance will lead the development and execution of comprehensive QA programs ... requirements. + Oversee the Allergen Preventive Controls Program, ensuring accurate allergen labeling and prevention of cross-contact in line with Kirkland & Ellis… more
    Compass Group, North America (10/24/24)
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  • Associate Director , WW Medical…

    Bristol Myers Squibb (Princeton, NJ)
    …lives. Read more: careers.bms.com/working-with-us . **Position: Associate Director , WW Medical Neuropsychiatry Strategy, Schizophrenia** **Location: Princeton ... Pike or Madison, NJ** The Associate Director of Medical Strategy, Schizophrenia will partner with key medical team to support development, implement, and execute… more
    Bristol Myers Squibb (12/29/24)
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  • Associate Director , US Medical Promotional…

    Bristol Myers Squibb (Princeton, NJ)
    …lives. Read more: careers.bms.com/working-with-us . **Position:** Associate Director , Medical Promotional Review Scientist, Neuropsychiatry **Location:** Princeton ... Pike, NJ or Madison, NJ The Associate Director , Medical Promotional Review Scientist plays a critical role in the Medical Strategy team. As a member of this team,… more
    Bristol Myers Squibb (10/03/24)
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  • Senior Director , WW Medical…

    Bristol Myers Squibb (Princeton, NJ)
    …their personal lives. Read more: careers.bms.com/working-with-us . **Position: Senior Director , WW Medical Neuropsychiatry Strategy** **Location: Princeton Pike or ... provide medical affairs planning and support for other Neuropsychiatry indications. The Senior Director will lead a Medical Strategy team and report directly to the… more
    Bristol Myers Squibb (11/17/24)
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  • Sr. Director , PV Medical Surveillance

    Taiho Oncology (Princeton, NJ)
    Sr. Director , PV Medical Surveillance Princeton, NJ, USA Req #378 Monday, July 15, 2024 Looking for a chance to make a meaningful difference in the oncology space? ... Proposition: Embark on a transformative journey with Taiho Oncology as a Sr. Director , PV Medical Surveillance . At the forefront of pharmacovigilance innovation, we… more
    Taiho Oncology (10/14/24)
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  • Associate Director , Regulatory Affairs…

    Gilead Sciences, Inc. (Parsippany, NJ)
    …strategic and operational regulatory guidance on new concepts, campaigns, and product labeling for the assigned brands. You may manage complex interactions related ... RA Ad/Promo at Regulatory Project Team meetings. + Represents RA Ad/Promo at labeling meetings and provides strategic regulatory guidance. + Mentors RA Ad/Promo and… more
    Gilead Sciences, Inc. (11/16/24)
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  • Associate Director , Regulatory Affairs (In…

    Bristol Myers Squibb (Princeton, NJ)
    …with HA deadlines. + Contribute in the developing of target labeling . **Degree / Experience Requirements** + Bachelor's degree required; advanced scientific ... degree preferred (Masters, PhD, PharmD, BSN, etc.) with 5 years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience in successfully leading teams; ability to broadly represent the… more
    Bristol Myers Squibb (12/25/24)
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  • Supervisor, Quality Assurance

    Amneal Pharmaceuticals (Piscataway, NJ)
    …schedules and coordinates daily priorities for incoming raw materials and labeling components, in-process testing, finished product sampling, in-process labeling ... incoming raw material, in-process material, finished product and in-process packaging/ labeling operations sampling and inspection activities. + Trains, supervises… more
    Amneal Pharmaceuticals (12/05/24)
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  • Data Entry Specialist

    New York Edge (Staten Island, NY)
    …program. The Data Specialist will play a critical role in assisting the Program Director and New York Edge in running reports and tracking data which details the ... timely and accurate manner + Entering the schedule and labeling activities into required databases + Set up class...all required systems + Assist the After School Program Director to enhance programming through the use of Data… more
    New York Edge (12/24/24)
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