• Quality & Regulatory Affairs Specialist

    Robert Half Finance & Accounting (Morristown, NJ)
    …in ensuring compliance with quality and regulatory standards within the pharmaceutical industry. Based in Basking Ridge, New Jersey, this position offers an ... The opportunity to work in a growing, innovative environment within the pharmaceutical industry. detail oriented growth and development in a compliance -focused… more
    Robert Half Finance & Accounting (08/09/25)
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  • Program Manager I, Quality Compliance

    Integra LifeSciences (Princeton, NJ)
    …material remediation experience. + Experience in implementing remediation programs, and working with compliance frameworks such as FDA , ISO 13485, and EU MDR is ... required + Strong analytical skills, exceptional writing and interpersonal relationship skills or a combination of relevant work experience and education is required. + Demonstrated organizational, management and communication skills is required. + Proven… more
    Integra LifeSciences (06/06/25)
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  • Senior/Patient Advocacy & Medical Society…

    United Therapeutics (Trenton, NJ)
    …are as follows:** Who We Are We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit ... a brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the availability of transplantable organs.… more
    United Therapeutics (08/23/25)
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  • Director, Regulatory Advertising & Promotion

    Sumitomo Pharma (Trenton, NJ)
    Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... relevant external advertising & promotional regulations or codes of practice (eg, FDA regulations, PhRMA guidelines, etc.) and are consistent with company guiding… more
    Sumitomo Pharma (07/08/25)
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  • Associate Director, Global Regulatory Affairs…

    Sanofi Group (Morristown, NJ)
    …and marketed products impacting potential US product promotion. Liaises with the FDA Office of Prescription Drug Promotion (OPDP) and Advertising and Promotion ... promotion, disease-state, market access, and press materials. Submits materials on form FDA 2253 when applicable. + Provides US RA AdPromo strategic guidance and… more
    Sanofi Group (08/12/25)
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  • Associate Director, Commercial Regulatory Affairs-…

    Bristol Myers Squibb (Princeton, NJ)
    …Ensure full regulatory compliance of all promotions with approved labeling and /or FDA guidances + Ensure regulatory compliance with sub part e and 2253 ... BMS guiding principles, PhRMA guidelines, FTC guidelines, and applicable FDA regulations and guidances. **Responsibilities include:** + Provides regulatory advice,… more
    Bristol Myers Squibb (08/25/25)
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  • Director US Labeling & Registration

    Bayer (NJ)
    …and accurate implementation of new and revised labeling in accordance with FDA requirements and provides regulatory expertise and guidance for labeling operations ... and analyzes and evaluates requests for new or revised labeling initiated by FDA or Bayer HealthCare Pharmaceuticals and manages action required to implement; +… more
    Bayer (08/07/25)
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  • Director of Monitoring, Ethics and Business…

    Sanofi Group (Morristown, NJ)
    …including email monitoring, live monitoring activities, and other projects in compliance with pharmaceutical industry regulations and company policies. As ... Excel and PowerPoint + Knowledge of key regulatory framework relevant to pharmaceutical email communications (eg, HIPAA, GDPR, FDA regulations, PhRMA Code)… more
    Sanofi Group (08/01/25)
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  • Executive Director of R&D Global Quality (Remote)

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …Skills: **Qualifications** + Bachelor's degree and 15+ years of experience in a FDA regulated pharmaceutical and/or medical device industry environment + Strong ... procedures to ensure that the business units quality management and compliance program are effective and efficient in identifying, detecting, and correcting… more
    Otsuka America Pharmaceutical Inc. (08/14/25)
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  • Senior Manager EQ Small Molecules

    J&J Family of Companies (Titusville, NJ)
    …of pharmaceutical products that meet or exceed safety, regulatory compliance , and product standards. **Key Responsibilities:** + Provide quality leadership and ... PA, Athens, GA, or Tampa, FL. At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working...+ A minimum of 8 years working in a FDA regulated environment. + Experience with quality support of… more
    J&J Family of Companies (08/29/25)
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