Executive Director, Regulatory Affairs - United States - Bridgewater, NJ

Only for registered members United States - Bridgewater, NJ

1 week ago

Default job background

Job summary

Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference.


Lorem ipsum dolor sit amet
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.

Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.

Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
Get full access

Access all high-level positions and get the job of your dreams.



Similar jobs

  • Work in company

    Regulatory Affairs

    Only for registered members

    +The candidate would be expected to have a good understanding of the Health Authority query process and the submission translation process to help us support new releases of our systems. · +Product Manager for regulatory submission process · Health Authority query process · ...

    Raritan

    5 days ago

  • Work in company

    Regulatory Affairs Intern

    Only for registered members

    The Cosette 2026 Summer Internship Program gives students an opportunity for experiential learning in a corporate environment.This role offers a unique opportunity to understand how regulatory strategy directly enables product development, · approval,and post-marketing success. · ...

    Bridgewater Internship

    1 month ago

  • Work in company

    Regulatory Affairs Intern

    Only for registered members

    The Regulatory Affairs intern will gain hands-on exposure to compiling Annual Reports and Periodic Adverse Drug Experience Reports (PADERs) that are filed to the FDA. · This role offers a unique opportunity to understand how regulatory strategy directly enables product developmen ...

    Bridgewater

    1 month ago

  • Work in company

    Regulatory Affairs Manager

    Only for registered members

    + Job summary: Regulatory Affairs Manager is responsible for contributing to and implementing regulatory strategies and tactics for the Company. · + Responsibilities:Act as a primary contact for regulatory affairs on cross-functional product development and post-marketing teams. ...

    Bridgewater

    1 month ago

  • Work in company

    Regulatory Affairs Intern

    Only for registered members

    The Cosette · 2026 Summer Internship Program gives students an opportunity for experiential learning in a corporate environment.This is an 11-week, full-time program for rising junior and senior undergraduate students at an accredited college or university. · The summer internsh ...

    Bridgewater, NJ

    1 month ago

  • Work in company

    Regulatory Affairs Intern

    Only for registered members

    The Regulatory Affairs intern will gain hands-on exposure to compiling Annual Reports and Periodic Adverse Drug Experience Reports (PADERs) that are filed to the FDA. · They will also learn how to create labels and patient information for Branded and Generic products. · This role ...

    Bridgewater, NJ

    1 month ago

  • Work in company

    Regulatory Affairs BA

    Only for registered members

    Regulatory Affairs BA with 10+ years experience in Global Regulatory affairs, CMC submissions. Knowledge on Insights and regulatory affairs. · ...

    Raritan

    1 month ago

  • Work in company

    Team Lead – Regulatory Affairs

    Only for registered members

    The company Net2Source is an employer-of-choice for over 1000 consultants across the globe. They recruit top-notch talent for over 40 Fortune and Government clients coast-to-coast across the U.S. · ...

    Bridgewater

    2 weeks ago

  • Work in company

    Delivery lead—Regulatory affairs

    Only for registered members

    The job description states that Net2Source, Inc. is one of the fastest growing IT Consulting company across USA. The role of Delivery Lead - Regulatory Affairs involves being the first point of contact for client regional lead and for hub related queries, working in close collabo ...

    Bridgewater

    2 weeks ago

  • Work in company

    Team Lead-Regulatory Affairs

    Only for registered members

    Necesita experiencia de más de cinco años en publicación de presentaciones electrónicas y mantenimiento rutinario de IND. · Tener buena comprensión del ciclo de vida del medicamento. · ...

    Bridgewater

    2 weeks ago

  • Work in company

    Regulatory Affairs Specialist-V

    Only for registered members

    This individual will be part of the Global Regulatory Affairs team. · This role assists with planning, writing, compilation,and editing of periodic regulatory reports. · ...

    Bridgewater, NJ

    1 week ago

  • Work in company

    Team Lead – Regulatory Affairs

    Only for registered members

    This is a Team Lead – Regulatory Affairs job in Bridgewater. It involves developing and mentoring associates by providing expertise in all submission types applicable to their region of responsibility. · ...

    Bridgewater

    2 weeks ago

  • Work in company

    Executive Director, Regulatory Affairs

    Only for registered members

    We are seeking an experienced Regulatory Affairs Director to lead our regulatory strategy and ensure compliance with global regulations. The ideal candidate will have a strong understanding of the drug development process and excellent organizational skills. · Formulate and imple ...

    Bridgewater

    2 weeks ago

  • Work in company

    Jr. Publisher – Regulatory Affairs

    Only for registered members

    Jr. Publisher – Regulatory Affairs · (Bridgewater) · ...

    Bridgewater

    2 weeks ago

  • Work in company

    Team Lead – Regulatory Affairs

    Only for registered members

    +h2>Job Summary · Develops and mentors associates by providing expertise in all clinical electronic publishing submission types applicable to their region of responsibility. Leads team of publishers , manages people. · +Diploma/ Bachelor degree in Pharmacy, Life-Science · Minimu ...

    Bridgewater

    2 weeks ago

  • Work in company

    Sr. Publisher – Regulatory Affairs

    Only for registered members

    Sr. Publisher – Regulatory Affairs at Net2Source, Inc. · Responsible for global regulatory submission / dossier publisher day-to-day activities and deliverables. · ...

    Bridgewater

    2 weeks ago

  • Work in company

    Regulatory Affairs Specialist III

    Only for registered members

    This position will provide strategic support to the company's regulatory affairs efforts by providing expertise in submissions and compliance with FDA regulations. · ...

    Bridgewater, NJ

    1 week ago

  • Work in company

    Jr. Publisher – Regulatory Affairs

    Only for registered members

    Preparar, rastrear, compilar y publicar suministros regulatorios para asignados. · Diploma/ Bachelor degree in Pharmacy. · ...

    Bridgewater

    2 weeks ago

  • Work in company

    Regulatory Affairs Operations

    Only for registered members

    The contractor will provide Regulatory Affairs Operations support focused on BLA compilation and quality control activities. · Bachelor's degree in a life science pharmacy regulatory science or related discipline. · 2+ years' experience in regulatory submissions compilation or do ...

    Warren Township $50 - $75 (USD) Freelance

    3 weeks ago

  • Work in company

    Regulatory Affairs Operations

    Only for registered members

    + Job summary + · The contractor will provide Regulatory Affairs Operations support focused on BLA compilation and quality control (QC) activities. · + ResponsibilitiesSupport assembly and maintenance of BLA submission modules (including CMC, nonclinical, and clinical sections) · ...

    Warren, NJ Freelance

    3 weeks ago