Talent.com
Senior Director Regulatory Affairs, Dispensing

Senior Director Regulatory Affairs, Dispensing

Becton DickinsonSan Diego, CA, US
30+ days ago
Job type
  • Full-time
Job description

Sr. Director, Regulatory Affairs

BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of usfrom design and engineering to the manufacturing and marketing of our billions of MedTech products per yearto look at the impossible and find transformative solutions that turn dreams into possibilities.

We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us.

The Sr. Director, Regulatory Affairs is the ranking Regulatory Affairs leader for the Dispensing and Pharmacy Automation RA organization under the Medication Management Business Unit. This position is accountable for driving stakeholder engagement, partnering closely with Leadership Teams to further the International Dispensing and Pharmacy Automation Platform innovation agenda, building and maintaining effective relationships with regulators, including applicable Notified Bodies, and key market regulators.

This position provides expertise and leadership to business partners and executes regulatory strategies and objectives for product development programs and sustaining projects in alignment with business needs, drive timelines for global submission / clearance targets, including compliance, and effectively manage the RA team to ensure functional excellence.

Responsibilities :

  • Develops the regulatory strategic roadmap and provides regulatory leadership for programs in the domestic and international space
  • Provides strategic guidance to ensure alignment of regulatory strategies with business objectives and implementation of the strategic plans
  • Actively contribute to key strategic decisions impacting the development of global regulatory compliance policies, processes, and procedures
  • Establishes organization goals and objectives and integrates those into the team's responsibilities
  • Creates and defines regulatory pathways for new products; develops regulatory strategies and tactical plans for submissions regulatory bodies
  • Liaises with global RA lead(s), to ensure strategic alignment as needed
  • Identifies and communicates potential risks and mitigations associated with regulatory strategies to stakeholders
  • Directs the preparation of product information for product registrations
  • Incorporates Worldwide regulatory developments affecting the Business Group's Platforms and Programs and communicates emerging opportunities and concerns to stakeholders
  • Manages a staff of regulatory professionals responsible for product submission / registration activities
  • Assesses resource requirements based on business priorities and allocates personnel as required to meet these objectives
  • Develops direct reports required competencies, including, but not limited to, regulatory knowledge and ability to apply and communicate this knowledge
  • Conducts training on regulatory issues for staff and for business stakeholders (e.g., Clinical, R&D., Marketing)
  • In conjunction with RA business partners, provides input into the budget process for Regulatory Affairs
  • Represents the Platform in interactions / negotiations with global regulatory agencies and Notified Bodies; enables / empowers staff to interact and negotiate with regulators
  • Represents the Platform in external activities benefiting BD including trade associations, professional organizations, and standards development organizations
  • Ensure Regulatory resources are available to support inspections conducted by global regulators

Qualifications :

  • M.S. degree in a technical discipline (e.g., engineering, biology, chemistry, regulatory science). Advanced degree preferred (Ph.D, MBA)
  • Experience with Medical devices, pumping systems and / or software driven electromechanical devices required
  • Minimum ten (10) years of direct professional experience (Regulatory) in increasingly responsible positions in the medical device field and seven (7) years of management experience
  • Demonstrated ability to resolve problems and to make appropriate regulatory decisions under pressure
  • Experience in negotiating with regulatory agencies and Notified Bodies required
  • Demonstrated success in the preparation and completion (including negotiations) of regulatory submissions required
  • Demonstrated leadership skills
  • Demonstrated project management, negotiation, and communication (written and oral) skills
  • Demonstrated global perspective, customer focus, cross-functional collaboration and teamwork skills
  • Current and comprehensive knowledge of global regulations and quality systems are required
  • Strong project coordination, business acumen and negotiation abilities.
  • Proven management skills of multi-cultural, multi-national teams, leading and motivating all the Associates towards the shared goals achievement and the individual development
  • Travel up to 30%
  • For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and / or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.

    Why Join Us?

    A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable and learn and improve every day.

    To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place.

    Becton, Dickinson and Company is an Equal Opportunity / Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

    Required Skills

    Optional Skills

    Salary Range Information $199,600.00 - $359,300.00 USD Annual

    Create a job alert for this search

    Director Regulatory • San Diego, CA, US

    Related jobs
    • Promoted
    RayzeBio Director of Regulatory Affairs - Clinical / NonClinical

    RayzeBio Director of Regulatory Affairs - Clinical / NonClinical

    Bristol Myers SquibbSan Diego, CA, US
    Full-time
    We are seeking an experienced and innovative Director in Regulatory Affairs (clinical and nonclinical).This Global Regulatory Lead (GRL) position will report to the Head of Regulatory Affairs and w...Show moreLast updated: 22 days ago
    • Promoted
    Senior Regulatory Project Manager

    Senior Regulatory Project Manager

    Becton DickinsonSan Diego, CA, US
    Full-time
    Senior Regulatory Project Manager.The Senior Regulatory Project Manager is responsible for regulatory strategy development and execution of Companion Diagnostics (CDx) and IVD products.The Senior R...Show moreLast updated: 22 days ago
    • Promoted
    Global Regulatory Affairs Compliance and Planning, Sr. Manager

    Global Regulatory Affairs Compliance and Planning, Sr. Manager

    Kyowa KirinLa Jolla, CA, US
    Full-time
    Kyowa Kirin is a global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four areas of unmet need : oncology, nephrology, imm...Show moreLast updated: 30+ days ago
    • Promoted
    Sr. Regulatory Affairs Manager

    Sr. Regulatory Affairs Manager

    Katalyst Healthcares & Life SciencesSan Diego, CA, US
    Full-time
    Responsibilities : The Regulatory Manager provides regulatory strategy and development guidance for optimal conduct of clinical trials, regulatory agency meetings, orphan designations, pediatric pla...Show moreLast updated: 30+ days ago
    • Promoted
    Associate Director / Director, CMC Regulatory Affiars

    Associate Director / Director, CMC Regulatory Affiars

    Ionis BrandCarlsbad, CA, US
    Full-time
    Associate Director / Director, CMC Regulatory Affairs.Headquartered in Carlsbad, California, and with offices in Boston, Massachusetts, and Dublin, Ireland, Ionis has been at work for more than three...Show moreLast updated: 30+ days ago
    • Promoted
    Director- Research & Development Tax Credits (R&D)

    Director- Research & Development Tax Credits (R&D)

    EisnerAmperLa Jolla, CA, United States
    Full-time
    At EisnerAmper, we look for individuals who welcome new ideas, encourage innovation, and are eager to make an impact.Whether you're starting out in your career or taking your next step as a seasone...Show moreLast updated: 29 days ago
    • Promoted
    Senior Director, Nucleic Acid Therapy

    Senior Director, Nucleic Acid Therapy

    VertexSan Diego, CA, US
    Full-time
    Senior Director Of Nucleic Acid Therapy.Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious diseases.The compan...Show moreLast updated: 14 days ago
    • Promoted
    Director, Regulatory Affairs - Gene Therapy

    Director, Regulatory Affairs - Gene Therapy

    InsmedSan Diego, CA, US
    Full-time
    The Director, Regulatory Affairs will serve as the regulatory leader on cross-functional teams, where they will be responsible for guiding strategy, identifying risks, interpreting regulations and ...Show moreLast updated: 30+ days ago
    • Promoted
    • New!
    Senior Director of Accreditation, Regulatory and Contracts - Healthcare

    Senior Director of Accreditation, Regulatory and Contracts - Healthcare

    Mission HealthcareSan Diego, CA, US
    Full-time
    Senior Director Of Accreditation, Regulatory And Contracts - Healthcare.Mission Healthcare, located in seven states, is the largest home health and hospice company in the western United States.We h...Show moreLast updated: less than 1 hour ago
    • Promoted
    Manager, Regulatory Affairs - Hybrid - 134458

    Manager, Regulatory Affairs - Hybrid - 134458

    UC San Diego HealthSan Diego, CA, United States
    Full-time
    This position will remain open until a successful candidate has been identified.Eligible Special Selection clients should contact their Disability Counselor for assistance.This position will work a...Show moreLast updated: 30+ days ago
    • Promoted
    Director Quality Assurance Regulatory Affairs

    Director Quality Assurance Regulatory Affairs

    BioTalentCarlsbad, CA, United States
    Full-time
    Director of Quality & Regulatory Affairs – Medical Devices.Location : North San Diego | 💼 Full-time | 🏥 Medical Device Industry. We are seeking a Director of Quality & Regulatory Affairs to provide...Show moreLast updated: 2 days ago
    • Promoted
    Senior Director, Nanotechnology

    Senior Director, Nanotechnology

    Poseida TherapeuticsSan Diego, CA, United States
    Full-time
    The newly formed Genetic Medicine Technology group in gRED (Genentech Research and Early Development) is redefining the future of cell and gene therapies. Our proprietary non-viral gene delivery and...Show moreLast updated: 30+ days ago
    • Promoted
    Associate Director Regulatory Affairs

    Associate Director Regulatory Affairs

    AbbottSan Diego, CA, US
    Full-time
    Associate Director Regulatory Affairs.At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life.Career development with an...Show moreLast updated: 30+ days ago
    • Promoted
    Senior Director, Pharmaceutical Strategy and Development Leader

    Senior Director, Pharmaceutical Strategy and Development Leader

    Crinetics PharmaceuticalsSan Diego, CA, US
    Full-time
    Senior Director, Pharmaceutical Development Team Leader (PDTL).Crinetics is a pharmaceutical company based in San Diego, California that develops much-needed therapies for people with rare endocrin...Show moreLast updated: 30+ days ago
    • Promoted
    Regulatory Affairs Specialist II

    Regulatory Affairs Specialist II

    Katalyst Healthcares & Life SciencesSan Diego, CA, US
    Full-time
    Responsibilities : This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U. Europe, support of international product registrations ...Show moreLast updated: 30+ days ago
    • Promoted
    Associate Director Regulatory Affairs

    Associate Director Regulatory Affairs

    Abbott LaboratoriesSan Diego, CA, United States
    Full-time
    Abbott is a global healthcare leader that helps people live more fully at all stages of life.Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses an...Show moreLast updated: 30+ days ago
    • Promoted
    Sr Manager Regulatory Affairs

    Sr Manager Regulatory Affairs

    DexComSan Diego, CA, US
    Full-time
    Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM).Dexcom began as a small company with a big dream : To forever change how diabetes is managed.To...Show moreLast updated: 4 days ago
    • Promoted
    Senior Director, Clinical Trial Supplies

    Senior Director, Clinical Trial Supplies

    Crinetics PharmaceuticalsSan Diego, CA, US
    Full-time
    Senior Director, Clinical Trial Supplies.Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-rela...Show moreLast updated: 7 days ago
    • Promoted
    Manager, Regulatory Affairs - Hybrid - 134458

    Manager, Regulatory Affairs - Hybrid - 134458

    University of California San DiegoSan Diego, CA, United States
    Full-time
    CANCER CENTER / Clinical Trials Office.Days, 8 hrs / day, Monday-Friday.Manager, Regulatory Affairs - Hybrid.Extended Deadline : Tue 9 / 2 / 2025. UC San Diego values equity, diversity, and inclusion.If you ...Show moreLast updated: 30+ days ago
    • Promoted
    Regulatory Director- IVD and 510(k)

    Regulatory Director- IVD and 510(k)

    CorDxSan Diego, CA, US
    Full-time
    Director Of Regulatory Affairs.CorDx, a multi-national biotech organization focused on pushing the limits of innovation and supply in global health, delivers rapid testing and point-of-care medical...Show moreLast updated: 30+ days ago