Job ID R-501046 Date posted December 5, 2024

Be part of something bigger at BD. Here, you’ll help us maintain our high standards from a regulatory perspective at all levels, with a keen focus on submissions. It requires acute attention to detail, excellent communication skills and a passion to keep learning and updating your knowledge, which we’ll help you do with regular learning opportunities. Here, you’ll use your in-depth knowledge of FDA, Canadian and ISO/MDD regulations and requirements surrounding medical devices to ultimately achieve a singular goal: advancing the world of health™. At BD, you can make a true difference of one.

  • Job Type:
    Full-Time
  • Job Level:
    Entry to Senior
  • Travel:
    Varies
  • Salary:
    Competitive
  • Glassdoor Reviews and Company Rating

Responsibilities

Job Description Summary

As Sr. Specialist of Regulatory Affairs you will be responsible for supporting MMS Dispensing products consisting of Medical Devices and Non-Medical Devices along with associated Software and Accessories on a global basis from a Regulatory Affairs standpoint. Support will consist of new product development, sustaining, and end of life activities. Candidates must be able to work in our San Diego, CA office 4 days per week.

Job Description

We are the makers of possible 

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 us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to 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. 

Primary Responsibilities:

  • Support regulatory effort to comply with new and existing regulations (e.g., FDA Medical Device Regulations, EU-MDR)

  • Problem solve and escalate regulatory and compliance issues to senior management as necessary

  • Drive continuous improvement in internal processes and customer satisfaction

  • Support the monitoring and interpreting of current and new regulatory requirements and international standards for U.S. and RoW

  • Support that QMS requirements are followed and executed consistently from RA perspective

  • Support efforts for Technical File creation, remediation, and collaboration with cross-functional teams for required content

  • Support regulatory impact assessments for change controls and other RA/QA items from a review and approve level

  • Assist in preparing, auditing, editing, and publishing registration documentation as needed

  • Support business export control (BEC) listing of product for release globally per RA requirements

  • Support the review and approval of product labeling, promotional, and advertising materials as needed.

About You:

    • Minimum bachelor’s degree in RA, QA, engineering, or other science-related discipline

    • Advanced degree (e.g. MS, Life Sciences) preferred

    • RAPS RAC certification preferred

    • Minimum of 5 years of strong Regulatory Affairs/Compliance experience in medical devices

    • Knowledge of global Regulatory Affairs requirements, regulations, and standards

    • Strong prioritizing, interpersonal, communication, and analytical skills, and the ability to multi-task disparate projects

    • Excellent interpersonal, communication, and analytical skills and able to  partner with cross-functional colleagues to identify regulatory innovation

    Salary ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates’ progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary offered to a successful candidate is based on experience, education, skills, and actual work location. Salary ranges may vary for Field-based and Remote roles.

    121,100.00 - 199,800.00 USD Annual

    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.  

    To learn more about BD visit https://bd.com/careers

    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. 

    #CLOLI

    Required Skills

    Optional Skills

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    Primary Work Location

    USA CA - San Diego TC Bldg C&D

    Additional Locations

    Work Shift

    At BD, we are strongly committed to investing in our associates—their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You.

    Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates’ progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary or hourly rate offered to a successful candidate is based on experience, education, skills, and any step rate pay system of the actual work location, as applicable to the role or position. Salary or hourly pay ranges may vary for Field-based and Remote roles.

    Salary Range Information

    $121,100.00 - $199,800.00 USD Annual
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    Success Profile

    What makes a successful Regulatory Affairs Professional at BD? Check out the top traits we’re looking for and see if you have the right mix.

    • Analytical
    • Collaborative
    • Communicator
    • Persuasive
    • Problem-solver
    • Skilled presenter

    Advancing the world of health™

    BD is one of the largest global medical technology companies in the world and is advancing the world of health™ by improving medical discovery, diagnostics and the delivery of care. BD helps customers enhance outcomes, lower costs, increase efficiencies, improve safety and expand access to health care.

    At BD, we are committed to global inclusion and diversity. Increased inclusion and diversity drives innovation, allows us to better understand patient and customer needs, and ultimately makes BD the best possible place for all associates to thrive.


    Brian Carney
    Staff Regulatory Affairs Specialist

    I love working with high powered leaders on a day to day basis who are respectful to my opinion and who I was never exposed to in my past job.


    Robin Cassell
    Global Regulatory Operations Labeling Specialist

    I have been trusted in my ability to lead exciting and challenging projects with excellent upper management support. This in-turn has allowed me to grow and expand my regulatory knowledge that I believe will lay as a foundation to build my Regulatory career on.


    Nikita A Mahendra Kumar
    Senior Regulatory Affairs Specialist

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