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Senior Specialist, Regulatory Affairs - Hybrid

Job Description Summary

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

At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.

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

.

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

$124,700.00 - $205,800.00 USD Annual

Average salary estimate

$160450 / YEARLY (est.)
min
max
$121100K
$199800K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

What You Should Know About Senior Specialist, Regulatory Affairs - Hybrid, bdx

Are you ready to take your career to the next level with BD as a Senior Specialist in Regulatory Affairs? Located in sunny San Diego, California, this hybrid role is perfect for individuals looking to make a significant impact in the world of medical technology. At BD, we pride ourselves on being one of the largest global medical technology companies, with a mission to advance the world of health. Your primary responsibilities will include ensuring compliance with FDA and EU-MDR regulations, tackling regulatory and compliance issues, and driving continuous improvement in processes. You'll also monitor and interpret regulatory requirements, contribute to the creation of Technical Files, and support product labeling review. If you have a minimum of five years of experience in Regulatory Affairs within medical devices, a bachelor’s degree in a relevant field, and strong analytical skills, we want to hear from you! With us, you’ll enjoy a dynamic environment that fosters collaboration, creativity, and innovation. Work alongside cross-functional teams to address regulatory challenges and help ensure our products meet the highest standards. At BD, we believe in rewarding our associates fairly and competitively, and we’re committed to your growth and development. If you’re passionate about making a difference in healthcare and are ready to reinvent the future of health with us, this could be the perfect opportunity for you. Join us at BD, where your contributions matter, and discover a culture that supports your journey to become your best self.

Frequently Asked Questions (FAQs) for Senior Specialist, Regulatory Affairs - Hybrid Role at bdx
What are the key responsibilities of a Senior Specialist in Regulatory Affairs at BD?

As a Senior Specialist in Regulatory Affairs at BD, you'll play a crucial role in ensuring compliance with FDA and international regulations, particularly for medical devices. Your responsibilities will include monitoring regulatory changes, preparing and auditing registration documentation, and supporting the creation of Technical Files. You’ll also collaborate with cross-functional teams to identify regulatory challenges, drive continuous improvement in processes, and ensure adherence to Quality Management System (QMS) requirements.

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What qualifications are needed to become a Senior Specialist in Regulatory Affairs at BD?

To qualify for the Senior Specialist position in Regulatory Affairs at BD, you need a minimum bachelor’s degree in Regulatory Affairs, Quality Assurance, engineering, or a related scientific discipline. An advanced degree, such as a Master’s in Life Sciences, is preferred, along with RAPS RAC certification. Candidates should have at least five years of experience in Regulatory Affairs/Compliance in the medical device industry, along with strong communication and analytical skills.

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What is the work environment like for a Senior Specialist in Regulatory Affairs at BD?

At BD, the work environment for a Senior Specialist in Regulatory Affairs is collaborative and dynamic. The role is hybrid, allowing for a combination of in-office and remote work, supporting creativity and effective problem-solving. BD emphasizes teamwork, with opportunities to learn and grow alongside passionate colleagues. You’ll be part of a culture that prioritizes personal development and recognizes the value of each individual's contributions.

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How does BD support career growth for Senior Specialists in Regulatory Affairs?

BD is committed to investing in its associates' personal and professional growth. The company offers a robust development program, competitive compensation, and a variety of recognition opportunities that align with performance. As a Senior Specialist in Regulatory Affairs, you’ll have access to training and mentorship resources to help you enhance your skills and advance your career within the organization.

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What is the salary range for a Senior Specialist in Regulatory Affairs at BD in San Diego?

The salary range for a Senior Specialist in Regulatory Affairs at BD in San Diego varies depending on experience and qualifications, typically falling between $121,100.00 and $199,800.00 annually. Factors such as location, education, and skills contribute to the actual salary offered to successful candidates, ensuring competitive compensation within the medical technology industry.

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Common Interview Questions for Senior Specialist, Regulatory Affairs - Hybrid
Can you describe your experience with FDA and EU-MDR regulations?

When answering this question, provide specific examples of your work with FDA and EU-MDR regulations. Discuss any projects where you ensured compliance with these regulations, the challenges you faced, and how you addressed them. Highlight your analytical skills and how they have contributed to successful regulatory submissions.

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How do you stay updated on changes in regulatory requirements?

To effectively answer this question, share your strategies for keeping informed about regulatory changes. This may include following industry publications, participating in webinars, joining professional organizations, or networking with others in the Regulatory Affairs field. Emphasize your proactive approach to staying ahead of regulations that impact your work.

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Describe a time you faced a regulatory compliance issue. How did you resolve it?

When discussing a specific compliance issue, outline the situation, actions you took, and the successful outcome. Use the STAR method (Situation, Task, Action, Result) to structure your response, demonstrating your problem-solving skills and ability to navigate complex regulatory environments.

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What strategies do you use to manage multiple projects simultaneously?

In response to this question, highlight your organizational skills and time management techniques. Explain how you prioritize tasks, delegate responsibilities when necessary, and ensure that each project aligns with regulatory timelines. Providing examples from your previous experience can showcase your effectiveness in multitasking.

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How do you approach cross-functional collaboration in your role?

Discuss your experience working with various teams, emphasizing your interpersonal communication skills. Provide examples of successful collaborations, how you foster teamwork, and the importance of relationships in achieving regulatory goals. Balance your answers by discussing challenges faced in collaboration and how you navigated them.

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What role does data analysis play in your regulatory affairs work?

In your answer, illustrate the significance of data analysis in regulatory affairs. Discuss how you use data to inform decisions, analyze compliance outcomes, or support submission documentation. Providing relevant experiences can help underline the importance of analytical skills in this position.

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What processes do you follow to create Technical Files?

When responding, outline the steps you take to ensure Technical Files are comprehensive and compliant with regulatory standards. This may include gathering documentation, confirming product specifications, and collaborating with different teams to facilitate the process. Emphasize attention to detail and the importance of thoroughness in your work.

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Can you provide an example of a successful regulatory submission you worked on?

To effectively answer this question, describe the submission process, your specific contributions, and the outcome. Highlight any challenges you faced and how you overcame them, showcasing your expertise and understanding of regulatory frameworks.

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How do you handle feedback from regulatory agencies?

Discuss your approach to receiving and acting on feedback from regulatory agencies. Emphasize your adaptability and willingness to adjust strategies based on feedback, showcasing your commitment to continuous improvement and regulatory compliance.

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What motivates you to work in Regulatory Affairs?

When addressing this question, share your passion for regulatory compliance and its vital role in healthcare. Talk about your commitment to protecting public health and medical innovations, explaining how these motivations drive your work within Regulatory Affairs.

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EMPLOYMENT TYPE
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DATE POSTED
April 23, 2025

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