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Senior Specialist, Regulatory Affairs - Hybrid

Job Description SummaryAs 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 DescriptionWe are the makers of possibleBD 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 AnnualFor 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/careersBecton, 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.#CLOLIRequired SkillsOptional Skills.Primary Work LocationUSA CA - San Diego TC Bldg C&DAdditional LocationsWork ShiftAt 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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$121100K
$199800K

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

Join the BD team as a Senior Specialist in Regulatory Affairs and be part of something truly impactful! Located in Temecula, CA, this hybrid role allows you to engage with a global leader in medical technology while enjoying the flexibility of working from home. You’ll be at the forefront of supporting our MMS Dispensing products, which include medical and non-medical devices, along with essential software and accessories. In this position, you will play a vital role in new product development and ensure compliance with regulatory requirements. Your expertise will help navigate the complexities of FDA Medical Device Regulations and EU-MDR standards, making a real difference in the healthcare field. Not only will you be collaborating across various functional teams, but you will also have the chance to influence processes that foster customer satisfaction and regulatory adherence. If you have at least five years of experience in Regulatory Affairs, a strong educational background in a relevant field, and the desire to drive innovation, then this is the perfect opportunity for you to grow within a supportive environment that values your unique contributions. Become a maker of possible with BD as we advance the world of health together!

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

As a Senior Specialist in Regulatory Affairs at BD, you will be responsible for supporting the compliance of MMS Dispensing products with regulatory standards. This includes working on new product development, sustaining existing products, and managing end-of-life regulatory activities. You'll ensure that regulations such as the FDA Medical Device Regulations and EU-MDR are adhered to while collaborating with cross-functional teams to create and maintain technical files and registration documentation.

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What qualifications do I need to apply for the Senior Specialist, Regulatory Affairs position at BD?

To qualify for the Senior Specialist position in Regulatory Affairs at BD, candidates should possess a minimum of a 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. Additionally, a RAPS RAC certification is advantageous, along with a minimum of five years of relevant experience in Regulatory Affairs for medical devices.

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

At BD, career growth is highly prioritized. As a Senior Specialist in Regulatory Affairs, you will find a culture that values learning, collaboration, and development. The company offers robust training opportunities, mentorship programs, and a supportive team environment to ensure you can reach your professional goals and explore pathways for advancement within the organization.

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What is the salary range for the Senior Specialist, Regulatory Affairs position at BD?

The salary range for the Senior Specialist, Regulatory Affairs role at BD typically falls between $121,100.00 and $199,800.00 USD annually. This range may vary depending on several factors, including experience, education, skills, and the specific work location, ensuring competitive compensation tailored to individual qualifications.

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What skills are important for success as a Senior Specialist in Regulatory Affairs at BD?

Success in the Senior Specialist, Regulatory Affairs role at BD demands strong interpersonal, communication, and analytical skills. You should be adept at managing regulatory compliance across multiple projects, effectively prioritize tasks, and partner with cross-functional teams. Additionally, a solid understanding of global regulatory requirements, regulations, and standards related to medical devices is essential.

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Common Interview Questions for Senior Specialist, Regulatory Affairs - Hybrid
Can you describe your experience with FDA Medical Device Regulations?

When answering this question, emphasize your familiarity with FDA regulations, including any specific projects where you ensured compliance. Discuss any challenges you faced and how you overcame them, showcasing your problem-solving abilities and understanding of regulatory processes.

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How do you stay updated on the latest regulatory changes in the healthcare industry?

Illustrate your proactive approach to staying informed by mentioning relevant websites, journals, or industry conferences you follow. Highlight how you apply this knowledge in your current or past roles to demonstrate your commitment to continuous learning in the field of Regulatory Affairs.

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What strategies do you use for the creation and maintenance of technical files?

Discuss your organizational skills and attention to detail when creating technical files. Mention any methodologies or frameworks you follow, and share experiences where your strategic planning led to improved documentation processes or successful audits.

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Can you provide an example of a regulatory compliance issue you resolved?

Be ready to share a specific situation where you identified a compliance issue, how you assessed its impact, the steps you took to resolve it, and the outcome. Focus on your analytical skills and your ability to collaborate with others to find solutions.

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Describe your experience working cross-functionally with other teams.

Highlight your collaboration skills by providing examples of projects where you worked closely with departments like engineering, marketing, or quality assurance. Emphasize how you facilitated communication and teamwork to meet regulatory objectives.

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What is your approach to managing multiple projects with tight deadlines?

Explain your prioritization techniques, such as using project management tools or setting clear deadlines. Sharing a specific example where you successfully managed multiple tasks will strengthen your answer, demonstrating your effectiveness in high-pressure environments.

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What role do you think continuous improvement plays in Regulatory Affairs?

Articulate your understanding of continuous improvement principles and how they apply to Regulatory Affairs. Provide examples of initiatives you have undertaken to enhance processes or compliance that led to measurable improvements in efficiency or effectiveness.

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How do you ensure compliance with both domestic and international regulations?

Discuss your knowledge of and experience with both local and global regulatory requirements, emphasizing how you integrate this knowledge into your daily work to ensure compliance across jurisdictions.

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What process do you follow for preparing registration documentation?

Explain your systematic approach to preparing registration documents, including gathering information, collaborating with stakeholders, and ensuring all regulatory guidelines are met before submission.

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Why are you interested in working as a Senior Specialist in Regulatory Affairs at BD?

Craft a response that connects your professional background with BD's commitment to advancing health. Discuss your passion for regulatory affairs and how you envision contributing to BD’s goals while realizing your career aspirations within the company.

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Our Purpose: Advancing the world of health.

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Full-time, hybrid
DATE POSTED
December 17, 2024

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