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
.
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 AnnualIf 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.
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.
BD seeks a driven Molecular Sales Specialist to join their team in Sparks, MD, promoting cutting-edge medical solutions to healthcare institutions.
Become part of BD, a renowned medical technology company, as a Distribution Associate responsible for warehousing and material distribution tasks.
Seeking a skilled Senior Specialist in Regulatory Affairs to join our dynamic team at a leading global health care innovator in De Soto, KS.
Join Lonza as a Regulatory Affairs Specialist, a fully remote role pivotal in regulatory compliance and innovation across life sciences.
Lead labeling strategies at a global biopharmaceutical company as a Senior Manager in Regulatory Affairs.
CorDx is looking for a Regulatory Affairs Manager to oversee regulatory documentation for medical device products, ensuring compliance and timely approvals.
Insmed is looking for a skilled Regulatory Affairs Manager experienced in project management to enhance global submission processes.
Lead the regulatory affairs advertising and promotion team for a biopharmaceutical leader in a remote capacity.
We are seeking a detail-oriented Regulatory Affairs Specialist to join our team and help navigate compliance in the dietary supplement industry.
Lead CMC regulatory strategies at AbbVie as a Senior Manager in a dynamic hybrid work environment in Irvine, CA.
Subscribe to Rise newsletter