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.
Responsibilities
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.
Our generous benefits including but not limited to:
• Competitive salary
• Comprehensive benefits package including retirement savings plan, insurance (health, dental, vision) and more!
• Have a happier, healthier work life with less stress and more time for hobbies and interests by taking advantage of flexible paid time off and paid holidays!
• Relocation assistance may be available
Key responsibilities:
Review and approve labels, labeling, and promotional materials to ensure regulatory compliance.
Work closely and collaboratively with Marketing and project teams to develop, review, and substantiate product claims.
Review and evaluate protocols, reports, and journal articles to ensure collection of appropriate data to support promotional materials.
Drive the collection of regulatory intelligence for projects related to US and OUS labeling remediation.
Effectively communicate regulatory strategies to stakeholders.
Problem solve and escalate regulatory and compliance issues to senior management, as necessary.
Keep business partners informed of the status of regulatory owned tasks.
Perform gap analysis to support labeling projects and remediation activities.
Assist in drafting standard operating procedures, work instructions, and policies to maintain compliance with applicable regulations and standards.
Remain current on standards and regulations affecting advertising, promotion, and labeling and communicate the impact cross-functionally.
Perform other duties and assignments as required.
Professional Skills & Key Competencies
Excellent verbal and written communication skills.
Demonstrated ability to analyze, interpret, and review scientific, technical, and regulatory literature and documents while effectively communicating information to peers and management while working independently with minimum supervision.
Excellent attention to details.
Flexible and adaptable to fulfill business priorities.
Computer literacy (SAP, Microsoft Word / Excel / PowerPoint).
Manages time efficiently.
Knowledge of global Regulatory Affairs requirements.
Strong organizational skills
Ability to represent Regulatory Affairs in multiple environments (i.e., Marketing, R&D, etc.) and work with all levels of management.
Identify and communicate risks and mitigations associated with regulatory strategies to cross-functional collaborators.
Qualifications:
Bachelor’s degree in Life Sciences or Engineering.
Advanced degree (e.g. MS, Life Sciences) preferred
Minimum of five (5) years of Regulatory Affairs experience in the medical device and/or pharmaceutical industry preferred.
Strong prioritizing, interpersonal, communication, and analytical skills, and the ability to multi-task disparate projects
Knowledge of global Regulatory Affairs requirements, regulations, and standards
Desired/Additional Skills & Knowledge:
Familiarity and background with advertising, promotion, and labeling in the medical device industry.
Certifications
RAPS RAC preferred.
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.
Required Skills
Optional Skills
.
Primary Work Location
USA CA - San Diego TC Bldg C&DAdditional Locations
USA NC - Durham - Roche DriveWork 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 AnnualSuccess 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.