Sr. Regulatory Affairs Specialist

Becton Dickinson NA; Covington (GA); Hybrid; USD 110,000 - 140,000; Full time

Job summary

Becton Dickinson NA is seeking a Senior Regulatory Affairs Specialist to lead regulatory submissions (FDA 510(k), EU MDR) and maintain quality systems for U.S. and international markets. The role supports RA management and regulatory strategy across product lifecycles.

The position offers on-site work four days per week in Covington, GA, with remote Fridays, and requires 4+ years of medical device regulatory experience and strong documentation skills.

Qualifications

• Bachelor of Science in a scientific discipline, engineering or regulated field.
• Minimum 4 years of Regulatory Affairs experience in medical devices.
• Experience with product registration, regulatory compliance and quality system activities.

Responsibilities

• Regulatory support through the product life cycle on project teams, including strategy, change control, timelines and submission reviews.
• Prepare and revise STED/Technical Files for CE marking and interaction with Notified Bodies.
• Support post-market activities including remedial actions and labeling.
• Prepare/assist FDA 510(k) submissions and change assessments.
• Travel up to 15% as needed.

Skills

Regulatory strategy

FDA 510(k)

EU MDR

Technical writing

Cross-functional teamwork

Regulatory submissions

Project management

Communication skills

Education

BS in Science/Engineering

Tools

RAC certification

Job description

We are the people who give possibilities purposeBD 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.

Job Description

Urology and Critical Care (UCC) is an established and trusted partner in urinary healthcare, developing complete solutions which optimize the urine drainage process in the Acute Care Hospital setting. The Senior Regulatory Affairs Specialist is responsible for preparation of U.S and CE marking submissions/registration activities, along with supporting all other geographical regions registrations. In addition, this position will help support RA management. This role provides the flexibility to work on-site 4 days weekly in Covington, and remotely Friday on a weekly basis.

Key responsibilities

• Regulatory support through the product life cycle on product project teams (e.g., developing regulatory strategies, change control, timeline development, and reviewing submission related documents).
• Prepare &or revise STED technical files for CE marking activities and notified body interaction to support EU/MDR product maintenance, as required.
• Provide support and guidance for post market activities including remedial actions, labeling.
• Prepare and support 510(k) &/or change assessments, as required.
• Limited travel required - 15%.

Minimum Requirements

• Education: Bachelor of Science (BS) degree required, preferably in a scientific discipline, engineering, or other regulated field.
• Experience: Minimum 4 years of Regulatory Affairs experience within the medical device industry.
• Experience supporting product registration, regulatory compliance, and quality system activities for medical devices.
• Technical Knowledge: Working knowledge of U.S. FDA regulations, including 21 CFR Part 820, and European Medical Device Regulation (EU MDR).
• Experience with: U.S., EU, and international product registration activities.
• Medical device quality systems and regulatory compliance.
• Preparation and submission of FDA 510(k) premarket notifications.
• Development and maintenance of technical documentation, including STED/Technical Files.
• Interactions with regulatory authorities and/or EU Notified Bodies.

Core Competencies

• Demonstrated ability to support products throughout the product lifecycle, including product development, design changes, and post-market activities.
• Experience developing regulatory strategies, conducting change assessments, and managing regulatory deliverables and timelines.
• Strong technical writing skills with the ability to prepare clear, accurate, and compliant regulatory submissions.
• Ability to maintain confidentiality when handling regulatory, clinical, and business-sensitive documentation.
• Strong organizational and project management skills with the ability to prioritize multiple projects and meet deadlines.
• Self-motivated with the ability to work independently, exercise sound judgment, and take ownership of responsibilities.
• Effective written and verbal communication skills with demonstrated success working on cross-functional teams.

Work Arrangement

Ability to work on-site in Covington 4 days per week with remote work on Fridays

Travel

Willingness to travel up to 15% as needed

Preferred Qualifications

• Education: BS degree specifically in a Scientific Field (such as Biology, Chemistry, Biomedical Engineering)
• Certification: Regulatory Affairs Certification (RAC) from the Regulatory Affairs Professionals Society (RAPS)
• Product Knowledge: Familiarity with Class II medical devices, particularly in the urology or acute care hospital setting
• Advanced Skills: Experience leading regulatory activities on cross-functional product development teams.
• Ability to influence project teams and communicate regulatory risks and mitigation strategies.
• Strong analytical skills for evaluating technical data and determining regulatory impact.
• Excellent communication skills for interactions with regulatory authorities, Notified Bodies, auditors, and cross-functional stakeholders.

Work Culture

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.

Vaccination Requirement

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?

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 healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive. We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success. To learn more about BD visit https://bd.com/careers .Becton, Dickinson, and Company is an Equal Opportunity Employer.

Equal Opportunity Statement

We evaluate applicants without regard to 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, and other legally protected characteristics.

Contact / General Information

• Primary Work Location: USA GA - Covington BMD
• Additional Locations
• Work Shift: US BD 1st Shift 8am-430pm (United States of America)