Associate Director Regulatory Affairs (Hybrid) - Becton Dickinson Join to apply for the Associate Director Regulatory Affairs (Hybrid) - Becton Dickinson role at BD Associate Director Regulatory Affairs (Hybrid) - Becton Dickinson 3 days ago Be among the first 25 applicants Join to apply for the Associate Director Regulatory Affairs (Hybrid) - Becton Dickinson role at BD 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. 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. This role provides flexibility to work 4 days at our San Diego site and Friday remotely on a weekly basis. Summary Of Job Responsibilities The Associate Director of Regulatory Affairs will provide regulatory support for medical device systems within infusion technologies. The role includes but is not limited to the development and implementation of regulatory strategies for new product submissions, project management for regulatory affairs submissions, handling existing product registrations including variations and renewals, interacting with global internal stakeholders as well as external consultants/service providers in support of registration activities, developing and maintaining documentation for compliance programs such as labeling, promotional material review, and other regulatory requirements. Key Accountabilities Lead submission activities for various initiatives Work closely with cross-functional teams on submission strategy and documentation development for new product submissions Coordinate interactions between internal stakeholders and external service providers to ensure timely completion of submission milestones. Assist in the maintenance of departmental systems used to track projects and ongoing operational activities. Directly interface with regulators as needed. Perform additional tasks as required. Education Bachelor's degree in a scientific discipline: Engineering, Biology, etc. or equivalent. Advanced degree (Master's degree or higher) preferred. Regulatory Affairs Certification (RAC) preferred. Project Management Certification preferred. Experience Minimum 10 years of relevant work experience including experience within the Medical Device industry. Minimum of 5 years of experience in Regulatory Affairs working with complex medical device systems and software strongly preferred. Experience working with external service providers, consultants, and regulators required. Familiarity with Infusion Pump Systems preferred. Ability to travel up to 20% domestically and internationally may be required. Skills & Competencies Strong project management skills and organizational abilities. Excellent written and verbal communication skills. Proficiency in Microsoft Office Suite, especially Word, Excel, and PowerPoint. Proven ability to handle multiple priorities simultaneously while meeting deadlines. Demonstrated interpersonal skills necessary to optimally collaborate across departments and geographies. Proactive approach to problem solving with strong attention to detail. Team player who takes initiative. 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 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.
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