Associate Director, Regulatory Affairs, Specimen Management Job at BD, Franklin Lakes, NJ

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  • BD
  • Franklin Lakes, NJ

Job Description

Associate Director, Regulatory Affairs, Specimen Management Join to apply for the Associate Director, Regulatory Affairs, Specimen Management role at BD Associate Director, Regulatory Affairs, Specimen Management 19 hours ago Be among the first 25 applicants Join to apply for the Associate Director, Regulatory Affairs, Specimen Management role at BD Get AI-powered advice on this job and more exclusive features. Job Description Summary The Associate Director, Regulatory Affairs, Specimen Management (SM) reports directly to the Vice President, Regulatory Affairs, Specimen Management. This position is responsible for regulatory activities and personnel supporting the Specimen Acquisition (SA) business growth and sustaining agenda. The role includes responsibilities for directing and evolving the regulatory strategy for the SA Platform, interacting with regulatory authorities and Notified Bodies to ensure SA’s growth and continued right to operate, supporting SA New Product Development and sustaining efforts, identifying and championing innovative regulatory approaches, collaborating within the RA function and cross-functionally to drive success, and leading and inspiring a team of regulatory affairs associates. This role will directly engage with both the SM RA Leadership Team and the SA Platform Leadership Team. Job Description Summary The Associate Director, Regulatory Affairs, Specimen Management (SM) reports directly to the Vice President, Regulatory Affairs, Specimen Management. This position is responsible for regulatory activities and personnel supporting the Specimen Acquisition (SA) business growth and sustaining agenda. The role includes responsibilities for directing and evolving the regulatory strategy for the SA Platform, interacting with regulatory authorities and Notified Bodies to ensure SA’s growth and continued right to operate, supporting SA New Product Development and sustaining efforts, identifying and championing innovative regulatory approaches, collaborating within the RA function and cross-functionally to drive success, and leading and inspiring a team of regulatory affairs associates. This role will directly engage with both the SM RA Leadership Team and the SA Platform Leadership Team. 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. BD’s Specimen Management Regulatory Affairs organization is the keystone of Specimen Management’s product registration efforts, connecting internal and external stakeholders to deliver safe, effective, and innovative diagnostic collection and care devices to patients and customers in alignment with business priorities and global regulations. About The Role In this role you will lead regulatory strategies and ensure compliance, driving growth and innovation in our team. Key Responsibilities Will Include Leading BD’s Specimen Management Regulatory Affairs team for the Specimen Acquisition Platform. Collaborating with SM business leaders and functions to drive initiatives and execution. Aligning regulatory strategies with business plans to foster growth, innovation, and profitability. Developing and implementing policies to ensure compliance with FDA, EU MDR, and international requirements. Acting as the primary contact for regulatory agencies, providing documentation, and ensuring comprehensive review. Leading regulatory audits and preparing regulatory records and documentation. Advocating favorable regulations for timely patient access to products. Driving SM RA strategies for New Product Development and sustaining efforts. Building strong regulatory capabilities and leadership within the team. About You You are a problem solver who excels in simplifying complex issues within broader business contexts, with a proven track record in regulatory submissions and negotiations. Your leadership encourages high-performing teams, embraces diverse perspectives, and uses innovative solutions to drive growth and compliance. Education And Experience Required At least 10 years of experience in the IVD/medical device field with growing responsibility. Minimum 3 years of management experience. Proven success in developing systems for regulatory submissions and acquiring timely approvals. Extensive knowledge of global regulatory strategies and experience with FDA Class I and II products. Significant experience with EU MDR or equivalent experience and Notified Body engagements. Demonstrated ability in regulatory advocacy, policy, and recruiting high-performance RA teams. Success in large, matrix-managed organizations, partnering with MA, QA, and R&D. Comprehensive knowledge of regulatory requirements in the U.S., EU, and other international markets. Click on Apply if this sounds like you! 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. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time. And through the organization’s investment in BD University, you will continually level up your tech skills and expertise. 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 Employer. 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. Required Skills Optional Skills Primary Work Location USA NJ - Franklin Lakes Additional Locations Work 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 $177,700.00 - $293,100.00 USD Annual Seniority level Seniority level Not Applicable Employment type Employment type Full-time Job function Job function Legal Industries Biotechnology Research, Medical Equipment Manufacturing, and Research Services Referrals increase your chances of interviewing at BD by 2x Sign in to set job alerts for “Associate Director Regulatory Affairs” roles. Regulatory Affairs Sr. Specialist (Hybrid Role - New York) New York, NY $100,000.00-$120,000.00 1 week ago Regulatory Affairs Manager - Medical Device New York, NY $110,000.00-$125,000.00 2 months ago Hawthorne, NY $107,500.00-$131,500.00 3 weeks ago Senior Regulatory Affairs Specialist - Urgent Need Jersey City, NJ $125,000.00-$135,000.00 3 days ago Legal, Regulatory, Compliance Project Management - Senior Consultant Secaucus, NJ $130,000.00-$140,000.00 1 month ago Associate Director, Global Regulatory Affairs – Global Labeling Strategy Morristown, NJ $147,000.00-$212,333.33 2 weeks ago Sr. Regulatory Affairs Specialist - Franklin Lakes, NJ Franklin Lakes, NJ $106,600.00-$175,900.00 3 days ago Franklin Lakes, NJ $177,700.00-$293,100.00 3 weeks ago Senior Regulatory Affairs Specialist, Mako and Enabling Technologies (Hybrid) Sr Regulatory Affairs Strategy Specialist Franklin Lakes, NJ $92,700.00-$152,900.00 2 weeks ago Regulatory Affairs Regional Associate Director, LACan East Hanover, NJ $132,300.00-$245,700.00 2 days ago New York, NY $150,000.00-$160,000.00 2 days ago Senior Manager, Regulatory Affairs, Mako and Enabling Technologies Regulatory Affairs & Consumer Product Consultant We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr BD

Job Tags

Hourly pay, Full time, Remote work, Shift work,

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