BD (Becton, Dickinson and Company) Regulatory Operations Labeling, Sr. Manager in Franklin Lakes, New Jersey

Job Description SummaryIn this newly created position reporting to the VP of Regulatory Operations, the Senior Manager of Global Labeling will play a lead role in building and refining BD's global labeling processes and capabilities, and provide strategic guidance in the development and maintenance of the regulatory content of global labeling, instructions for use (IFUs and eIFUs) etc., including leading cross-functional labeling team workstream for BD's EU Medical Device Regulations (MDR)/In-Vitro Diagnostics Regulations (IVDR) program.

Job Description

• Lead BD's Regulatory labeling function in Regulatory Affairs, and build new, scalable capability and processes to support BD's growth as a commercial organization.

• Provide strategic guidance to Core Labeling Teams regarding current and new labeling regulations, competitor labeling, and labeling trends.

• Collaborate with Global Regulatory Leads and R&D line the development of labeling strategies and target labeling, IFUs, etc., for new products as well as geo-expansion of products.

• Coordinate labeling activities with external alliance partners as required.

• Establish processes that ensure accurate records of the data sources supporting labeling claims, history of labeling negotiations and changes, and reasons for differences in labeling in the US, are captured.

• Coordinate with stakeholders (such as R&D, Supply Chain, Quality, Operations) regarding timing of labeling supplements, and communicate deadlines for implementation of the labeling changes.

• Monitor regulatory environment for new or revised legislation, regulations and guidance documents for health authorities related to product labeling, and assess and communicate impact to BD.

• Partner with Regulatory Affairs business Unit Leaders and Supply Chain to ensure submission-ready labeling components comply with regulatory requirements.

• Maintain any necessary electronic databases for product labeling.

• Develop or revise procedures as needed

• Maintains awareness of competitive activities. Monitors US and global regulatory environment by reviewing regulatory guidelines, untitled and warning letters to companies published by FDA, and by attendance of appropriate DIA and other industry/FDA meetings.

• Provide educational training for local regulatory staff, contractors and others regarding company policies and procedures where appropriate.

• Assist with additional regulatory projects as needed. Serves as part of the corporate Regulatory Operations team that drives the strategy for centralization of key functional support.

• Able to assess processes to recommend and drive to efficient future state processes including gaining buy in for key stakeholders

• Assess and provide recommendations of best practices between business units and drive to standardization of processes where possible.


  • Strong leadership and influence management skills and the ability to function effectively in large matrix organizations.

  • Excellent analytical and problem solving skills

  • Sound working knowledge of the Global regulatory environment

  • Strong coaching and mentoring skills

  • Ability to effectively communicate complex issues and programs to all levels of the organization.

  • Experience and knowledge of PC/database skills

  • Experience and knowledge of document management systems

  • Leadership:Proven ability to earn the trust of leaders within the organization, including senior leadersProven ability to mobilize, motivate and direct a matrix team towards a common vision and common set of objectivesProven ability to resolve conflict (striving for win-win outcomes)Proven ability to deliver tough messages in a professional mannerProven ability to act independently and to execute with limited information and ambiguity

Education and/or Experience:

  • Bachelor degree in science or health related discipline (Advanced degree PhD, MD, MS, PharmD preferred)

  • Detail-oriented with the ability to promptly assess documents for accuracy as well as consistency

  • Strong interpersonal skills with the ability to influence others in a positive and effective manner

  • Ability to work in a team environment

  • Working knowledge of Medical Device and IVD development and approval process and life cycle maintenance

  • Excellent communication skills; both oral and written

  • Prior experience in developing and maintaining medical device and IVD product labeling, managing or coordinating core labeling activities for first-time commercialization or product launch.

  • Minimum of 6 years of professional experience of relevant medical device with 3 years of relevant labeling experience. Broad knowledge of the med tech industry. Demonstrated ability to contribute to a continuous learning and process improvement environment.

Primary Work LocationUSA NJ - Franklin Lakes

Additional Locations

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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