Head Regulatory Affairs Joints in Leeds

Head Regulatory Affairs Joints in Leeds

Leeds Full-Time 75600 - 92400 £ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Lead regulatory strategies for innovative medical devices and ensure timely product launches.
  • Company: Join Johnson & Johnson, a leader in healthcare innovation and inclusivity.
  • Benefits: Competitive salary, diverse work environment, and opportunities for professional growth.
  • Other info: Flexible locations across the globe with a focus on collaboration and innovation.
  • Why this job: Make a real impact on global healthcare with cutting-edge technologies and a passionate team.
  • Qualifications: 10+ years in regulatory affairs, preferably in medical devices, with strong leadership skills.

The predicted salary is between 75600 - 92400 £ per year.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative, and comprehensive orthopedic and neurological business in the world. DePuy Synthes Companies offer an unparalleled breadth and depth of products, services, and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, craniomaxillofacial, power tools and biomaterials. As the leading Orthopedic company, we are committed to a world where patients have access to care that is personalized and connected. Together with customers, we are shaping the future of healthcare with technically and clinically sophisticated innovations that bring value for the global healthcare system.

Purpose: DePuy Synthes, a member of Johnson & Johnson family of companies, is currently recruiting for a Sr. Director, Regulatory Affairs, Joints, Digital and Power tools. This individual may be based in Warsaw, Indiana; Raynham, MA; Palm Beach Gardens, FL; West Chester, PA; Leeds, UK; Cork, Ireland; or Zuchwil, Switzerland with a minimum of 25% travel to Warsaw, Indiana.

The Sr. Director, Regulatory Affairs is responsible for developing and implementing a strategic vision and operational plans for the Regulatory Affairs team to support the Platforms’ and Regulatory Affairs’ strategic objectives. This role will ensure timely regulatory clearances and registrations in support of key product launches required to support the Platforms’ global business plans with a focus on strategic markets. This role will also be a key contributor to the Joints, Digital and Power tools Leadership Teams, as well as the DePuy Synthes Regulatory Affairs Leadership Team. The role will report to the WW Vice President, Regulatory Affairs, DePuy Synthes.

Key Responsibilities:

  • Serve as a key leader on Joints, Digital and Power tools Leadership Teams, as well as the DePuy Synthes Regulatory Affairs Leadership Team.
  • Develop and implement a strategic vision and operational plans for the Regulatory Affairs team to support the Platforms’ and Regulatory Affairs’ strategic objectives.
  • Assure timely regulatory clearances and registrations in support of key product launches required to support the Platforms’ global business plans with a focus on strategic markets.
  • Lead the development and execution of strategies supporting the most expeditious regulatory pathways for introduction of VELYS technologies in targeted markets.
  • Develop and implement the overall regulatory strategy for digital technologies, including robotics, sensors, wearables, and apps, within the Joint Reconstruction Platforms’ overall business strategy.
  • Assess external innovation opportunities – both screening and technical due diligence.
  • Partner with R&D and other Platform leaders to develop and implement strategies for pipeline development.
  • Exercise highly sophisticated level of independent judgment and execution directly impacting the Platforms’ operational results.
  • Supervise the regulatory environment globally and provide assessments to Platform management of the impact of new and changing regulations on the Platforms.
  • Build an organization with the right talent and capabilities to implement regulatory support.
  • Encourage, empower and communicate vision to regulatory associates and peers.
  • Ensure aligned and coordinated contact and communication with global and regional/local regulatory agencies.
  • Lead, coordinate and balance resource allocation across multiple critical projects.
  • Ensure that company policies, procedures and practices are in compliance with appropriate regulatory requirements.
  • Provide progress updates to key business team members on a regular and as-needed basis.
  • Represent DePuy Synthes strategies in various internal and external forums.
  • Establish and ensure deployment of learning initiatives and training of Platform personnel on current and emerging regulatory and related requirements.

Required Qualifications / Requirements:

  • Minimum of a B.A./B.S. is required.
  • Minimum of 10 years relevant, medical devices regulatory affairs experience is required. Previous experience with orthopedic devices is highly preferred.
  • A minimum of 5 years of people management experience is required. Experience managing distributed, multi-national teams is preferred.
  • Senior leadership experience is required, including line management of multiple levels of reporting.
  • Proven success in partnering and influencing across a cross-functional environment is required.
  • Proven track record of formulating and implementing global regulatory strategies in support of strategic business objectives is required.
  • Previous experience with advanced digital technologies i.e. Data Science, Wearable Devices, Sensors, and/or Robotics is required.
  • The ability to demonstrate relations with key constituents to deliver tangible results and clinical insights is required.
  • Proven effective leadership and change management skills are required.
  • The ability to actively develop talent and culture to achieve results is required.

Preferred:

  • M.S., J.D., Ph.D. or M.D. is a plus.
  • Professional demeanor and service orientation; standout colleague.
  • Experience working with professional and trade associations is a plus.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state, or local law.

Head Regulatory Affairs Joints in Leeds employer: Johnson & Johnson MedTech

At Johnson & Johnson MedTech, we pride ourselves on being an exceptional employer that fosters a dynamic work culture focused on innovation and collaboration. Our North UK team offers a structured development plan, competitive compensation, and ample opportunities for personal and professional growth, making it an ideal environment for passionate individuals eager to make a meaningful impact in the healthcare sector.

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Contact Details:

Johnson & Johnson MedTech Recruitment Team

We think you need these skills to ace Head Regulatory Affairs Joints in Leeds

Regulatory Affairs
Strategic Vision Development
Operational Planning
Regulatory Clearances
Product Launch Support
Leadership Skills
Cross-Functional Collaboration