Sr. Director, Strategic Collaboration Orthopedics

Johnson & Johnson Johnson & Johnson · Pharma · Zuchwil, Switzerland

This role is a Sr. Director of Strategic Collaboration within Quality & Compliance at Johnson & Johnson's DePuy Synthes, focusing on deploying enterprise-wide quality and compliance strategies. It requires leading cross-functional alignment, translating strategy into deployable programs, and ensuring regulatory readiness and operational excellence in a highly regulated healthcare environment. The role involves people leadership and driving continuous improvement in collaboration and deployment effectiveness.

What you'd actually do

  1. Lead strategic collaboration initiatives across Quality & Compliance to ensure alignment and effective execution of enterprise priorities.
  2. Translate quality and compliance strategy into deployable programs, governance models, and execution frameworks.
  3. Partner with senior leaders across Quality, Regulatory Affairs, Manufacturing, Commercial, and Supply Chain to drive cross‑functional alignment.
  4. Establish and oversee deployment plans, milestones, and performance metrics for strategic initiatives.
  5. Identify execution risks, interdependencies, and gaps and drive mitigation actions.

Skills

Required

  • Bachelor’s degree in Engineering, Quality, Life Sciences, Regulatory Affairs, Business, or a related discipline
  • 12-14 years of progressive experience in Quality, Compliance, Regulatory, or related roles within a regulated industry
  • Demonstrated senior leadership experience driving enterprise-level strategy and cross-functional initiatives
  • Strong understanding of quality systems and regulatory requirements in global organizations
  • Proven ability to influence and align senior stakeholders across complex, matrixed environments
  • Experience leading large‑scale deployment or transformation initiatives
  • Excellent strategic thinking, communication, and change‑management skills
  • English required

Nice to have

  • Master’s degree or MBA
  • Experience in medical devices, healthcare, or other highly regulated industries
  • Experience working in global or multi‑regional organizations
  • Exposure to audit, inspection, or regulatory interaction at the enterprise level
  • Demonstrated success driving collaboration and execution across diverse stakeholder groups
  • Quality or Regulatory certifications (e.g., ASQ, RAC)
  • additional European languages preferred

What the JD emphasized

  • senior leadership
  • enterprise-level strategy
  • cross-functional initiatives
  • quality systems
  • regulatory requirements
  • senior stakeholders
  • complex, matrixed environments
  • large-scale deployment
  • transformation initiatives
  • regulated industry