Copy Review, Sr Manager
Johnson & JohnsonAbout the role
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. Learn more at jnj.com
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.
Job Function:
Legal & ComplianceJob Sub Function:
Enterprise ComplianceJob Category:
People LeaderAll Job Posting Locations:
Raritan, New Jersey, United States of America, Raynham, Massachusetts, United States of America, West Chester, Pennsylvania, United States of AmericaJob Description:
DePuy Synthes is recruiting for a(n) Sr. Manager, Copy Review, located in West Chester, PA or in Raynham, MA or Raritan, NJ.
Job Overview
The Sr. Manager, Copy Review plays a critical leadership role in ensuring that all educational and promotional materials meet the highest standards of clarity, accuracy, and compliance. This role is central to how DePuy Synthes communicates scientific and product information to healthcare professionals, directly supporting safe and effective product use. You will collaborate across Commercial, Medical Affairs, Legal, and Regulatory teams to enable high-quality, compliant content that advances education and strengthens customer engagement.
Key Responsibilities:
• Lead the end-to-end copy review process for educational and commercial materials, ensuring accuracy, consistency, and compliance
• Review and approve content including training materials, educational programs, digital assets, and promotional communications
• Partner with Marketing, Medical Affairs, Legal, and Regulatory stakeholders to align messaging and ensure efficient approval cycles
• Provide subject matter expertise on claims, substantiation, and appropriate use of scientific and clinical data
• Establish and optimize processes, workflows, and best practices for copy review and content approval
• Ensure all materials align with internal policies, regulatory requirements, and industry standards
• Support innovation in content delivery, including digital education formats and tools
• Monitor timelines, workflows, and key performance metrics to improve review efficiency and effectiveness
• Mentor and guide team members to build capabilities in content quality, compliance, and review standards
• Contribute to a customer-focused approach through high-quality, clear, and impactful communications
Qualifications
Education:
• Bachelor’s degree required (e.g., Communications, Marketing, Life Sciences, Healthcare, or related field)
• Advanced degree (MBA, MS, MPH, or similar) preferred
Experience and Skills:
Required:
• Typically 8+ years of relevant experience in copy review, medical communications, regulatory review, or related function
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