About the Role
Associate Medical Director, Medical & Scientific Affairs
Job Function: Patient Health & Regulatory Affairs
Location:
El Segundo, CA, US, 90245
Work Flexibility: Hybrid
Pay Range: $229,400 - $310,200
Job ID: 4840
Apply with account
Apply now
Location: El Segundo, CA | Goleta, CA | Stafford, TX | Auburn, Charlton, Franklin, MA
Up to 30% Travel
Why you will love this role:
Advance Surgical Innovation Through Clinical Insight.
At KARL STORZ, we are dedicated to improving patient outcomes through cutting-edge surgical innovation. As Associate Medical Director, Medical & Scientific Affairs (MSA), you will play a key role in connecting clinical practice with product innovation, providing scientific, clinical, and strategic expertise to support the safe and effective use of our medical technologies.
What you will be doing:
Serve as a clinical and scientific expert in general surgery, video and imaging platforms, and operating room integration products.
Partner cross-functionally with R&D, Regulatory Affairs, Quality, Legal, and Commercial teams to ensure clinical accuracy and sound medical decision-making throughout the product lifecycle.
Lead and support medical safety initiatives, including post-market surveillance, product recalls, and risk assessments to safeguard patient care.
Engage with Key Opinion Leaders (KOLs), facilitate advisory boards, and lead scientific and educational programs to advance product knowledge and adoption.
Collaborate with Clinical Affairs to assess and communicate clinical evidence, literature, and research insights that guide strategic decisions.
Provide medical input for product development, regulatory submissions, and educational content for healthcare professionals.
Represent KARL STORZ in external scientific forums and peer-to-peer clinical discussions while maintaining the highest standards of compliance and professionalism
What You Bring:
MD or DO degree required.
8+ years of surgical experience, including residency training (general surgery or closely related specialty preferred).
Strong foundation in medical device technology, clinical evaluation, and patient safety principles.
Demonstrated ability to communicate complex scientific concepts to diverse internal and external audiences.
Excellent leadership, collaboration, and organizational skills; able to thrive in dynamic, cross-functional settings.
Experience engaging with KOLs, advisory boards, or scientific education programs preferred.
Tech Stack
clinical medicineregulatory affairsmedical devicespost-market surveillanceproduct developmentrisk assessment