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Professional Education Manager (King of Prussia)

Maxx Orthopedics Inc. - King of Prussia, PA

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Job Description

About Maxx Orthopedics Maxx Orthopedics is a global orthopedic implant company focused on innovative, high-performance orthopedic solutions with an emphasis on large joints. We partner with surgeons worldwide to improve patient outcomes through advanced implant design and hands-on clinical education. Position Overview The Professional Education Manager will lead the design and execution of surgeon education programs that drive clinical adoption of Maxx Orthopedics systems. This role combines strategic program development with hands-on management of domestic and international training events, including responsibility for surgeon travel and logistics. Key Responsibilities Develop, plan and manage professional education initiatives such as cadaver labs, workshops, national & regional symposia, and digital training for orthopedic surgeons. Coordinate faculty engagement, speaker agreements, and honoraria for such activities in alignment with Maxx Orthopedics standards and industry compliance. Manage travel, accommodations, and logistics for surgeons and faculty attending such U.S. and international training programs. Ensure all activities meet compliance requirements (AdvaMed, Sunshine Act, GDPR, and local regulations). Design effective training programs that reduce the learning curve and facilitates the smooth adoption of newer technology the company introduces. Partner with Sales, Marketing, and Clinical Affairs to align education strategy with business goals. Monitor budgets, measure program outcomes, and report on effectiveness. Build relationships with key opinion leaders (KOLs) and training centers to strengthen Maxx Orthopedics US presence. Qualifications Bachelors degree required; advanced degree or healthcare background preferred. 5+ years of experience in professional/medical education, clinical training, or healthcare event management. Excellent verbal and written communication skills. Previous experience (2-3 years) in the management and coordination of clinical trials or regulatory submissions is essential. In executing the responsibilities of this position, intermittent, scheduled domestic and international travel will be required (30% total). Knowledge of orthopedic surgery, implants, or medical devices strongly preferred. Strong understanding of industry compliance standards. Excellent organizational, communication, and project management skills. PHYSICAL DEMANDS N (Not Applicable) Activity is not applicable to this position. O (Occasionally) Position requires this activity up to 33% of the time (0 - 2.5+ hrs/day) F (Frequently) Position requires this activity from 33% - 66% of the time (2.5 - 5.5+ hrs/day) C (Constantly) Position requires this activity more than 66% of the time (5.5+ hrs/day) Physical Demands Stand O Walk O Sit C Manually Manipulate O Grasp N Reach Outward N Reach Above Shoulder N Speak C Climb N Crawl N Squat or Kneel N Bend N Lift/Carry 10 lbs or less O 11-20 lbs N 21-50 lbs N 51-100 lbs N Over 100 lbs N Push/Pull 12 lbs or less O 13-25 lbs N 26-40 lbs N 41-100 lbs N Other Physical Requirements Vision (Near) WORK ENVIRONMENT Typical Office The success of our organization relies on the kind of creative thinking that can only result from a diverse team of individuals. The company is proud to be an Equal Employment Opportunity employer. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. EOE .

Created: 2025-09-29

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