[Hiring] Associate Medical Director @SOLVENTUM

Role Description

Associate Medical Director

At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers’ toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue.

The Impact You’ll Make in this Role:

• Provide medical insights for product development, risk assessments, and customer interactions.
• Oversee the design, execution, and analysis of clinical studies to support product approvals and post-market surveillance.
• Medical monitoring during clinical trials by reviewing safety data, assessing adverse events, and ensuring participant safety throughout the study.
• Provide medical expertise in complaint management.
• Develop and maintain relationships with key opinion leaders and industry experts to gather insights.
• Collaborate closely with R&D, Quality Assurance, Regulatory Affairs, and Marketing teams to align clinical objectives with business goals.
• Ensure compliance with all relevant regulatory requirements and guidelines.
• Contribute to the training of medical and non-medical personnel.
• Provide medical input for the development of marketing and educational materials.
• Support the development and execution of medical education and scientific evidence strategies.

Qualifications

• MD or equivalent medical degree AND a minimum of 5 years of clinical experience.
• Experience in a medical affairs role within the medical device industry.
• General, working knowledge of statistical principles, Good Clinical Practice concepts, and other regulations and standard practices governing clinical research, including medical monitoring.
• Lead cross-functional teams and manage complex projects.
• Deliver clear, accurate written and verbal communications when presenting complex information to stakeholders.
• Experience applying established processes/procedures to resolve work-related issues.
• Manage shifting priorities and complete work effectively in a fast‑paced environment.

Requirements

• Familiarity with medical device regulations.
• Advanced postgraduate qualifications in a relevant field like medicine, Management, etc.
• Active registration.
• Proficiency in additional languages is an advantage.

Benefits

• Competitive pay and benefits.
• Medical, Dental & Vision.
• Health Savings Accounts.
• Health Care & Dependent Care Flexible Spending Accounts.
• Disability Benefits.
• Life Insurance.
• Voluntary Benefits.
• Paid Absences.
• Retirement Benefits.