Sr Medical Affairs Specialist

About the role

B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety. B. Braun Medical is headquartered in Bethlehem, Pa., and is part of the B. Braun Group of Companies in the U.S., which includes B. Braun Interventional Systems, Aesculap® and CAPS®. Globally, the B. Braun Group of Companies employs more than 64,000 employees in 64 countries. Guided by its Sharing Expertise® philosophy, B. Braun continuously exchanges knowledge with customers, partners and clinicians to address the critical issues of improving care and lowering costs.

The Sr. Medical Affairs Specialist serves as a clinical subject matter expert, providing advanced medical, scientific, and product support to internal stakeholders and external customers. This role is responsible for evaluating and documenting product incident reports involving patient injuries, delivering accurate clinical guidance, responding to complex product inquiries, and developing evidence-based medical communications. The specialist partners closely with Product Quality Engineering, Marketing, Research & Development, and Product Development teams to provide clinical expertise that supports patient safety, product lifecycle management, and business strategy. Working with a high degree of independence, the Sr. Medical Affairs Specialist contributes to medical affairs strategy, customer education, and cross-functional initiatives while ensuring compliance with regulatory requirements, company policies, and standard operating procedures. The role also participates in an on-call rotation to address urgent clinical and technical inquiries and may represent the organization through scientific presentations and customer engagements.

Responsibilities

• Provide clinical input and assistance to PQE during product incident report (PIR) intake and documentation per SOP.
• Document product incident reports (PIR) involving patient injury based on SOP. Record relevant information concerning product complaints