Field Clinical Engineer

What You’ll Do: Provide on-site support during implantation and follow-up procedures involving Class III medical devices. Troubleshoot technical issues during procedures and provide immediate, clinically sound recommendations. Act as the subject matter expert on device function and clinical applications. Educate physicians, nurses, and allied health professionals on device functionality, therapy benefits, and procedural workflows. Conduct in‑service trainings, workshops, and ongoing clinical education for new and existing users. Support collection of clinical data and user feedback to assist with regulatory submissions, product development, and continuous improvement efforts. Document field interactions in compliance with quality and regulatory standards. Collaborate with R&D, Regulatory, Safety, and Commercial teams to relay device deficiencies and clinical insights. Assist with investigational device trials, product evaluations, and site initiation visits. Ensure all activities are performed in accordance with company policies, local regulations, and international standards (e.g., FDA, ISO 13485, MDR).

Who You Are: You possess a deep understanding of clinical environments and have the ability to navigate complex procedures with ease. Your communication skills are exceptional, allowing you to educate and engage healthcare professionals effectively. You are adaptable, capable of prioritizing urgent site needs while maintaining strong internal stakeholder relationships. Your analytical mindset helps you provide insightful feedback and solutions, contributing to product advancements. You thrive in dynamic settings and are passionate about improving patient outcomes through innovative medical technologies.

Required Skills: Bachelor’s degree in Biomedical Engineering, Nursing, Life Sciences, or a related field. At least 7 years of experience in a clinical or field support role for implantable medical devices. Demonstrated experience providing field support for intrathecal device use during clinical procedures. Experience working in compliance with clinical trial regulations, SOPs, and study protocols.

Preferred Skills: Advanced degree (MS, PhD) or clinical credentials.

Job Level: Management

Additional Information: The base compensation range for this role is: $131,000.00-$175,250.00. Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity. Regular employees are eligible to receive both short term and long term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.

Benefits: Medical, Dental, Vision, & Life insurances Fitness & Wellness programs including a fitness reimbursement Short- and Long-Term Disability insurance A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31) Up to 12 company paid holidays + 3 paid days off for Personal Significance 80 hours of sick time per calendar year Paid Maternity and Parental Leave benefit 401(k) program participation with company matched contributions Employee stock purchase plan Tuition reimbursement of up to $10,000 per calendar year Employee Resource Groups participation Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid‑sized biotechnology company, we provide the stability and resources of a well‑established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life‑changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about Biogen. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States. As Biogen recently acquired Apellis, you can find additional open jobs on our Apellis website here.