Sr Regulatory Affairs Specialist

At Globus Medical, we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the needs of these patients, and the surgeons and healthcare providers who treat them. We embrace a culture of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions.

Our solutions improve the techniques and outcomes of surgery so patients can resume their lives as quickly as possible.

Coordinates and prepares document packages for regulatory submissions for new and mature products, ensuring compliance with local and regional registration requirements. Compiles all materials required in submissions, license renewal and annual registrations. Recommends changes for labeling, manufacturing, marketing and clinical protocol for regulatory compliance. Monitors and improves tracking and control systems. Keeps abreast of regulatory procedures and changes. Recommends strategies for earliest possible approvals of clinical trials applications.

• Determines the appropriate regulatory strategy for new products and documents all related activities to remain in compliance
• Demonstrates global regulatory expertise in product submissions and evaluates changes with local regulations
• Collaborates with various departments to review the required plans, procedures and regulatory decisions for new or existing products
• Reviews regulatory requirements from other departments for new product designs or changes to existing designs
• Reviews technical publications, articles, and abstracts to stay abreast of regulatory and technical developments in the industry
• Prepares and maintains regulatory pre‑market submissions and other pre‑market filings to assist in acquiring appropriate commercial distribution clearances
• Supports product import by providing applicable regulatory documentation and certificates
• Adheres to the letter and spirit of the company Code of Conduct, the Adva Med Code, Med Tech Code, and all other company policies
• Ensures compliance with applicable governmental laws, rules, and regulations, both in the United States and internationally, by completing introductory and annual training and maintaining knowledge of compliance as it applies to your role
• Represents the company in a professional manner and upholds the highest standards of ethical business practices and socially responsible conduct in all interactions with other employees, customers, suppliers, and other third parties

Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.

• Typically requires a minimum of 5 years of related experience with a Bachelor’s degree; or 3 years and a Master’s degree; or a PhD without experience; or equivalent work experience
• 5+ years of related experience in the medical device industry
• Understanding of regulatory requirements throughout the product lifecycle
• Solid understanding of regulatory terminology, pre‑market submission types, and requirements
• Able to evaluate regulatory impact of proposed product and process changes
• Capable multi‑tasking skills with the ability to project plan and meet deadlines
• Result driven with a sense of responsibility, urgency and ability to perform under pressure

• Required to sit; climb or balance; and stoop, kneel, crouch or crawl
• Required to regularly lift and/or move up to 10 pounds, and occasionally lift and/or move up to 25 pounds
• Required to possess specific vision abilities, including close vision, distance vision, color vision, peripheral vision, depth perception and capacity to adjust focus

• Passionate about Innovation:
  Improving patient care by delivering advanced technology to our customers is at the core of what we do. We are passionate in our role in improving the lives of patients by continuously developing better solutions.
• Customer Focused:
  We listen to our customers’ needs and respond with a sense of urgency.
• Teamwork:
  Working together, anything is possible. We value every person on our team and treat each other with respect. We are…