Bachelor's degree in health or science-related field, or equivalent; Engineering degree is a plus
Minimum of 2-5 years' experience in Regulatory Affairs in the medical device industry, , preferably within orthopedic medical devices;
Experience in medical device development and registration of products
Demonstrated knowledge of US regulatory submissions; Pre-Sub, and 510(k); working knowledge of IDE and PMA submissions a plus
Experience assessing regulatory impact of product/process changes
Experience reviewing labeling, promotional literature, etc.
Excellent communication and listening skills
Proficient with Microsoft Office, including Word, Excel, PowerPoint and Teams
Strong time management skills, demonstrated ability to work on multiple projects, priorities simultaneously
Able to work independently as well as within a team
Physical Demands :
The physical demands listed here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
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 visons abilities, including: close vision, distance vision, color vision, peripheral vision, depth perception and capacity to adjust focus
Our Values :
Our Life Moves Us philosophy is built on four values: Passionate About Innovation, Customer Focused, Teamwork, and Driven.
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
Benefits
Health insuranceVision insurance
Additional Information
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.
Position Summary:
The Regulatory Affairs Specialist assists with drafting, submitting and gaining clearance for 510(k) submissions, and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products. This position entails development of FDA submissions, requires working knowledge of products under review and of relevant regulations and guidance documents. This individual must be enthusiastic, positive, even-tempered and effective in building working relationships with internal teams while following FDA 21 CFR regulations.
Essential Functions:
Partners with Product Development and management to prepare and review 510(k) submissions
Prepares final 510(k) submissions and obtaining required management approvals
Submits 510(k) documents and responding to the FDA in a timely manner
Assists in the completion of IDE and PMA submissions for IDE clinical trials
Helps to prepare PMA packages, including non-clinical, manufacturing, and clinical sections
Works with personnel in various functional areas to obtain timely submissions to FDA
Obtains and reviews clinical study data with Clinical Data Manager and other Clinical Affairs personnel, as needed for IDE and PMA reporting
Reviews Document Change Orders for Regulatory compliance, including drawings and labeling changes
Performs routine maintenance of approved PMAs, including coordination and preparation of PMA supplements, Annual Reports
Trains new staff on relevant Regulatory processes as necessary
Determines Regulatory Pathway for new/changed products under departmental guidelines
Reviews and approve Regulatory Pathway Forms and supporting documentation
Reviews and approves Note-to-File documentation for minor changes to 510(k) cleared products or systems
Understands the company's products, surgical techniques and the use of implant and instrument systems
Develops relevant Regulatory SOPs as necessary
Adheres to the letter and spirit of the company Code of Conduct, the AdvaMed Code, MedTech 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 uphold the highest standards of ethical business practices and socially responsible conduct in all interactions with other employees, customers, suppliers, and other third parties of Globus
Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.
Globusmedical · Audubon, PA