Regulatory Affairs Specialist

Globus-Medical; Lower Providence Township (PA); Sur place; USD 70 000 - 100 000; Plein temps

Résumé du poste

Globus Medical seeks a Regulatory Affairs professional to perform thorough regulatory assessments for proposed product changes and support line extensions. You will review literature and marketing collateral to ensure compliance with US and international regulations, and collaborate with multiple departments to align plans and regulatory decisions.

The role requires 2+ years in medical devices, a Bachelor’s degree (or equivalent with Master’s), and a solid understanding of pre-market submission

Qualifications

• Bachelor’s degree required; or 1 year and a Master’s degree; or equivalent work experience.
• 2+ years of related experience in the medical device industry.
• Solid understanding of regulatory terminology and submission types.
• Able to evaluate regulatory impact of proposed product and process changes.

Responsabilités

• Performs regulatory assessment for proposed product changes, including supplier request changes.
• Demonstrates global regulatory expertise for change assessments with local regulations.
• Collaborates with departments to review plans and regulatory decisions for products or line extensions.
• Reviews product literature and marketing collateral to ensure regulatory compliance.

Connaissances

Regulatory knowledge

Pre-market submissions

Project planning

Multi-tasking

Deadline management

Communication

Formation

Bachelor’s degree

Master’s degree

Description du poste

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:Performs a thorough regulatory assessment for proposed changes to current products and provides Regulatory support for line extensions and supplier change requests, ensuring compliance with local and regional registration requirements. Conducts an in-depth review of product literature and marketing collateral for all products, with an emphasis on Class II devices, to ensure Regulatory compliance. Monitors and improves tracking and control systems. Keeps abreast of regulatory procedures and changes.Essential Functions :Performs a through regulatory assessment for proposed product changes, including supplier request changes and documents all related activates to remain in complianceDemonstrates global regulatory expertise for change assessments with local regulationsCollaborates with various departments to review the required plans, procedures and regulatory decisions for existing products or line extensionsConducts review of product literature and other marketing collateral (presentations, advertisements, social media posts, etc.) to ensure Regulatory complianceReviews technical publications, articles, and abstracts to stay abreast of regulatory and technical developments in the industryAdheres 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 this roleRepresents 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 partiesReasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.Qualifications :Typically requires a minimum of 2 years of related experience with a Bachelor’s degree; or 1 year and a Master’s degree; or equivalent work experienceTwo+ years of related experience in the medical device industryUnderstanding of regulatory requirements throughout the product lifecycleSolid understanding of regulatory terminology, pre-market submission types, and requirementsAble to evaluate regulatory impact of proposed product and process changesCapable multi-tasking skills with the ability to project plan and meet deadlinesResult driven with a sense of responsibility, urgency and ability to perform under pressurePhysical 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 crawlRequired to regularly lift and/or move up to 10 pounds, and occasionally lift and/or move up to 25 poundsRequired to possess specific visual abilities, including close vision, distance vision, color vision, peripheral vision, depth perception and capacity to adjust focusOur 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 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 accountable to one another and support each other. Together, we make each other stronger.Driven : We pursue our mission with energy and passion. We are nimble, results-oriented and decisive. We overcome obstacles that arise in our quest to deliver solutions that will improve the lives of our customers and patients.Equal Employment Opportunity :Globus Medical is an equal opportunity employer. All applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, age, disability, marital status, pregnancy, national origin or citizenship. We are committed to a diverse workforce. We value all employees’ talents and support an environment that is inclusive and respectful.Other Duties :Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.