Sr Regulatory Affairs Specialist

Globus Medical; King of Prussia (Montgomery County); On-site; USD 158,000 - 225,000; Full time

Job summary

An established industry player is seeking a Senior Regulatory Affairs Specialist to ensure compliance and enhance product strategies. This role involves coordinating regulatory submissions, collaborating with various departments, and staying updated on regulatory changes. The ideal candidate will have extensive experience in the medical device industry and a strong understanding of regulatory requirements. Join a dynamic team dedicated to improving patient care through innovative solutions and make a significant impact in the field of regulatory affairs.

Qualifications

• 5+ years experience in regulatory affairs within medical devices.
• Understanding of regulatory requirements throughout product lifecycle.
• Ability to evaluate regulatory impact of product changes.

Responsibilities

• Coordinates regulatory submissions ensuring compliance with regulations.
• Collaborates with departments for regulatory decisions on products.
• Monitors regulatory procedures and recommends strategies for approvals.

Skills

Regulatory Strategy

Regulatory Compliance

Product Lifecycle Knowledge

Multi-tasking Skills

Communication Skills

Analytical Skills

Education

Bachelor's Degree

Master's Degree

PhD

Job description

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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

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.

Essential Functions

• Determines the appropriate regulatory strategy for new products and documents all related activates 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
• Performs other duties as assigned 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
  
  

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

Qualifications

• 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
  
  

Physical Demands

The physical demands listed here are representative of those that must be met by and 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 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.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Legal

• Industries

  Medical Equipment Manufacturing

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