Regulatory Affairs Specialist 3

As a part of the global industrial organization Marmon Holdingswhich is backed by Berkshire Hathawayyoull be doing things that matter leading at every level and winning a better way. Were committed to making a positive impact on the world providing you with diverse learning and working opportunities and fostering a culture where everyones empowered to be their best.

Job Scope

The Regulatory Affairs Specialist 3 develops and executes regulatory strategy and integrates regulatory requirements throughout the product lifecycle. Relies on extensive experience and judgment to plan create develop and maintain materials needed for regulatory compliance. Uses technical knowledge to drive new product submissions listings and registration of medical devices. Trains and mentors lower-level specialists in regulatory activities.

Responsibilities

• Ensures all processes for the essential functions are documented in procedures.
• Performs internal departmental audits and supports audits by third parties e.g. BSI FDA and others as required.
• Initiates and maintains required establishment listings e.g. FDA and EU including renewal or changes.
• Develops company regulatory strategies and prioritization. Determines the best strategy to register new products in specific global markets.
• Determines appropriate product testing to support registration activities.
• Ensures content accuracy and regulatory compliance for submission to regulatory agencies e.g. 510(k) PMA MDR Technical Files/Design Dossiers global registration applications etc.
• Provides feedback / approval of compliant labeling e.g. IFUs marketing materials package labels etc.
• Manages and leads responses to Regulatory Agency for submission deficiencies.
• Maintains accurate international product registration including renewal or changes and certificates for foreign governments.
• Provides direction/guidance as needed to other Regulatory Specialists.

Qualifications

• 5 years of regulatory experience in medical device industry (equivalent industry/educational experience may be considered)
• Evidence of applied knowledge of applicable FDA ISO MDR requirements consensus standards and guidance documents.
• Ability to work under limited supervision with FDA Notified Body EU Authorized Representative and other global regulatory agencies.
• Able to manage multiple projects simultaneously.
• Proven track record of strong teamwork creatively strategic thinking.
• Ability to work well with others support regulatory activities and mentor/train others.
• Excellent written and verbal communication skills.
• Master of Science in Regulatory Affairs preferred.

Following receipt of a conditional offer of employment candidates will be required to complete additional job-related screening processes as permitted or required by applicable law.

We are an equal opportunity employer and all applicants will be considered for employment without attention to their membership in any protected class. If you require any reasonable accommodation to complete your application or any part of the recruiting process please email your request to and please be sure to include the title and the location of the position for which you are applying.