AtriCure, Inc.

Regulatory Affairs Specialist

AtriCure, Inc.$85K — $104K *
Mason, OH 45040In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in technical/scientific/life science required or 3+ years of Regulatory experience in the medical device industry
  • Proficient in Microsoft Office programs
  • Strong written and verbal communication skills
  • Experience in problem solving or troubleshooting
  • Minimum of 2 years in the medical device industry (preferred)
  • Basic knowledge of U.S. and European/International regulations (preferred)
  • Strong understanding of documentation within a quality management system (preferred)

Responsibilities

  • Support global regulatory pre-market applications across various regions including the U.S., EU, and Japan
  • Assist with post-market activities, including renewals and compliance updates
  • Help product marketing with international regulatory submissions and tender bids
  • Request necessary certificates for new product approvals
  • Maintain and track open regulatory requests with status updates
  • Review product changes for regulatory compliance
  • Collaborate with Regulatory Affairs staff and engineers on compliance issues
  • Maintain regulatory submission correspondence and ensure files are complete
  • Support during regulatory audits and liaise with agency reviewers

Benefits

  • Medical and Dental insurance starting on day 1
  • 401K plan with company match
  • 30 days of paid Parental Leave and additional maternity leave
  • Volunteer Time off
  • Pet Insurance
  • Access to on-site fitness center and cafeteria for corporate employees
Full Job Description
POSITION SUMMARY:

This position will originate appropriate documents to obtain and maintain marketing privileges consistent with applicable government requirements where AtriCure conducts business. This position will also maintain internal documentation of such approvals and handle requests for documentation from our international distributors and customers. This position is responsible for practicing Quality System Manual procedures and complying with its requirements, and carrying out responsibilities as outlined in safety, health and environmental policies.

ESSENTIAL FUNCTIONS OF THE POSITION:
  • Support global regulatory pre-market applications for geographies included but not limited to: Taiwan, Singapore, Australia, Brazil, Korea, UAE, EU, UK, U.S, Japan, and Canada. Submission support may include but is not limited to: IDEs, PMA submissions and supplements or 510k for US, EU Technical Documentation, and/or Japan Shonin.
  • Support global regulatory post-market activities for the responsible geographies above, such as updating 510(k) letters to file, Technical Files and Design Dossiers on an annual basis, preparing and submitting product renewals, and annual/post-approval reports.
  • Support product marketing in additional geographies, as necessary, with international regulatory submissions, product renewals, tender bids, and fulfilling custom requirements.
  • Request Certificates to Foreign government and Free Sale Certificates as new products are approved
  • Obtain notarization and legalization of documents as required
  • Maintain, update and track open regulatory requests. Provide periodic status updates on open and closed requests
  • Review of product and manufacturing changes for compliance with applicable regulations (Change Control)
  • Work with Regulatory Affairs staff, engineers and technical experts to resolve potential regulatory issues, deficiencies and questions from regulatory agencies
  • Maintain submission correspondence files and other regulatory files in a complete manner
  • Maintain regulatory files for product compliance
  • Perform other related duties as assigned in support of regulatory activities
  • Assist in interacting with reviewers from regulatory agencies on specific projects
  • Provide support during internal and external audits
  • Maintain current knowledge of worldwide regulatory requirements

ADDITIONAL ESSENTIAL FUNCTIONS OF THE POSITION:
  • Regular and predictable work performance
  • Ability to work under fast-paced conditions
  • Ability to make decisions and use good judgement
  • Ability to prioritize various duties and multitask as required
  • Ability to successfully work with others
  • Additional duties as assigned
  • Hybrid environment (with remote possibilities)
  • Travel responsibilities to AtriCure facilities for team functions and activities when needed

BASIC QUALIFICATIONS:
  • Bachelor's degree in a technical/scientific/life science discipline required or 3+ years of Regulatory experience in the medical device industry
  • Proficient on programs within Microsoft Office
  • Written and verbal communication skills
  • Problem solving and/or troubleshooting experience

PREFERRED QUALIFICATIONS:
  • Minimum of 2 years of experience in the medical device industry
  • Basic knowledge of U.S. and/or European/International regulations and standards
  • Strong understanding of documentation within a quality management system
  • Team oriented and able to effectively manage and prioritize multiple projects
  • General knowledge of medical terminology

OTHER REQUIREMENTS:
  • Ability to regularly walk, sit, or stand as needed
  • Ability to occasionally bend and push/pull as needed
  • Ability to pass pre-employment drug screen and background check
  • Occasional travel may be required


MN Hiring Range:

$85,000-104,000

#LI-JH1

AtriCure has a variety of benefits available for US based employees and their families. Examples include Medical & Dental beginning day 1 of employment, 401K plus match, 30 days of paid Parental Leave, in addition to maternity leave, for new moms and dads, Volunteer Time off, Pet Insurance, and more. Corporate-based employees also have full access to our on-site fitness center and cafeteria. To see a complete list of our benefits, please visit our careers website: https://www.atricure.com/careers-atricure/benefits.

About AtriCure, Inc.

AtriCure is a medical device company that develops and sells surgical devices used in the treatment of atrial fibrillation and other cardiac conditions. The company's products include ablation systems, left atrial appendage management devices, and other surgical instruments. AtriCure was founded in 2000 and is headquartered in Mason, Ohio. The company has a global presence, with operations in North America, Europe, and Asia.
Learn more about AtriCure, Inc.
Size
875 employees
Market Cap
$1.9 billion
Industry
Net Income
-$48.1 million
5 Year Trend
+12.1%
Revenue
$206.5 million
NASDAQ

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