Edwards Lifesciences Corp

Specialist, Regulatory Affairs Surgical

Edwards Lifesciences Corp$74K — $104K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree with 3 years of relevant experience or equivalent qualifications
  • Formal training in government or trade associations recommended
  • Degree in a scientific field such as Biology, Microbiology, Chemistry, or Bioengineering preferred
  • Experience with domestic and international product submissions
  • Strong understanding of global regulations for Class II and III medical devices

Responsibilities

  • Represent regulatory function on manufacturing and development teams
  • Prepare and oversee documentation for global regulatory submissions
  • Provide guidance on regulatory requirements for contingency planning
  • Monitor and assess global regulations impacting projects
  • Review labeling and product documentation for compliance
  • Prepare necessary documents for global regulatory bodies

Benefits

  • Competitive salaries and performance-based incentives
  • Diverse benefits programs for employees and families
Full Job Description
How you will make an impact:
  • Represent the regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regulatory requirements and resolving conflicts between those requirements and development issues, and/or reporting to management
  • Prepare and oversee documentation packages for submission to global regulatory agencies. Track timelines and documents milestone achievements for inclusion in regulatory submissions. May interact with regulatory agencies as part of submission review and on-site audit support (e.g., IDE's, PMA's, annual reports, 510(k)'s, STED's and CE marking design dossiers and technical files)
  • Provide guidance on regulatory requirements necessary for contingency planning
  • Monitor proposed and current global regulations and guidance; assesses impact of such regulations and guidance on assigned project(s); proposes suggestions on utilizing regulatory updates to expedite approval process
  • Review labeling content, product and process changes, and product documentation to assure regulatory requirements compliance, consistency, and accuracy
  • Prepare documents for submissions, including assuring the appropriate forms for all of the global regulatory bodies; assist with GUDID submissions


What you will need (Required):
  • Bachelor's Degree & a minimum of 3 years related experience or equivalent experience based on Edwards criteria
  • Coursework, seminars, and/or other formal government and/or trade association training


What else we look for (Preferred):
  • Bachelor's Degree in scientific discipline (e.g., Biology, Microbiology, Chemistry, Bioengineering)
  • Experience in preparing domestic and international product submissions
  • Solid knowledge and understanding of global regulations relevant to medical devices, Class II and/or Class III devices
  • Solid knowledge and understanding of global regulatory requirements for new products or product changes


Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.

For California, the base pay range for this position is $74,000 - $104,000 (highly experienced).

The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.

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About Edwards Lifesciences Corp

Edwards Lifesciences is an American medical technology company headquartered in Irvine, California, specializing in artificial heart valves and hemodynamic monitoring. It developed the SAPIEN transcatheter aortic heart valve made of cow tissue within a balloon-expandable, cobalt-chromium frame, deployed via catheter. The company has manufacturing facilities at the Irvine headquarters, as well as in Draper, Utah; Costa Rica; the Dominican Republic; Puerto Rico; and Singapore; and is building a new facility due to be completed in 2021 in Limerick, Ireland.
Learn more about Edwards Lifesciences Corp
Size
15,700 employees
Market Cap
$45.6 billion
Industry
Net Income
$823.4 million
Founded
1958
5 Year Trend
+12%
Revenue
$4.3 billion
NASDAQ

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