Regulatory Affairs Consultant - Chicago

Only for registered members Chicago, United States

1 month ago

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Job summary

Develop global regulatory strategies for medical device products to meet business objectives and collaborates across a matrixed organization to ensure global success of products registration.

Responsibilities

  • Negotiate with regulatory authorities to resolve questions/issues that arise during the product lifecycle.
  • Maintenance of Regulatory Affairs product files and ensure compliance with regulatory requirements.

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