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Regulatory Affairs Associate

3 months ago

Lake Bluff, United States GForce Life Sciences Full time

Regulatory Affairs Associate -- On-site in Abbott Park, IL

Must be able to work on a W2

Job Summary: We are seeking a dedicated Regulatory Affairs Associate to join our team. In this role, you will support the preparation and submission of regulatory documents to ensure compliance with all applicable regulations. The ideal candidate will have a keen attention to detail and strong communication skills to effectively interact with regulatory bodies and internal stakeholders.

Job Responsibilities:

  • Prepare, review, and submit regulatory documents to ensure compliance with relevant regulatory requirements.
  • Maintain up-to-date knowledge of regulatory guidelines and industry standards.
  • Collaborate with cross-functional teams to gather necessary documentation for regulatory submissions.
  • Monitor and track regulatory submission timelines and provide updates to project teams.
  • Assist in the development and implementation of regulatory strategies.
  • Support audits and inspections by regulatory authorities.
  • Maintain regulatory files and databases, ensuring all documentation is accurate and up-to-date.

Job Requirements:

  • Bachelor’s degree in life sciences, pharmacy, or a related field.
  • 2+ years of experience in regulatory affairs within the pharmaceutical, biotechnology, or medical device industry.
  • Knowledge of regulatory guidelines and submission processes.
  • Strong attention to detail and organizational skills.
  • Excellent written and verbal communication skills.
  • Ability to work independently and as part of a team.
  • Proficiency in Microsoft Office Suite and regulatory databases.

Term and Start

  • 8 month contract
  • On-site in Abbott Park, IL
  • Pay rate: $26-30/HR