We are currently searching for a skilled professional to join a well-known client’s team as a Regulatory Affairs Associate, Jr. in Lake Forest, IL. Their work will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity.

RESPONSIBILITIES
• Supports execution of External Regulations Standards and Guidance Documents packages through tracking and monitoring ePAS packages from draft to final closure
• Prepares metrics associated with the process for Executive Management Review (EMR)
• Completes final signature approval of an ePAS package (i.e., FSG Approval)
• Data review, analysis, and verification.

EXPERIENCE
1+ year’s experience in a medical device or similarly regulated industry.

EDUCATION
Minimum of Bachelor’s Degree in science or engineering required

To be a best-fit your strengths must include:
• Strong analytical and problem-solving skills.
• Demonstrated competency and working knowledge of Excel, Word, PowerPoint, SharePoint, and Teams.
• Communicate effectively verbally and in writing. Communicate with diverse audiences and personnel. Write and edit technical documents.
• Ability to work with people from various disciplines and cultures.
• Strong attention to detail.
• Good organizational / project management skills to manage and track a wide range of tasks; ability to develop realistic action plans as well as prioritizing work activities.

Similar skillset with a more regulatory or quality experience would be beneficial.