Senior Regulatory Affairs Specialist

Title: Senior Regulatory Affairs Specialist

Location: Lake forest, IL

Duration: 12+ months contract

100% Onsite

Qualifications:

• At least 5 year's work experience in Regulatory Affairs, Quality, or related field experience; Less experience may be appropriate with advanced degree.
• Preferred experience in the Healthcare industry.

Preferred:

• Experience in Design Control, Regulatory documentation and new product development preferred.
• Medical device or in-vitro diagnostics experience strongly desired
• Knowledge of regulations and standards affecting IVDs and Biologics is preferred – Post Market Surveillance
• Experience with site audits preferred
• Experience and proficiency with Microsoft applications (Word, Excel, PowerPoint etc.)
• Abbott experience
• Experience with Technical Writing

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.

Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.