Title: Medical Writer II
Location: Des Plaines, IL
Duration: 10+ Months
100% Onsite
Job Description
Focus Area: EU IVDR Compliance
We are seeking a detail-oriented professional to join our team in an onsite capacity, with a primary focus on supporting EU In Vitro Diagnostic Regulation (IVDR) activities.
Key Qualifications
- Education: A bachelor's degree in a science-related field is required.
- Expertise: Strong understanding of EU IVDR regulatory requirements and documentation processes.
- Skills: Proficiency in Microsoft Word and Excel is essential.
Responsibilities
- Develop, review, and finalize regulatory documents to support EU IVDR submissions.
- Verify and proofread work to ensure accuracy, completeness, and compliance with applicable standards.
- Collaborate with cross-functional teams to align regulatory documentation with project goals.
This role offers an excellent opportunity to contribute to high-impact regulatory submissions in a fast-paced, collaborative environment.
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.
