RA Specialist I - Temporary

Provide regulatory support for IVD products with multiple product groups with clinical diagnostics.

Assembles low to medium complexity regulatory submissions to support world wide product registration change requests for IVDR.

Basic analytical, communication, problem solving, and critical thinking skills to meet daily job responsibilities.

Interface daily with desktop publisher, technical writers and regulatory specialists.

Work collaboratively with R & D, QA, Planning and Manufacturing teams.

• Strong prioritization skills, flexibility and ability to handle multiple projects simultaneously while meeting deadlines
• Ability to communicate effectively with employees across multiple departments
• Highly organized and detail-oriented. Good time management.
• Technical aptitude for understanding IVD product features
• Understanding of databases and electronic systems.

• Education:BS in Biology or other scientific field
• Work Experience: 6 mo -2 years experience in IVD regulatory affairs.
• Proficient use of MS Office applications (e.g., Excel, Word, PowerPoint, Teams)
• Laboratory research experience in an IVD medical device regulated environment is strongly preferred.
• Understanding of scientific reports, risk management, Quality Systems

Compensation : The estimated hourly range for this position is $32.00 to $35.00 per hour at the time of posting.

Actual compensation will be provided in writing at the time of offer, if applicable, and is based on several factors we believe fairly and accurately impact compensation, including geographic location, experience, knowledge, skills, abilities, and other job permitted factors.

As a temporary associate, your employment will be managed directly through our approved agency provider.

Who We Are: For 70 years, Bio-Rad has focused on advancing the discovery process and transforming the fields of science and healthcare.