Hiring.Camp

RA Specialist III - Temporary Non-Employee

Biorad

·

Yesterday

Salary
$60+
Location
Irvine, CA, US
Type
Temporary
Experience
5+ years
Education
Bachelor
Closing date
Today
Source
iCIMS

Description

Overview

Bio-Rad is looking for a Regulatory Affairs Specialist III to join our Irvine, CA office. In this position you will support new product developments/product modifications, IVDR implementation, and international product registrations. This is a temporary role projected to end March 1, 2027.

Perform other Regulatory Affairs responsibilities and special projects as assigned.

 

How you will make an impact:

 

  • Manage global regulatory submissions, registrations, renewals, and maintenance activities to support new and modified products across international markets.
  • Ensure product claims, labeling, IFUs, and supporting documentation meet applicable global regulatory requirements.
  • Coordinate responses to regulatory authority questions and information requests with cross-functional partners.
  • Manage Regulatory Affairs change requests and maintain audit-ready records.
  • Maintain technical documentation to support CE Marking and applicable regulatory requirements.
  • Coordinate labeling changes and communicate updates to regions and stakeholders.
  • Manage SAP product restrictions to ensure regulatory compliance.
  • Perform other Regulatory Affairs responsibilities and special projects as assigned.

 

 

What you bring: 

 

  • Bachelor's degree in Biology, Chemistry, Medical Technology, or a related scientific discipline.
  • Advanced degree and/or Regulatory Affairs Certification (RAC) preferred.
  • 5 + years of experience in domestic and international regulatory affairs or regulatory compliance, preferably within the in vitro diagnostics (IVD) industry.
  • Extensive knowledge of global regulatory requirements, including FDA, NPMA and IVDR.
  • Extensive knowledge of product labeling requirements and international product registration processes.
  • Strong customer focus with the ability to support cross-functional and external stakeholders.
  • Detail-oriented with strong technical and regulatory writing skills.
  • Proficient in computer applications, including Quality Manament systems such as SAP.
  • The ability to perform basic statistical analysis.
  • Strong analytical, communication, problem solving, and critical thinking skills.
  • Demonstrated ability to multitask and manage competing priorities across multiple timelines

 

Pay Rate $60.00 per hour

Schedule 8 am - 5 pm Monday to Friday

Assignment Duration - 6 months

Skills

SAPFDACompliance