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Temporary Record Label Internships Jobs in Riverside, CA

Fairway Staffing Solutions

Receiving

Irvine, CA · On-site

$18/hr

Temp to HirePosition Summary:The Quality Control / Shipping Associate is responsible for performing ... system records. This role requires strong attention to detail, computer proficiency, and the ...

Kiewit

Kiewit Scholars - Summer 2027 Internship

Irvine, CA · On-site

$18 - $23.25/hr

Intern Market: Transportation Employment Type: Full Time Temporary Position Overview Are you ... Our successful track record in the transportation market includes the construction and upgrade of ...

ABA Industry Inc

Logistics support associate

Ontario, CA · On-site

$19 - $23/hr

Carson, CA (temporary) → Ontario, CA (expected to start Mid October, 2026) We are seeking a ... Verify outbound shipments for correct items, quantities, pallet counts, and labels * Receive ...

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Infographic showing various Temporary Record Label Internships job openings in Riverside, CA as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 16% Part Time, and 3% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution.

RA Specialist III - Temporary Non-Employee

Bio-Rad Laboratories, Inc.

Irvine, CA • On-site

$60/hr

Temporary

Posted 2 days ago

New

Bio-Rad Laboratories rating

7.0

Company rating: 7.0 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

73rd of 103 rated chemical manufacturers

Job description

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

Legal Entity: (USA_1000)Bio-Rad Laboratories, Inc.

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