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Temporary Entry Level Regulatory Affairs Jobs (NOW HIRING)

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Entry-Level Regulatory Affairs Associate Location: South Portland, ME Pay: $20-$23 per hour Schedule: Monday-Friday, 7:00 AM-4:30 PM We are seeking an Entry-Level Regulatory Affairs Associate to ...

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Temporary to Hire opportunity. Paying $32-36/hr, depending on qualifications. Hours are 9:00 AM - 5 ... The Regulatory Affairs Associate is an entry-level position for an individual committed to ...

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The Regulatory Affairs Associate is an entry-level position for an individual committed to developing a career in Regulatory Affairs. The role supports Regulatory Affairs activities primarily for ...

NY · On-site

$68.51 - $102.76/hr

Temps Pleinposted on: Publié aujourd'huijob requisition id: R2612110Cherchez-vous à faire une ... Regulatory Affairs Manager - Poland** to support regulatory strategy, submissions, lifecycle ...

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This is an entry-level/early-career Regulatory Affairs opportunity supporting the IVDR (In Vitro Diagnostic Regulation) group . The Regulatory Affairs Associate will assist with regulatory ...

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This is an entry-level/early-career Regulatory Affairs opportunity supporting the IVDR (In Vitro Diagnostic Regulation) group . The Regulatory Affairs Associate will assist with regulatory ...

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Temporary Entry Level Regulatory Affairs information

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$34

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How much do temporary entry level regulatory affairs jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for temporary entry level regulatory affairs in the United States is $34.60, according to ZipRecruiter salary data. Most workers in this role earn between $22.36 and $26.20 per hour, depending on experience, location, and employer.

What are the most commonly searched types of Temporary Regulatory Affairs jobs?

The most popular types of Temporary Regulatory Affairs jobs are:

Entry-Level Regulatory Affairs Associate

Collaborative LLC

South Portland, ME • On-site

$20 - $23/hr

Full-time

Medical, Dental, Vision

Posted 3 days ago

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Job description

Entry-Level Regulatory Affairs Associate

Location: South Portland, ME
Pay: $20–$23 per hour
Schedule: Monday–Friday, 7:00 AM–4:30 PM


We are seeking an Entry-Level Regulatory Affairs Associate to support regulatory activities in a medical device environment.


This is an excellent opportunity for someone who is new to Regulatory Affairs and wants to build experience in a highly regulated industry. The ideal candidate is organized, detail-oriented, comfortable working with documents and computer systems, and able to follow procedures accurately.


Prior Regulatory Affairs experience is not required.


Job Summary

  • Assist with organizing and preparing regulatory documents and submission materials
  • Support the preparation of regulatory submission and registration packages
  • Review documents for accuracy, completeness, and consistency
  • Maintain electronic and paper regulatory records
  • Track regulatory requests, submissions, and project timelines
  • Assist with updating product listings, registrations, licenses, and approvals
  • Help prepare routine regulatory reports and communications
  • Research regulatory requirements and procedures as directed
  • Assist with document quality control
  • Maintain tracking and document management systems
  • Support post-market regulatory activities
  • Prepare and organize documentation for registrations and other regulatory purposes
  • Work with internal teams to gather and organize required information
  • Follow established procedures, templates, and regulatory guidelines
  • Help ensure regulatory activities are completed accurately and on schedule


Qualifications

  • High school diploma or equivalent required
  • Approximately 1 year of work experience preferred
  • No prior Regulatory Affairs experience required
  • Strong attention to detail and organizational skills
  • Ability to work with detailed documents and information
  • Strong written and verbal communication skills
  • Comfortable using computers and electronic document systems
  • Ability to follow procedures and instructions carefully
  • Ability to manage multiple tasks and meet deadlines


Ideal Backgrounds

Candidates with experience in the following areas may be a strong fit:

  • Quality Control or Quality Assurance
  • Document Control or Documentation
  • Administrative or Records Support
  • Medical Device or Pharmaceutical Manufacturing
  • Manufacturing or Production
  • Healthcare or Clinical Support
  • Laboratory environments
  • Data Entry or detail-oriented office roles


Experience working with SOPs, controlled documents, records, quality processes, compliance requirements, or tracking systems is a plus.


If you have a strong attention to detail and are looking to begin a career in Regulatory AffairsQuality, or a related field, apply today!