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Regulatory Affairs Associate

$40 - $45 per hour

Experis/Manpower Group

Job Title: Regulatory Affairs Associate

Location: Alameda, CA

Work Arrangement: 100% Onsite

Duration: 12 Months
Pay Range: $40 - $45 per hour (W2)

We are seeking a "Regulatory Affairs Associate" to join one of our leading healthcare clients.

Position Overview
We are seeking a Regulatory Affairs Associate to support the Regulatory Affairs team by reviewing labeling, advertising, and promotional materials, ensuring regulatory compliance, supporting regulatory submissions, and collaborating with cross-functional teams. This role also supports new product introductions (NPI) and post-market regulatory activities.

Key Responsibilities
  • Review labeling, advertising, and promotional materials for regulatory compliance.
  • Partner with Marketing to provide regulatory guidance and approval support.
  • Support regulatory submissions, including 510(k), PMA, Health Canada, and Latin America submissions.
  • Assist with NPI and post-market regulatory activities.
  • Develop and review Regulatory Affairs SOPs.
  • Communicate regulatory requirements to cross-functional teams.
  • Prepare and maintain regulatory documentation.
Required Qualifications
  • Bachelor's degree or equivalent experience.
  • Minimum 2 years of experience in a regulated industry (Medical Device, Pharmaceutical, Nutrition, or Food).
  • Regulatory Affairs experience preferred; Quality, R&D, Scientific Affairs, or Operations experience will also be considered.
  • Strong written and verbal communication skills.
  • Excellent analytical, project management, and organizational skills.
  • Strong attention to detail and ability to work collaboratively.
Preferred Qualifications
  • Bachelor's degree in a scientific, engineering, medical, or Regulatory Affairs discipline.
  • 1+ year of Regulatory Affairs or Quality experience within the Medical Device industry.
  • Experience reviewing labeling, advertising, or promotional materials.
  • Knowledge of FDA regulations, Medical Device Quality Systems, Design Controls, and international regulatory requirements.
  • RAC certification is a plus.
  • Proficiency with Microsoft Word, Excel, PowerPoint, Visio, and SharePoint.

We are looking for the candidate who are eligible to work with any employers without sponsorship .

If you're interested, please click "Apply" button.
Vacancy posted 22 hours ago
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