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Regulatory Affairs Specialist

Remote / Online - Candidates ideally in
Willows, Glenn County, California, 95988, USA
Listing for: Placements24
Remote/Work from Home position
Listed on 2026-09-27
Job specializations:
  • Pharmaceutical
    Healthcare Compliance, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 90000 - 140000 USD Yearly USD 90000.00 140000.00 YEAR
Job Description & How to Apply Below
Location: Willows

About the Role

Our client is seeking a meticulous and proactive Regulatory Affairs Specialist to support their operations from Welkom . This role is essential for ensuring that all pharmaceutical products meet stringent regulatory requirements for approval and marketing in various global markets. You will be responsible for preparing and submitting regulatory documentation, liaising with health authorities, and staying abreast of evolving regulations. This is a fully remote position, offering you the flexibility to manage your work effectively while contributing to critical compliance activities.

We are looking for an individual with a keen eye for detail and a solid understanding of pharmaceutical regulatory landscapes.

Key Responsibilities
  • Prepare, review, and submit regulatory submissions (e.g., INDs, NDAs, MAAs) to health authorities globally.
  • Ensure compliance with all applicable regulatory requirements, guidelines, and company policies.
  • Liaise effectively with regulatory agencies during the submission and review process.
  • Monitor and interpret new and evolving regulations and guidance documents, assessing their impact on the company's products and operations.
  • Maintain regulatory documentation and databases, ensuring accuracy and completeness.
  • Collaborate with cross-functional teams, including R&D, Quality Assurance, and Marketing, to provide regulatory guidance and support.
Requirements
  • Bachelor's degree in a scientific discipline (e.g., Pharmacy, Chemistry, Biology) or a related field.
  • Proven experience in Pharmaceutical Regulatory Affairs.
  • Demonstrated experience in preparing and submitting various types of regulatory dossiers.
  • Thorough understanding of global regulatory requirements and guidelines (e.g., FDA, EMA).
  • Excellent written and verbal communication skills, with strong attention to detail.
  • Ability to work independently and manage multiple projects effectively in a remote setting.
Benefits
  • Competitive annual salary with performance incentives.
  • Comprehensive health, dental, and vision benefits package.
  • Generous paid time off and holidays.
  • Professional development programs and opportunities to attend industry conferences.
  • A supportive and collaborative remote work environment.
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