Regulatory Compliance Specialist

4 weeks ago


Houston, Texas, United States Medasource Full time

Job Overview:

Medasource is seeking a highly skilled Regulatory Affairs Consultant to join our team. As a key member of our regulatory team, you will be responsible for leading and coordinating regulatory submissions, developing regulatory strategies, and ensuring compliance with relevant regulations.

This is a challenging and rewarding role that requires strong analytical and communication skills. If you have a passion for regulatory affairs and a desire to work in a dynamic and growing company, we encourage you to apply.

Key Responsibilities:

  • Develop and implement regulatory strategies for investigational and marketed products
  • Compile and submit regulatory documents to the FDA and other Health Authorities
  • Maintain accurate and up-to-date records of regulatory submissions and approvals

Requirements:

  • Bachelor's degree in life sciences or related field
  • Master's degree preferred
  • Six years of Regulatory Affairs experience within an FDA-regulated industry, preferably devices, diagnostics, or pharmaceuticals

Compensation and Benefits:

Our estimated salary range for this position is $120,000 - $160,000 per year, depending on experience. We also offer a comprehensive benefits package, including health insurance, retirement plan, and paid time off.



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