Regulatory Affairs Specialist

Há 4 dias


São Paulo, São Paulo, Brasil Quality Compliance Tempo inteiro
Job Title: Regulatory Affairs Specialist

At Quality Compliance, we are seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory team, you will be responsible for ensuring compliance with ANVISA and international standards.

Key Responsibilities:

* Prepare and submit regulatory documentation in compliance with ANVISA requirements
* Collaborate with cross-functional teams to ensure compliance and efficient submissions
* Manage pharmaceutical equivalence studies and ensure adherence to REBLAS Labs' protocols
* Oversee and manage regulatory timelines, submission commitments, and agency interactions
* Ensure all regulatory submissions align with industry standards, policies, and timelines

Requirements:

* Bachelor's degree in Pharmacy
* Master's degree in Regulatory Affairs or similar courses
* Certificate in Advanced English

Location:

São Paulo/SP

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