Description
Job Summary:
Responsible for ensuring compliance of processes and documents with Good Manufacturing Practice (GMP) guidelines, guaranteeing data integrity and traceability in regulated environments.
Key Highlights:
1. Acts as a technical reference for documentation controls and data management.
2. Monitors regulatory data integrity policies and procedures.
3. Supports regulatory audits and inspections.
**Mission:**
Responsible for ensuring compliance of processes and documents with Good Manufacturing Practice (GMP) guidelines, ensuring data integrity, traceability, and reliability of data generated and maintained in regulated environments. Acts as a technical reference for documentation controls and data management, supporting internal and external audits.
**Key Responsibilities:**
* Implement and monitor data integrity policies and procedures in accordance with regulatory requirements (ANVISA, FDA, EMA).
* Review and approve GMP documentation (procedures, records, protocols, and reports), ensuring compliance with internal and regulatory standards.
* Conduct training on data integrity (ALCOA\+) and good documentation practices for operational and administrative teams.
* Perform risk assessments related to data integrity in computerized systems and manual processes.
* Monitor quality indicators related to document management and propose action plans for continuous improvement.
* Participate in projects to ensure adherence to data integrity standards (ALCOA\+).
* Support other Quality Systems activities to ensure timely manufacturing and release of products with quality for patients.
* Support regulatory audits and inspections by providing evidence and explanations regarding data and documentation controls.
**Educational Requirement**
* Completed undergraduate degree or currently in the final year
**Benefits**
* Salary advance
* Medical assistance
* Dental assistance
* Food allowance
* Meal voucher
* Gympass (Wellhub)
* Career development plan
Employment type: Permanent CLT