Analista pl da qualidade – Paulínia/SP
Efetivo (CLT)
Responsabilidades
- Ensure Good Practices (GxP) are followed and that results meet quality standards.
- Support the creation, implementation, and maintenance of the Quality Management System for R&D.
- Draft and review procedures, work instructions, and area policies.
- Review study data/batch records and prepare dossiers for product release.
- Participate in internal audits and support the implementation of corrective actions.
- Assist with activities related to Clinical Research, ensuring regulatory and documentation compliance.
- Interact with development laboratory teams and other departments to ensure alignment with quality standards.
Requisitos
- QUALIFICAÇÕES MÍNIMAS
- Education: Degree in Veterinary Medicine, Pharmacy, Chemistry, or Biology.
- Experience with quality management systems (preferably in the pharmaceutical industry).
- Knowledge of technical documentation review and regulatory processes (MAPA).
- QUALIFICAÇÕES PREFERENCIAIS
- Familiarity with internal audits and Good Clinical Practices.
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