Technical Documentation Analyst
Posted 2ds ago
Employment Information
Report this job
Job expired or something wrong with this job?
Job Description
Technical Analyst evaluating regulatory documentation for raw materials and packaging. Ensuring compliance with Brazilian laws and international regulatory standards in the P&D process.
Responsibilities:
- Perform technical-regulatory evaluation of documentation from raw material and packaging manufacturers, including critical analysis and follow-up on requests for additional technical information;
- Technically assess all R&D documentation that makes up dossiers for the notification of pharmaceuticals, cosmetics, foods and dietary supplements, ensuring adherence to current Brazilian legislation, ANVISA standards and international regulatory references;
- Serve as the interface between R&D and Regulatory Affairs, ensuring alignment and consistency of technical documentation prepared for regulatory dossiers;
- Ensure standardization, organization and traceability of technical documentation produced by the R&D area;
- Participate in continuous improvement initiatives for document and regulatory processes, contributing to compliance plans in response to legislative updates and requirements issued by ANVISA;
- Provide technical support for responses to regulatory requests related to the notification processes for pharmaceuticals, cosmetics, foods and dietary supplements, especially on matters related to R&D documentation.
Requirements:
- Bachelor's degree in Pharmacy, Chemistry, Biomedicine, Nutrition, Biology, Food Engineering, Business Administration or related fields;
- Previous experience with technical and/or regulatory documentation;
- Experience interfacing between R&D and Regulatory Affairs;
- Knowledge of ANVISA regulations applicable to the notification and regularization of pharmaceuticals, cosmetics, foods and dietary supplements;
- Technical knowledge of nutrients, additives, ingredients and raw materials;
- Familiarity with international legislation and guidance related to the pharmaceuticals, cosmetics, food and dietary supplement sectors;
- Experience preparing and reviewing regulatory dossiers is desirable.


















