Nayane Ferreira Da Silva

- Recorded laboratory results into the StarLims system, ensuring accuracy and completeness.

- Prepared monthly reports and summaries, interpreting test results for submission to the Ministry of Environment.

- Assisted in air emission calculations, documentation, and external/internal emission audits.

- Collaborated with government representatives, employers, and the public on health, environmental, and safety issues.

- Monitored emission control devices to ensure compliance with regulations.

- Contributed to the re-certification of the Smelter through ISO 9001, 14001, and Aluminium Stewardship Initiative (ASI) audits.

- Conducted background research and analysis, supporting permit amendments and new project requirements.

- Developed indicators, procedures, spreadsheets and other documents for the HSE department in accordance with company's templates, that required advanced Microsoft application skills (Word, Excel, PowerPoint, Outlook).

- Managed stock, inventory corrections, and data entry.

- Provided quality care to customers and trained new staff.

- Ensured compliance with workplace safety and confidentiality guidelines.

- Supported pharmacists in prescription preparation and inventory audits.

- Provided office support by printing, scanning and collecting data from customers with accuracy.

- Conducted audits of partners' facilities and documentation to verify compliance with regulations and quality standards.

- Assisted partners in achieving ISO and GMP certification requirements.

- Planned and performed over 30 audits of Good Manufacturing Practices.

- Monitored changes in relevant regulations and reported compliance issues to management.

- Facilitated communication with stakeholders to build positive relationships.

- Oversaw the disposal of non-compliant products, materials, and equipment.

- Implemented a Supplier Qualification program, reducing deviations by 15%.

- Managed document control, including incident reports, deviation investigations, and change management.

- Reviewed and approved quality department procedures and provided training.

- Evaluated and approved suppliers based on legal requirements and quality standards.

- Investigated and reported internal quality deviations during production.

- Contributed to batch release record evaluation and management of changes.