Job Summary: A professional to support computerized system validation in the pharmaceutical industry, ensuring compliance with GMP. Key Highlights: 1. Essential support in GxP system validation 2. Focus on technical learning and development 3. Work in a multidisciplinary environment We are seeking committed professionals with industrial (pharmaceutical) experience and willingness to grow alongside the project. **Job Objective** Support computerized system validation (CSV) activities, ensuring that systems used in GxP environments are properly documented, tested, and controlled per Good Manufacturing Practices (GMP), under the guidance of more experienced professionals. **Main Responsibilities** \- Support the preparation, organization, and review of validation documentation: URS, Risk Assessments, IQ, OQ, PQ, and reports; \- Execute qualification and validation tests per approved protocols; \- Record test evidence traceably (screenshots, logs, checklists, audit trails); \- Support verification of access controls, security, backup, and data integrity; \- Assist in system version control and change management; \- Support supplier and system integrator oversight during testing and validation; \- Assist in reviewing Standard Operating Procedures (SOPs) related to systems; \- Contribute to organizing validation dossiers and documentary traceability. **Technical Requirements** \- Completed or ongoing undergraduate degree in Engineering, Pharmacy, or related fields; \- Basic knowledge of GMP; \- Familiarity with computerized system validation (CSV) – experience is a plus; \- Basic knowledge of Data Integrity; \- Familiarity with IT environments, industrial software, or laboratory systems (desirable); \- Advanced Excel and technical documentation skills; \- Spreadsheet software proficiency – experience is a plus. **Behavioral Competencies** \- Organization and attention to detail; \- Analytical and disciplined profile; \- Ability to learn technical concepts quickly; \- Strong communication skills and professional demeanor; \- Ability to work effectively in a multidisciplinary environment. **Level of Autonomy** Perform tasks with solid technical autonomy, under direct supervision of mid-level and senior analysts, with emphasis on learning and technical development. **Expected Performance Indicators** \- Correct execution of tests per protocols; \- Quality and traceability of documentary evidence; \- Adherence to validation timelines; \- Reduction of rework and inconsistencies; \- Technical progress throughout the contract duration. **Location and Employment Terms** Work Location: Santana de Parnaíba \- SP Work Mode: On-site Employment Type: PJ \- Initial 12-month term (possible renewal) Salary Range: R$ 4\.500 to R$ 5\.500, depending on knowledge/experience CNPJ required for invoice issuance (MEI accepted) Job Type: Permanent CLT Compensation: R$4\.500,00 \- R$5\.500,00 per month Work Location: On-site