Description
**Job Description:**
Grupo Seres, in partnership with a national pharmaceutical industry company, is seeking a professional to work as a JUNIOR QUALITY ANALYST (SYSTEM VALIDATION)
**Responsibilities:**
Perform validation service activities related to the qualification of computerized systems (hardware, software, programmable logic controllers – PLCs, and electronic spreadsheets), in compliance with Good Manufacturing Practices (GMP) requirements established by ANVISA, WHO, and other national and international regulatory bodies; contribute to the smooth execution and monitoring of implemented processes; ensure timely fulfillment of demands from both the Quality department and interfacing departments; support continuous improvement of processes and products—either through identification/proposal of actions or execution of planned actions; and perform other departmental tasks related to System Acceptance Testing (SAT), User Requirements Specifications (URS), Change Control, Risk Assessment, development of Standard Operating Procedures (SOPs), and training, thereby facilitating adherence to Good Manufacturing Practices.
**Working Hours:**
**Schedule:** 8:00 AM to 5:00 PM
**Shift:** Monday to Friday (1-hour lunch break)
**Work Model:** On-site
**Work Location:**
Jacaerpaguá, RJ\- Brazil
We encourage applications from persons with disabilities (PCD), Black individuals, women, and LGBTQIAPN\+ individuals.
**Requirements:**
**Mandatory Qualifications:**
Bachelor’s degree completed in Pharmacy, Chemistry, or Chemical Engineering;
Brief experience in the pharmaceutical or related manufacturing industry involving quality management systems;
Proficiency in Microsoft Office suite, especially Excel (intermediate level or higher);
Intermediate-level English proficiency;
**Desirable Qualifications:**
Knowledge of computerized system validation and/or equipment qualification is desirable.