Junior Equipment Management and Metrology Analyst

Description

Job Summary: Professional to serve as a Junior Equipment Management and Metrology Analyst, performing activities related to equipment management, calibration, and qualification. Key Highlights: 1. Management, calibration, and qualification of equipment and instruments. 2. Development and revision of procedures and work instructions. 3. Technical support and development in a supervised environment. **Job Description:** The Seres Group, in partnership with a national pharmaceutical company, is seeking a professional to serve as a Junior Equipment Management and Metrology Analyst. **Responsibilities:** Proactively execute, within the Metrology Service, responsibilities related to equipment and measurement instrument management, calibration, and qualification; provide technical support for low-complexity and low-criticality activities, with increasing accountability under supervision by more experienced professionals; develop and revise procedures and work instructions for equipment management, maintenance, and calibration in accordance with national and international standards and guidelines; conduct training on SOPs and integrate new employees into service activities; control measurement instruments and equipment according to defined methods and procedures; create and maintain updated registries; schedule and monitor calibration, maintenance, and qualification plans—including opening, updating, and closing service orders; coordinate with internal and external service providers for preventive and corrective maintenance, calibration, and qualification of equipment and monitor their execution; support the preparation of User Requirements Specifications (URS) for new equipment and systems; support the evaluation and archiving of calibration and qualification protocols; assist in the installation and adaptation of new equipment and computerized systems in laboratories; operate internal systems; perform critical analyses of procedures; prepare technical opinions and result reports; control and archive technical documentation; record executed activities; contribute to smooth departmental operations and timely fulfillment of requirements; collaborate on change control, deviation handling, and risk analysis associated with qualification to ensure compliance with Good Manufacturing Practices (GMP) and institutional policies. **Working Hours:** **Schedule:** 8:00 AM to 5:00 PM **Work Week:** Monday to Friday **Work Model:** On-site Other observations if necessary **Work Location:** Jacarepaguá, Rio de Janeiro \- Brazil We encourage applications from persons with disabilities (PCD), Black individuals, women, and LGBTQIAPN\+ community members. **Requirements:** **Mandatory Requirements:** Bachelor’s degree completed in Engineering, Pharmacy, Chemistry, Biological Sciences, Quality Management, Industrial Production Management, or related fields; Experience and knowledge of calibration of equipment and measurement instruments; Experience in preparing technical documentation (reports, procedures, work instructions, or others); Proficiency with Microsoft Office suite. **Desirable:** Knowledge of pressure, temperature, humidity, velocity, weight, and glassware instruments, as well as equipment such as HPLC, UHPLC, Dissolution Tester, GC, etc.