We are a Brazilian pharmaceutical company dedicated to life for over 65 years. Guided by our purpose of "transforming knowledge into health," we have built our history with boldness, innovation, and visionary spirit. **Our reason for being** is to promote high-quality health so that people can enjoy every moment. We offer a broad portfolio of medications across multiple specialties—including gynecology, oncology, and cardiology—to comprehensively and individually meet patients’ needs with efficient and innovative formulations. We market over 100 brands in more than 200 presentations. **We want you to find your place here!** According to GPTW, we are recognized as an excellent workplace. We foster transparent and trusting relationships with our 3,000+ employees and encourage mobility as a professional development tool. Health and well-being guide our decisions. **\#BecauseLifeIsTreated** **Responsibilities and duties** **On a day-to-day basis, you will:** * Plan, develop, and execute Process Validation studies, including protocol and report development and updates, risk assessments, and evaluations—ensuring regulatory compliance and technical robustness. * Conduct on-site monitoring of validation study stages, ensuring adherence to defined requirements and recording necessary evidence. * Perform sampling for Process Validation studies, ensuring traceability, compliance with sampling methods, and alignment with the analytical plan. * Support continuous monitoring routines and periodic validation reviews, evaluating trends and the need for revalidation. * Develop and review cleaning validation protocols and reports, where applicable. * Draft product lifecycle documents, such as Product Quality Reports (PQR) and * Continuous Process Verification (CPV). * Conduct impact assessments arising from changes, deviations, or process updates, determining revalidation requirements. * Collaborate with production, engineering, and quality departments to ensure state of control, traceability, and adherence to validation requirements. * Participate in validation-related investigations (e.g., deviations, Out-of-Specification results, and nonconformities), proposing corrective actions aligned with Good Practices. * Contribute to risk analyses applied to validation (e.g., FMEA, Irisk, and other methodologies) as decision-making tools. * Support projects and routines involving aseptic processing, ensuring alignment with Good Manufacturing Practices (GMP) and applicable regulatory guidelines. * Assist in internal and external audits by providing evidence and technical explanations regarding the validation program and adopted strategies. **Requirements and qualifications** **To participate in our selection process:** * Currently pursuing a degree in Pharmacy, Chemical Engineering, Production Engineering, or related fields. * Basic experience or internship in Process Validation or Quality Systems is desirable. * Introductory knowledge of risk analyses (e.g., FMEA, HACCP), process variability and control concepts, and Process Validation stages. * Introductory knowledge of PQR and CPV. * Desirable experience with technical documentation structure (protocols and reports) within quality systems. **You will stand out if you have:** * Knowledge of applicable regulatory guidelines (e.g., RDC 658/2022, EU GMP, FDA). * Experience—even academic—with statistical tools or data analysis applied to processes. * Familiarity with CPV and the validation lifecycle. * Experience working in regulated environments (particularly pharmaceutical). * Basic knowledge of quality systems (e.g., deviations, CAPA, Change Control, Product Quality Review). **Additional information** **\+ Additional details** Work location (Base): Embu das Artes Working hours: Monday to Friday – Second Shift (Flexible schedule) **For Libbs employees** * Applications accepted until **05/27/2026** * Preferred qualifications may be prioritized during candidate selection for the next stage. * Simultaneous participation in different internal selection processes is not permitted. **Benefits for you!** * Meal voucher; * Food voucher; * 100% discount on Libbs medications; * Pharmacy benefit – Vidalink; * Profit Sharing Program (PPR); * Parking, transportation voucher, or shuttle service (applicable for shift-based roles and subject to availability of routes serving regions located within a straight-line radius of up to 40 km from the facility); * USE Program: subsidy for purchasing equipment used for work, which may also be used for personal purposes; * Flexible benefits (TotalPass, life insurance, private pension, medical and dental assistance, food allowance). We are a Brazilian pharmaceutical company dedicated to life for over 67 years. Guided by our purpose of "transforming knowledge into health," we have built our history with boldness, innovation, and visionary spirit. Here, we believe that **diversity** strengthens our purpose and our relationships. All positions are evaluated with an inclusive focus, respecting competency-based assessment. **Our reason for being** is to promote high-quality health so that people can enjoy every moment. We offer a broad portfolio of medications across multiple specialties—including gynecology, oncology, and cardiology—to comprehensively and individually meet patients’ needs with efficient and innovative formulations. We market over 100 brands in more than 240 presentations. **We want you to find your place here!** According to GPTW, we are recognized as an excellent workplace. We foster transparent and trusting relationships with our 3,900+ employees and encourage mobility as a professional development tool. Health and well-being guide our decisions. We operate a manufacturing unit in Embu das Artes, logistics centers in Embu and Varginha, and our administrative team works fully remotely, with access to coworking spaces worldwide.
João Silva
Indeed · HR
João Silva
Indeed · HR
