**Kivalita Consulting** is a consulting firm specialized in quality and technology for the **Life Science** sector — pharmaceutical, cosmetic, chemical, and medical devices. Operating in the market for 10 years, we doubled in size between 2019 and 2025 and continue expanding internationally. Our purpose is to transform quality management into a strategic advantage for our clients — always with ethics, positive impact, and inclusion. Here, every professional is a **Kivalita Lion**, the protagonist of our growth. We are seeking a **Junior Quality Control Analyst**, technically skilled, organized, proactive, and eager to learn, to support analytical method validation activities, technical documentation, and quality control routines. Scope Support the execution of analyses related to analytical method validation, following internal procedures and regulatory requirements; Assist in drafting and organizing protocols, reports, and technical records; Support forced degradation studies and monitoring of analytical results; Contribute to method transfer and partial validation activities under technical guidance; Support analysis and organization of validation data, such as linearity, precision, accuracy, LOD, and LOQ; Operate analytical instruments including HPLC/UPLC, UV/Vis, dissolution testers, IR, and others, as trained and directed; Assist in deviation investigations, OOS/OOT evaluations, and preparation of technical justifications; Work in compliance with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), ANVISA regulations, and applicable ICH guidelines. Requirements Initial experience in quality control, analytical method validation, or laboratory routines; Bachelor’s degree completed or in progress in **Chemistry, Pharmacy, Chemical Engineering**, or related fields; Basic or intermediate knowledge of analytical techniques, especially HPLC/UPLC and dissolution testing; Fundamental understanding of analytical validation, technical documentation, and data integrity; Knowledge of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP); Basic or intermediate English proficiency for reading technical documents is considered a plus; Familiarity with software such as Lab Solutions and Empower is considered a plus; Ethical, organized, detail-oriented, proactive, and possessing strong interpersonal communication skills. Conditions **Individual Contractor — PJ** **Honorarium: R$ 4\.000,00** **Location:** Vargem Grande Paulista – SP **Work Model:** On-site **Start Date:** Immediate Why become a Kivalita partner? At Kivalita, you will have the opportunity to learn from experienced professionals, participate in impactful projects within the Life Science sector, and develop your career in a collaborative, technically rigorous, and continuously growing environment. If you seek an opportunity to grow, learn, and join a company that unites quality, technology, and purpose, become a **Kivalita Lion**! **Register\-yourself and good luck!**
João Silva
Indeed · HR
João Silva
Indeed · HR
