We are a Brazilian pharmaceutical company that has been dedicated to life for over 65 years. Driven by the purpose of "transforming knowledge into health for your life," we have built our history with boldness, innovation, and a visionary spirit. **Our reason for being** is to promote high-quality healthcare so people can enjoy every moment. We offer a broad portfolio of medications across various specialties such as gynecology, oncology, and cardiology, addressing patients holistically and individually with efficient and innovative formulations. We have over 100 brands in more than 200 presentations. **We want you to find your place here!** We are recognized as an excellent workplace according to GPTW. 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. **\#BecauseLifeDeservesCare** **Responsibilities and duties** **On a daily basis, you will:** * Provide technical support to various company departments regarding processes, formulations, technical manufacturing conditions, deviations, and/or non-conformities, ensuring deadlines are met and problems resolved. * Propose formulations for improvements/optimizations of existing medicines through scientific evidence and evaluation of reference or proposed comparator medicines. * Identify opportunities for continuous improvement in production processes by analyzing ways to optimize manufacturing, interacting with other departments to evaluate and implement process enhancements. * Transfer generated technology and knowledge to the production and client departments by executing pilot batches and monitoring industrial product batches. * Evaluate stability study results from ongoing projects to identify out-of-specification outcomes and propose solutions to ensure adequate product stability. * Provide technical documentation related to manufacturing processes and formulations to the technical documentation team to support the preparation of dossiers submitted to regulatory agencies for process approval, as well as assist in reviewing technical documents for post-registration and registration renewal purposes. * Support company departments in responding to requirements issued by ANVISA by providing technical information and performing additional tests to prepare technical justifications. * Support the process validation team by providing detailed process, formulation, and manufacturing technique information, assisting in product risk assessments, validation protocol development, and equipment qualification. * Identify medicine-related issues by conducting investigations and clarifying possible technical questions to support Quality Assurance, Medical Information, Customer Service, and Marketing\-Product Managers with materials and tests for customer responses and training. **Requirements and qualifications** **To participate in our process:** * Completed bachelor's degree in Pharmacy. * Experience in formulation development or improvement departments, focusing on line products and post-registration activities. * Pharmaceutical technology knowledge in manufacturing techniques such as fluid bed granulation/coating, high-shear mixer granulation, multiparticulate coating, tablet coating, capsule filling, and powder packaging. * Pharmaceutical technology knowledge in manufacturing liquids, semisolids, injectables (solutions and lyophilized). * Problem-solving skills with a focus on continuous improvement of products and processes. * Knowledge of QbD concepts and critical assessment for risk management throughout the product lifecycle. * Familiarity with current national and international regulations. * English proficiency for reading and writing; intermediate conversational level for business travel and international calls. **You will stand out if you have:** * Knowledge of statistical tools and experimental design. * Knowledge of problem-solving tools. * Knowledge of biologics. **Additional information** **\+ Information** Work location (Base): Embu das Artes SP Working hours: Flexible administrative schedule **Benefits for you!** * Meal allowance; * Food allowance; * Libbs Medications \- 100%; * Pharmacy network – Vidalink; * PPR \- Profit and Results Participation Program; * Parking, transportation allowance, or shuttle service (applicable only for shift work); * Flexible benefits (life insurance, private pension, medical, dental, and food assistance). We are a Brazilian pharmaceutical company that has been dedicated to life for over 67 years. Driven by the purpose of "transforming knowledge into health," we have built our history with boldness, innovation, and a visionary spirit. Here, we believe that **diversity** strengthens our purpose and relationships. All positions are evaluated with inclusion in mind, based on competence assessment. **Our reason for being** is to promote high-quality healthcare so people can enjoy every moment. We offer a broad portfolio of medications across various specialties such as gynecology, oncology, and cardiology, addressing patients holistically and individually with efficient and innovative formulations. We have over 100 brands in more than 240 presentations. **We want you to find your place here!** We are recognized as an excellent workplace according to GPTW. 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 have a manufacturing unit in Embu das Artes, logistics centers in Embu and Varginha, and our administrative team working 100% remotely with access to coworking spaces worldwide.