**Job Summary** The Production Analyst is responsible for supporting, planning, monitoring, and optimizing the manufacturing processes of pharmaceuticals and pharmaceutical products, ensuring compliance with regulatory standards (ANVISA, RDCs, Good Manufacturing Practices – GMP), operational efficiency, product quality, and operational safety. Also responsible for administrative tasks relevant to the Production area. **Responsibilities and Duties** · Monitor and control production process stages and their respective cycle times, ensuring compliance with standard operating procedures (SOPs) and GMP regulations, and proposing improvements whenever applicable using tools such as SMED, PDCA, etc.; · Develop, review, plan, and execute production orders, master production records, and batch records; · Perform material reconciliation, consumption control, and yield tracking; · Monitor performance indicators (OEE, productivity, waste, deviations); · Support deviation and non-conformance investigations, contributing to the definition of corrective and preventive actions (CAPA); · Participate in process validations, equipment qualification, and continuous improvement initiatives; · Ensure production routines are executed in accordance with quality, safety, and environmental policies; · Train operators on procedures, process changes, and good practices; · Interact with departments such as Quality Assurance, Maintenance, Procurement, Logistics, and Technical Area as needed; · Monitor testing of new equipment, scale-up activities, and technology transfer; · Assist in managing technical documentation (SOPs, work instructions, reports, forms); · Support internal and external audits (ANVISA, FDA, certifications); · Manage the entire procurement process for the Production area—from requesting quotations, placing purchase orders, receiving goods, to entering invoices into the system for payment. **Education** Bachelor’s degree in Pharmacy, Chemical Engineering, Production Engineering, Chemistry, or related fields. **Technical Knowledge** * GMP and regulatory standards (RDCs); * Manufacturing processes: solids, liquids, semi-solids, injectables; * Continuous improvement tools (Lean, Kaizen, 5S, Six Sigma – desirable); * Interpretation of operational data and deviation investigation; * ERP/MES systems (e.g., SAP, Totvs); * Microsoft Office suite, especially Excel. **Behavioral Competencies** * Attention to detail and quality focus; * Analytical ability and problem-solving skills; * Teamwork and effective communication; * Organization, discipline, and sense of responsibility; * Data-driven decision making. **Desired Experience** * Prior experience in pharmaceutical, cosmetic, chemical, or regulated consumer goods environments; * Hands-on experience with routine manufacturing processes and production documentation. **Working Conditions** * Industrial environment requiring uniform and personal protective equipment (PPE); * Availability to work rotating shifts; * Frequent interaction with multidisciplinary teams. **Benefits** * Salary advance * Medical assistance * Dental assistance * Food allowance * Meal voucher * Gympass (Wellhub) * Career development plan Employment type: Permanent CLT contract Compensation: R$5.000,00 – R$7.000,00 per month Selection question(s): * Do you have basic knowledge of sanitary legislation and Good Manufacturing/Handling Practices (GMP/GHP)? * Do you possess the ability to read and interpret technical specifications for raw materials and inputs?