Job Summary: Professional responsible for ensuring the quality of processes, products, and services through physicochemical analyses and indicator monitoring. Key Highlights: 1. Leadership in sterile drug compounding 2. Guarantee of excellence and continuous process improvement 3. A team of champions focused on hard-to-access medications **About the Company** **If you are an energetic, determined professional who loves challenges, join Pharmédice—the leader in sterile drug compounding.** Founded in Minas Gerais, Pharmédice Manipulações Especializadas redefines excellence in sterile drug compounding for human health. Pharmédice not only meets the industry’s highest compounding standards but elevates them to a new level. We combine regulatory rigor, intelligent use of data, and unparalleled expertise to deliver sterile drugs with speed and quality. A team of champions embodying excellence in its DNA—a team composed of pharmacists specialized in various fields, technicians, specialists, engineers, analysts, supervisors, IT professionals, commercial staff, logistics personnel, and procurement specialists. All united by one shared purpose: **ensuring market access to hard-to-access medications.** **So, if you believe you are an exceptional professional ready to make a difference in our structure and national growth, join us!** **Job Description** Collaborate to ensure that the organization’s processes, products, and services comply with quality requirements established by internal standards, applicable legislation, and current certifications; manage documentation control and monitor indicators, thereby ensuring compliance and continuous process improvement. **Responsibilities and Duties** * Physicochemical analyses of raw materials, finished products, and packaging materials; * Water analysis; * Preparation of reagent solutions and analytical standards; * Sampling of raw materials and packaging materials; * Recording, evaluating, and reporting analytical results; * Assisting in investigations of deviations, out-of-specification (OOS) results, and nonconformities. **Requirements and Qualifications** **Education:** Technical degree (pharmacy, chemistry, biotechnology, or related fields). Pursuing a bachelor’s degree—up to sixth semester preferred. Solid experience with HPLC. **Experience:** Prior experience in Quality Assurance, preferably within industrial or pharmaceutical companies. **Technical Knowledge:** * Quality Management Systems (ISO 9001, GMP, HACCP, or equivalents) * Quality tools (5W2H, PDCA, Ishikawa, MASP, Pareto, etc.) * Document control and audits * Interpretation of applicable standards and legislation * Microsoft Office (intermediate to advanced level) * Mandatory HPLC equipment experience—data evaluation and processing using Empower software (Waters) **Benefits** * Meal Allowance: BRL 23.00/day * Transportation Allowance / Fuel Allowance * UsiSaúde Health Plan (no monthly fee—only co-payment) * Dental Plan: BRL 26.00/month (optional) * Working hours: 08:00–17:48, Monday to Friday * SESC and Pharmacy Partnerships Employment Type: Full-time CLT Working Hours: Monday to Friday, 08:00–17:48 Employment Type: Full-time **Required Experience:** * HPLC equipment operation (Mandatory) * Minimum 3 years’ experience in a compounding laboratory (Mandatory) Employment Type: Full-time, Full-time CLT Compensation: BRL 2,594.00 – BRL 2,600.00 per month Work Location: On-site