




Job Summary: A professional to support quality assurance, ensuring compliance and continuous improvement of Pharmédice’s processes — a leader in sterile drug compounding. Key Highlights: 1. Work for a leading company in sterile drug compounding. 2. A team of champions with excellence embedded in its DNA and a focus on access to medications. 3. A top-tier professional ready to make a difference in national growth. **About the Company** **If you are an energetic, determined professional who loves challenges, join Pharmédice — a 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 unmatched expertise to deliver sterile medications rapidly and with exceptional quality. A team of champions carrying excellence in their DNA — composed of pharmacists specialized in various fields, technicians, specialists, engineers, analysts, supervisors, IT professionals, commercial staff, logistics and procurement personnel. All united by a single purpose: **ensuring market access to hard-to-obtain medications.** **So, if you believe you are a top-tier professional ready to make a difference in our structure and national growth, join us!** **Job Description** Support the organization’s processes, products, and services in meeting quality requirements established by internal standards, applicable legislation, and current certifications; manage documentation control and monitor key performance indicators, 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 deviation investigations, Out-of-Specification (OOS) results, and nonconformities. **Requirements and Qualifications** **Education:** Technical-level qualification (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 in 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 Suite (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 Agreements Employment Type: Permanent CLT Working Hours: Monday to Friday, 08:00–17:48 Employment Type: Full-time **Required Experience:** * Operation of HPLC equipment (Mandatory) * Minimum 3 years in a compounding laboratory (Mandatory) Employment Type: Full-time, Permanent CLT Salary: BRL 2,594.00 – BRL 2,600.00 per month Work Location: On-site


