Job Summary: We are seeking a professional to ensure the quality of pharmaceutical products in Riells, performing physicochemical analyses and collaborating in quality management. Key Responsibilities: 1. Ensure pharmaceutical quality at the production plant 2. Perform physicochemical analysis of semi-finished products 3. Collaborate in laboratory verification and maintenance **Location:** Riells I Viabrea * *Ensure that pharmaceutical products manufactured in Riells comply with Good Manufacturing Practices (GMPs) and Sanofi directives* * *Actively participate across all areas to implement management practices enabling the Riells production plant to achieve Group objectives regarding: QUALITY STANDARD, SAFETY STANDARD, COST STANDARD, SERVICE STANDARD, BUDGET COMPLIANCE* * *Comply with applicable regulations (external or internal) concerning labor legislation, quality protocols, environmental protection, and occupational safety.* * *Actively participate in talent management initiatives promoted by the company.* * *Comply with HSE policy, procedures, and instructions.* * *Use work equipment and tools correctly.* * *Use provided PPE in defined situations, maintain them in good condition, and request replacement when damaged or expired.* * *Report hazardous situations or any incidents to the HSE team.* * *Comply with applicable Quality regulations relevant to the performance of duties.* * *Perform physicochemical analysis of semi-finished products and stability samples (ICH and on-going)* * *Receive semi-finished product samples* * *Ensure availability of consumables and reagents under appropriate conditions* * *Collaborate in verification, qualification, and maintenance of laboratory facilities and equipment* * *Other duties assigned within the Quality area* ***Requirements:*** * *Technical education in Pharmaceutical Analysis and Control,* * *Minimum one year of experience using analytical techniques such as HPLC, UV, and Gas Chromatography, plus experience in pharmaceutical analysis and control.* * *In-depth knowledge of GMP regulations is mandatory,* * *Familiarity with LIMS and Empower systems will be considered an advantage,* * *We seek a methodical, rigorous individual with strong organizational skills, ability to multitask efficiently, agility, and accustomed to teamwork.* null