QC Analyst II

The role of QC Analyst II at Novartis involves supporting Good 'x' Practice (GxP) activities within the quality department. The company is a global leader in pharmaceuticals, dedicated to developing innovative medicines and treatments. The position is crucial for maintaining quality standards and ensuring compliance with regulatory requirements. The main day-to-day responsibilities include maintaining compliance with Standard Operating Procedures (SOPs) and GxP-compliant documentation. The role also involves performing and evaluating analytical tasks in a pharmaceutical laboratory, which may require working in shifts. Additionally, the QC Analyst II ensures the integrity of quality assurance records and data, fosters collaboration between teams, and supports quality audits and health authority inspections. To qualify for this role, candidates must have experience in quality assurance and analytical skills. Proficiency in analytical technologies such as HPLC, GC, and titration is essential. Knowledge of lab-specific software like Empower, Chromeleon, and TiAmo is also required. Candidates must have GMP experience and technological expertise. Fluency in German and good English skills are mandatory. The role requires a willingness to work in shifts. Nice-to-have skills include a strong commitment to diversity and inclusion, as Novartis values an inclusive work environment. The role is based in Basel, Switzerland, and offers a collaborative team environment. The position is full-time and limited to 24 months. What the role asks for: - Experience in quality assurance and analytical skills. - Proficiency in analytical technologies (e.g., HPLC, GC, titration). - Knowledge in the use of lab-specific software (e.g., Empower, Chromeleon, TiAmo). - GMP experience and technological expertise. - Willingness to work in shifts. - Fluency in German and good English.