QC Specialist

Perform bioanalytical release and stability testing in compliance with cGxP and data integrity requirements. Prepare, evaluate, and report on project-related protocols, plans, trend analyses, and testing activities. Implement new product testing into the routine laboratory and support method development and validation activities. Manage analytical weak points, perform complex troubleshooting, and support continuous improvement of laboratory workflows. Review analytical data and tests, including analytical release activities, to ensure accuracy, quality, and compliance. Handle OOx results and deviations, define CAPAs, and contribute to effective investigation processes. Maintain and calibrate laboratory equipment, including preparation of maintenance and calibration plans. Act as SPoC or SME for bioanalytics initiatives and contribute to relevant documentation workflows and technical authoring. Support sample planning, sampling execution, supplier qualification, and KPI/KQI trending and analysis. Follow all HSE guidelines, proactively identify and report potential risks, propose solutions, and participate in required trainings.

This role is based in Basel, Switzerland. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. Join our team as a QC Specialist and play a key role in ensuring high-quality, compliant laboratory operations. Working in a GxP-regulated environment, you will help ensure that laboratory activities are performed in line with GxP and HSE guidelines, while reviewing and approving analytical data to maintain accuracy, reliability, and compliance. This is an excellent opportunity for a detail-oriented scientific professional who enjoys combining hands-on technical knowledge with quality-focused decision-making.

• Technical education with 3–5 years of relevant experience, or a university degree in Pharmacy, Chemistry, or equivalent with 0–4 years of working experience.

• Professional experience in the pharmaceutical sector, active substance manufacturing, or analytical laboratories within a GMP environment or equivalent.

• Good understanding of Quality Control testing, QC sampling, laboratory excellence, and related GxP standards and processes.

• Experience working with laboratory equipment and supporting analytical or quality-related laboratory activities.

• Strong collaboration skills with the ability to communicate effectively across teams, departments, and functions.

• Result-oriented mindset with strong analytical thinking, resilience, and a focus on operational excellence.

• Commitment to continuous learning and the ability to adapt to digital tools, technologies, and evolving processes.

• Good knowledge of MS Office and standard IT applications supporting quality activities.

• Sound quality decision-making skills and understanding of industry quality standards.

• Good written and spoken English skills and fluency in German (a plus).