Technician Drug Supply

Job ID REQ-10084109 Jul 23, 2026 Switzerland Available in: German Summary ### Location: Basel, Switzerland \#onsite Role Objective: We are looking for a Chemical and Pharmaceutical Technician (CPT) to support the Chemical & Analytical Development (CHAD) department within Global Technical R&D (TRD). In this role, you will manufacture intermediates and Drug Substances (DS) for clinical supply in early and late development phases. Manufacturing is carried out according to approved manufacturing instructions, SOPs, GMP, and HSE requirements, as well as applying established contamination control and cleanroom working methods. The product spectrum includes various modalities such as synthetic oligonucleotides, peptides, classic organic active ingredients, and DS bioconjugates. Depending on the process, you will work in classified production areas up to Zone A, e.g., during open or particularly contamination-critical process steps for low-bioburden DS/bioconjugates. We offer you a dynamic, agile environment with varied projects, high individual responsibility, and development opportunities. About the Role ### Your responsibilities include the GMP-compliant, safe, and efficient execution of manufacturing processes as well as the active support of a robust production operation: • Preparation, setup, and process-related provision of plants, equipment, materials, consumables, and production documentation. • Independent operation of complex process plants, systems, and process-specific special equipment according to PMPs, SOPs, and batch strategy. • Execution of manufacturing steps for intermediates and DS, including low-bioburden and bioconjugate processes, in compliance with defined GMP, GSU, HSE, and cleanroom requirements. • Working in classified production areas up to Zone A, including correct gowning, aseptic-oriented working methods, material transfer, disinfection, line clearance, and avoidance of microbial as well as particulate contamination. • Ensuring a disciplined way of working during open product handling, especially during contamination-critical process steps such as dispensation, filtration, filling/aliquoting, or other bioconjugate-relevant activities. • Execution and documentation of in-process controls, process observations, and other production-accompanying controls according to specifications. • Complete, timely, and GMP-compliant documentation of all relevant information in the batch record and in the associated systems. • Dismantling, cleaning, disinfection, reassembly, and preparation for release of process plants, equipment, and work areas after production. • Execution of waste disposal activities according to internal and external specifications, including exhaust air, wastewater, liquid, and solid waste concepts. • Active contribution to order, cleanliness, 5S, sustainable maintenance, and safe operation of the production areas. • Early detection, reporting, and support in the processing of plant, process, documentation, or compliance deviations. • Contribution of improvement and solution suggestions to optimize processes, safety, quality, cleaning procedures, and plant availability. • Cooperation with Process Chemists, team coordination, QA, Engineering, HSE, Planning, Warehouse, and other internal stakeholders for timely and quality-compliant project execution. • Support and technical guidance of less experienced employees in plant operation, GMP documentation, cleanroom behavior, process execution, and cleaning. • Assumption of defined special tasks according to responsibility lists, e.g., in the areas of process controls, training, shift support, plant responsibility, or continuous improvement.   What you bring: • Completed training in a technical, chemical, pharmaceutical, or related field (e.g., laboratory); ideally as a Chemical and Pharmaceutical Technician EFZ. • Practical experience in chemical or pharmaceutical manufacturing, preferably in GMP-regulated production facilities. • Good knowledge in handling computer-aided control systems as well as understanding of GMP, GSU, HSE, and documentation requirements. • Experience or willingness to qualify for cleanroom activities, including working in classified areas up to Zone A and applying low-contamination or aseptic-oriented working methods. • Understanding of pharmaceutical manufacturing processes for DS, ideally with reference to low-bioburden processes, bioconjugates, filtration, dispensation, filling/aliquoting processes, or single-use systems. • Willingness to work in a 3-shift model and for extended periods in cleanroom clothing or full protective suits, including supplied-air systems. • Careful, reliable, and quality-conscious way of working with a high sense of responsibility for patient safety, product protection, and compliance. • Very good German skills in speaking and writing as well as basic knowledge of English. Vantages & Rewards At Novartis, we are committed to rethinking medicine together - and rewarding the people who make it possible.   Expected annual basic salary range for the role: -56,840 to -105,560   The offered basic salary is determined based on gender-neutral goals such as relevant skills, competencies, and experience in accordance with the Novartis salary policy and is regularly reviewed at Novartis.   In addition to your basic salary, you may be eligible for a performance-based bonus depending on certain performance parameters.   The rewards of being part of our team go far beyond basic salary and incentives. We also offer a variety of competitive benefits so that you can succeed both personally and professionally s