Process Engineer PAR NPI/LCM

The role of a Process Engineer PAR NPI/LCM at Johnson & Johnson involves working in the pharmaceutical industry, specifically focusing on the introduction of new products into commercial production and the implementation of new technologies and processes. Johnson & Johnson is a global healthcare company known for its innovative medicines and medical technologies, aiming to prevent, treat, and cure complex diseases. The main day-to-day responsibilities include acting as a core team member in technology transfer projects for new product commercialization. This involves preparing and executing engineering runs, clinical batches, and validation batches in collaboration with various teams. The role also entails leading and supporting improvement projects to enhance process robustness, compliance, and operational performance. Additionally, the engineer will manage change controls, recipes, and document updates, and train teams on project-related content and process changes. They will also serve as a subject matter expert during audits and inspections, ensuring compliance with GMP, EHS, and SOX guidelines. To qualify for this role, candidates must have a Bachelor's degree in natural sciences or engineering, with a Master's degree being preferred. At least 4 years of experience in the pharmaceutical industry, including 2 years in parenteral or pharmaceutical manufacturing or development, is required. Knowledge of late-stage development activities and manufacturing site unit operations, such as compounding, milling, and filling of liquid formulations and suspensions, is essential. Strong planning and logistics skills, as well as proficiency in German and English, are also required. Experience with manufacturing site systems like SAP, PAS-X, or equivalent systems is necessary. Nice-to-have skills include experience with Agile Manufacturing, Analytics Dashboards, and Business Behavior. Knowledge in Chemistry, Manufacturing, and Control (CMC), as well as Competitive Landscape Analysis, Data Compilation, and Data Savvy, would be beneficial. The role is based in Schaffhausen, Switzerland, and offers an inclusive work environment where diversity and individual merit are respected. The company is committed to providing an interview process that accommodates the needs of all applicants. What the role asks for: - Bachelor's degree in natural sciences or engineering - 4+ years of experience in the pharmaceutical industry - 2+ years of experience in parenteral or pharmaceutical manufacturing or development - Proficiency in German and English - Knowledge of late-stage development activities and manufacturing site unit operations - Knowledge of manufacturing site systems, such as SAP, PAS-X, or equivalent systems - Strong planning and logistics skills - Nice-to-have: Experience with Agile Manufacturing