Process Engineer
vor 2 Wochen
General Information Date : 02.02.2026 Latest Possible Start Date : 02.03.2026 Duration : until 30.09.2026 with the possibility of extension Workplace : Basel Workload : 100% Team : 20 team members Department : Pharma Engineering Drug Substance Working Hours Hours : Standard About the job The Pharma Engineering Drug Substance Small Molecules division ensures the technical support and further development of the production facilities for the manufacture of chemical active ingredients at the site in Basel. They work in self‑organized teams, focusing on proactive action, independent task management, and active teamwork. The role is initially vacant to temporarily strengthen the team and cover project peaks, with a clear possibility of long‑term employment if the collaboration is successful. Profile The ideal candidate holds a degree in process engineering or a related field and has more than five years of experience in a GMP environment. Tasks & Responsibilities Engineering & Technical Planning: Processing: Independent processing and maintenance of P&IDs in COMOS and ensuring data consistency. Design Documentation (DQ): Creation of technical specifications, data sheets, and technical drawings for execution. Isometrics: Technical review and approval of isometrics and manufacturing documents from pipeline construction companies. Project Management & Implementation (Construction): Trade Coordination: Management and coordination of the various trades (pipeline construction, instrumentation and control, automation, construction) for planning, execution, and commissioning. Construction Management: On‑site support of the implementation to ensure assembly quality and compliance with safety regulations. Resource Management: Ensuring that small projects are completed within the agreed scope, quality, budget, and deadlines. GMP Compliance, Qualification & Change Management: Change Control: Definition and establishment of all necessary measures (organizational, technical, documentation) for successful and compliant implementation of changes. Verification (IQ/OQ): Creation of acceptance documentation (test plans, protocols) for verifying installations and support during acceptance testing. Documentation: Compilation of the complete "as‑built" documentation and handover to the operator. Must Haves Completed technical or scientific degree (University of Applied Sciences / University / ETH) in Process Engineering, Chemical Engineering, Pharmaceutical Engineering or comparable field / completed advanced vocational training (Diploma Technician HF) with several years of relevant professional experience. At least 5 years of experience in a GMP environment; thorough familiarity with regulations and requirements of pharmaceutical production. Proficient use of standard PC applications; experience with SAP, myBuy, ELIVS / COMOS is a significant advantage. Excellent written and spoken German skills essential for documentation and communication within the company. Ability to work independently, proactively identify tasks, handle them transparently, and take responsibility. Cooperative team player with strong communication, sense of urgency, prioritisation, and ability to write precise technical texts. Nice to have Excellent written and spoken English skills. Experience using Google Suite and openness to AI applications for process support. Application Submission Deadline: 15.12.2025 #J-18808-Ljbffr
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