PpbJob Title: /b Process Engineer – Pharmaceutical Project /p pbContract Type: /b Freelance / Contract /p pbDuration: /b 5 months /p pbStart Date: /b ASAP /p h3Role Overview /h3 pWe are seeking an experienced Process Engineer to support a major pharmaceutical project in Visp, Switzerland. This is a hands‑on, multidisciplinary role requiring strong technical capability across process design, calculations, and engineering review. /p pThe successful candidate will play a key role in ensuring process systems are technically sound, compliant, and validated, supporting both engineering delivery and project execution. /p h3Key Responsibilities /h3 ul liDevelop and review process design documentation, including: /li liProcess Flow Diagrams (PFDs) /li liPiping Instrumentation Diagrams (PIDs) /li liPerform and validate process calculations, including: /li liFlow rates, mass and energy balances /li liEquipment sizing and performance verification /li liConduct plausibility checks on engineering deliverables and design assumptions /li liDefine and support User Requirement Specifications (URS) /li liSize and specify key process equipment, including: /li liPumps /li liVessels and tanks /li liProcess systems and utilities /li liInterface with multidisciplinary teams (mechanical, automation, electrical, validation) /li liSupport design reviews, HAZOPs, and project engineering activities /li liEnsure compliance with pharmaceutical and GMP standards /li liProvide technical input throughout design, construction, and commissioning phases /li /ul h3Requirements /h3 ul liProven experience as a Process Engineer within pharmaceutical or life sciences projects /li liStrong knowledge of: /li liProcess engineering fundamentals /li liEquipment sizing and system calculations /li liPharmaceutical production processes (API, sterile, or biotech preferred) /li liExperience producing or reviewing: /li liPFDs, PIDs /li liURS and engineering specifications /li liDemonstrated ability to perform plausibility checks and validate design outputs /li liExperience working in a multidisciplinary engineering environment /li liKnowledge of GMP regulations and compliance standards /li liStrong analytical and problem‑solving abilities /li /ul h3Language Location Requirements /h3 ul libGerman: /b Preferred (for site coordination and documentation) /li liWillingness to work on‑site in Visp, Switzerland /li /ul h3Why This Role /h3 ul liHigh‑profile pharmaceutical project in a leading European hub /li liLong‑term freelance contract with strong project pipeline /li liOpportunity to work within a multidisciplinary, international team /li liExposure to complex, high‑value engineering solutions /li /ul /p #J-18808-Ljbffr