Commissioning & Qualification Engineer (Oral Solid Dosage) – available at short notice – 100% on-site Pharma Industry (Ref. 2820) - 6 months temporary contract - E/F

pOur client is a leading pharmaceutical company with a state-of-the-art production site in the Neuchâtel area, operating globally and ranking among the largest employers in the industry in Switzerland. To support capital projects within a GMP-regulated manufacturing environment, we are looking for an experienced professional as /ph3Commissioning Qualification Engineer (Oral Solid Dosage) – French English speaking – available at short notice – 100% on-site Pharma Industry (Ref. 2820) - 6 months temporary contract – Neuchâtel Area /h3pIn this project-focused role, you will lead and coordinate commissioning and qualification activities for facilities, utilities, manufacturing equipment, automation, and computerized systems. You will work closely with Engineering, Technical Services, Manufacturing Science and Technology, Quality Assurance, end users, suppliers, and external contractors to ensure successful project delivery. The position combines technical leadership, contractor coordination, project scheduling, and hands-on qualification expertise /pulliOversee commissioning and qualification activities for capital projects, ensuring completion within agreed timelines and budgets. /liliLead and coordinate colleagues and external contractors responsible for qualifying facilities, utilities, oral solid dosage equipment, and computerized systems. /liliDevelop CQ strategies, plans, schedules, acceptance criteria, protocols, and final reports. /liliCoordinate the execution, review, approval, and completion of qualification deliverables according to project milestones. /liliCollaborate with internal departments, suppliers, engineering partners, construction teams, and validation contractors to achieve project objectives. /liliSupport investigations, change controls, impact assessments, and corrective action plans related to commissioning and qualification activities. /liliAct as a subject-matter expert during internal and external audits and provide the required qualification and validation documentation /li /ulh3Your profile /h3ullibDegree in Engineering, Life Sciences, Mechanical Engineering, Chemical Engineering /b, or another relevant technical or scientific discipline. /lilibApproximately 3-5 years of relevant experience in the pharmaceutical industry /b, involving boral solid dosage /b bvalidation /b in a GMP environment. /lilibProven experience managing /b bcomplex CQ projects /b, external contractors, project resources, and multidisciplinary teams. /lilibStrong knowledge of /b equipment, utilities, automation, computerized system validation, and pharmaceutical qualification requirements. /lilibExperience with project management /b, change management, investigations, and product lifecycle activities. /lilibPrevious involvement in health authority inspections /b, including preparation, presentations, documentation, and responses to audit questions. /liliExcellent English and French skills are required. /li /ulpFull discretion is guaranteed and we will gladly answer any additional questions. /p #J-18808-Ljbffr