Stellenbeschreibungph3Commissioning, Qualification Validation Professionals – Switzerland /h3 pCompany: Kinetics Process Consulting GmbH /p pLocation: Switzerland – Basel, Visp, and other major pharmaceutical manufacturing hubs /p pEmployment Type: Permanent /p pWe are expanding our presence in Switzerland and are interested in speaking with experienced Commissioning, Qualification and Validation professionals for current and upcoming pharmaceutical and biopharmaceutical projects. We support major capital projects from strategy and design through commissioning, qualification, start‑up and operational readiness. Opportunities may be available across both project leadership and hands‑on execution roles. /p h3Areas of Interest /h3 ul liCommissioning and Qualification leadership /li liClean and black utilities /li liHVAC and cleanrooms /li liDrug substance and drug product manufacturing /li liFill‑finish and aseptic processing /li liBuffer and media preparation /li liCIP and SIP systems /li liUpstream and downstream process equipment /li liLaboratory and analytical equipment /li liAutomation and Computer System Validation /li liThermal mapping /li liQualification documentation and document generation /li liQuality Assurance and validation oversight /li liKNEAT, Veeva or other electronic validation systems /li /ul h3Typical Responsibilities /h3 ul liDeveloping and implementing commissioning and qualification strategies /li liPreparing, reviewing and executing lifecycle documentation /li liSupporting DQ, FAT, SAT, commissioning, IQ, OQ and PQ activities /li liReviewing URS, specifications, risk assessments and traceability matrices /li liManaging deviations, punch items and qualification close‑out /li liCoordinating with engineering, quality, automation, vendors and operations teams /li liProviding technical leadership across assigned systems or workstreams /li liSupporting inspection readiness and compliance with applicable GMP requirements /li /ul h3Candidate Profile /h3 ul liExperience within pharmaceutical, biotechnology or other regulated manufacturing environments /li liPractical commissioning, qualification or validation experience /li liA strong understanding of GMP requirements and the project lifecycle /li liThe ability to work effectively with multidisciplinary and international teams /li liStrong technical documentation and communication skills /li liProfessional fluency in English; German or French language skills and familiarity with Swiss pharmaceutical sites would be advantageous, but are not essential for every position /li /ul h3Work Eligibility /h3 pApplications are welcome from candidates already authorized to work in Switzerland, EU/EFTA nationals and other experienced professionals who may require work‑permit support. Any potential work‑permit or relocation requirements will be reviewed individually and will depend on the position, project location, candidate experience and applicable Swiss immigration requirements. /p h3About KPC International /h3 pKPC International has supported pharmaceutical and biopharmaceutical projects worldwide since 2001. Our teams provide specialist engineering, commissioning, qualification, validation and project delivery services from concept through start‑up and operation. We offer the opportunity to work on technically challenging projects with leading life‑sciences organisations, supported by an experienced international team. /p pBy email: /p /p #J-18808-Ljbffr