Junior Commissioning Engineer

pInova is a Swiss consulting and engineering firm specializing in supporting life sciences industries through high-value expertise in engineering, commissioning qualification, quality, compliance, and digital transformation. We support our clients throughout the lifecycle of pharmaceutical facilities and critical systems, from design and project execution through commissioning, qualification, and operational readiness. /p h3Position Overview /h3 pWe are seeking a motivated Junior Commissioning Engineer to support a pharmaceutical project in the Basel area but bthe role requires 100% travel /b, with a focus on isolators, clean rooms, and associated HVAC systems. /p pIn this role, you will contribute to commissioning and qualification activities on critical GMP equipment and facilities, with a particular emphasis on IQ and OQ execution for isolators and air handling systems, including smoke studies, alarm verification, and functional testing. /p pThis is a highly operational, hands‑on role. You will spend the majority of your time on site, directly on the equipment: performing calibration of isolators and associated instrumentation, executing tests in the field, and troubleshooting with suppliers and technicians. This is not a desk‑based documentation position. /p h3The role requires 100% travel. /h3 pYou will be permanently assigned to client sites across Europe, with no fixed office base. /p pYou will work closely with Engineering, QA, Operations, Automation, and equipment suppliers to ensure that systems are properly commissioned, qualified, and documented in compliance with GMP requirements and project specifications. /p pThe position is ideal for an engineer with first CQV experience who wants to develop strong hands‑on expertise in a demanding project environment, as part of a collaborative team. /p h3Key Responsibilities /h3 ul liPerform bhands‑on calibration of isolators and associated instrumentation /b (pressure, temperature, humidity, airflow sensors), including verification of calibration status and documentation /li libCarry out field execution work directly on equipment: /b installation checks, functional testing, leak testing, and glove integrity testing /li libWork full time on site /balongside suppliers, technicians, and operations teams during commissioning and qualification phases /li liSupport the planning and execution of commissioning and qualification activities for isolators, clean rooms, and air handling systems /li libExecute IQ and OQ protocols, including installation verification, functional testing, and alarm and interlock verification /b /li liParticipate in airflow visualization (smoke studies), pressure cascade verification, and clean room classification activities /li liReview functional specifications, bPIDs /b, and vendor documentation against user requirements /li liDraft and review GMP documentation, including test scripts, protocols, deviation reports, and final qualification reports /li liVerify installation and functionality of equipment, instrumentation, HVAC components, alarms, and control systems /li liDocument test results accurately and ensure traceability between user requirements, risk assessments, and qualification testing /li liManage punch‑list items, discrepancies, and deviations through resolution, with support from senior CQV engineers /li liCollaborate closely with Engineering, QA, Automation, Operations, and Validation teams /li liEnsure CQV activities comply with applicable GMP requirements, EU GMP Annex 1 and Annex 15, ISPE guidance, and internal quality procedures /li liSupport system handover and transition from project execution into routine GMP operation /li /ul h3Profile Requirements /h3 ul liDegree in Chemical Engineering, Mechanical Engineering, Process Engineering, Biotechnology, Pharmaceutical Engineering, or a related technical discipline /li li1 to 3 years of experience in Commissioning, Qualification Validation (CQV) within the pharmaceutical, biotech, or life sciences industry, including internships or first project assignments /li liFirst hands‑on experience with isolators and clean rooms, ideally including air handling systems and smoke studies /li liPractical experience executing IQ and OQ, including alarm verification and functional testing /li liHands‑on, field‑oriented mindset with a genuine interest in working directly on equipment, including calibration activities /li liGood understanding of GMP documentation practices and ability to write clear, structured, and compliant documents /li liBasic knowledge of GMP, EU GMP Annex 1 and Annex 15, and risk‑based qualification principles /li liAbility to read functional specifications, PIDs, and engineering drawings /li liStructured, curious, and quality‑focused working style /li liGreat soft skills: strong communication, genuine team player, and comfortable interacting with multidisciplinary teams, vendors, and clients /li liExcellent English, written and spoken /li lib100% travel required: full mobility within Europe and willingness to be based on client sites for the full duration of project assignments /b /li /ul h3Why Join Inova? /h3 ul liWork on major pharmaceutical engineering and CQV projects in the Basel life sciences ecosystem /li liBuild hands‑on expertise on isolators, clean rooms, and HVAC qualification alongside experienced CQV engineers /li liA genuinely field‑based role where you build technical credibility through hands‑on execution, not just documentation /li liBenefit from mentoring and a clear development path within our CQV practice /li liCollaborate with experienced Engineering, CQV, QA, and Automation specialists /li liJoin a dynamic Swiss company that values technical excellence, autonomy, precision, and collaboration /li /ul pInova is an equal opportunity employer. We welcome diverse perspectives and are committed to fostering an inclusive workplace. /p #J-18808-Ljbffr