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Expert Engineering (Automation… at Novartis · Mengeš
ExperiencedOn-siteFull-timeMengeš, Mengeš, Slovenia
Job Description
Expert Engineering (Automation Engineer)/Inženir avtomatizacije
Location: Mengeš
Job Description Summary
Location: Menges, Slovenia #onsite
Klinična proizvodnja | Inženiring in avtomatizacija
Soustvarjajte prihodnost bioloških zdravil
V Novartisu soustvarjamo prihodnost zgodnje faze razvoja bioloških zdravil. V okviru te poti se BioCampus Mengeš razvija v najsodobnejši, integriran klinični proizvodni obrat za učinkovino (Drug Substance) in končni izdelek (Drug Product).
Za podporo tej rasti iščemo izkušenega inženirja avtomatizacije, ki želi imeti dejanski vpliv v visoko avtomatiziranem, GMP‑reguliranem okolju.
Vaša vloga
Kot inženir avtomatizacije boste ključni tehnični strokovnjak, odgovoren za avtomatizirane sisteme v proizvodnji in podpornih sistemih. Tesno boste sodelovali z oddelki inženiringa, proizvodnje, zagotavljanja kakovosti (QA), IT/OT ter zunanjimi partnerji, pri čemer boste prispevali tako k tekočemu obratovanju kot tudi k zanimivim novim projektom.
To delovno mesto je primerno za posameznika, ki uživa v samostojnosti, tehnični poglobljenosti ter delu na stičišču tehnologije, GMP skladnosti in proizvodne učinkovitosti.
Clinical Manufacturing | Engineering & Automation
Be part of building the future of biologics
At Novartis, we are shaping the future of early‑stage biologics. As part of this journey, BioCampus Mengeš is being developed into a state‑of‑the‑art integrated clinical manufacturing facility for Drug Substance and Drug Product.
To support this growth, we are looking for an experienced Automation Engineer (Expert) who wants to make a real impact in a highly automated, GMP‑regulated environment.
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Your role
As an Automation Engineer, you will be a key technical expert responsible for automation systems across manufacturing and supporting utilities. You will work closely with engineering, production, QA, IT/OT and external partners, contributing to both ongoing operations and exciting new projects.
This role suits someone who enjoys ownership, technical depth, and working at the interface between technology, GMP compliance and manufacturing performance.
Job Description
Ključne odgovornosti
Načrtovanje, implementacija in vzdrževanje avtomatizacijskih rešitev (PLC, SCADA, DCS, Historian, PIS) v GMP kliničnem proizvodnem okolju
Delovanje kot tehnični lastnik avtomatizacijskih sistemov skozi celoten življenjski cikel
Sodelovanje pri investicijskih projektih in nadgradnjah: URS, FS/DS, FAT/SAT, IQ/OQ ter predaja sistemov v uporabo
Zagotavljanje skladnosti z GMP, GxP, načeli integritete podatkov ter internimi standardi Novartisa
Upravljanje sprememb na avtomatizacijskih sistemih preko postopkov Change Control
Podpora proizvodnji z odpravljanjem zahtevnih avtomatizacijskih težav in optimizacijo delovanja sistemov
Sodelovanje z IT/OT oddelkom in dobavitelji za zagotavljanje razpoložljivosti sistemov, kibernetske varnosti in dolgoročne vzdržnosti
Podpora pri notranjih in zunanjih revizijah ter inšpekcijah
Mentorstvo ter tehnična podpora mlajšim inženirjem v ekipi
Vaš profil
Univerzitetna izobrazba s področja avtomatizacije, elektrotehnike, mehatronike, računalništva ali sorodnih smeri
Vsaj 5 let ustreznih delovnih izkušenj, od tega najmanj 2 leti v GMP‑reguliranem okolju (farmacija, biotehnologija ali kemijska industrija)
Močne praktične izkušnje s sistemi PLC / SCADA / DCS ter industrijskimi omrežji
Izkušnje z validacijo računalniških sistemov (CSV) in regulirano dokumentacijo
Sposobnost samostojnega dela, sprejemanja utemeljenih tehničnih odločitev ter jasnega komuniciranja z različnimi deležniki
Role: Expert Engineering (Automation Engineer)
Be part of building the future of biologics
Design, implement and maintain automation solutions (PLC, SCADA, DCS, Historian, PIS) in a GMP clinical manufacturing environment
Act as technical owner of automation systems across their full lifecycle
Participate in capital projects and upgrades: URS, FS/DS, FAT/SAT, IQ/OQ and system handover
Ensure compliance with GMP, GxP, Data Integrity and Novartis internal standards
Manage automation‑related changes through Change Control processes
Support production by troubleshooting complex automation issues and optimising system performance
Collaborate with IT/OT and vendors to ensure system availability, cybersecurity and long‑term sustainability
Support internal and external audits and inspections
Coach and technically support junior engineers within the team
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University degree in Automation, Electrical Engineering, Mechatronics, Computer Science or similar
5+ years of relevant experience, with at least 2 years in a GMP‑regulated (pharma, biotech or chemical) environment
Strong hands‑on experience with PLC / SCADA / DCS systems and industrial networks
Experience with computer system validation (CSV) and regulated documentation
Ability to work independently, make sound technical decisions and communicate clearly with multiple stakeholders
Skills Desired