Jobs / United States / Novartis Pharmaceuticals Corporation
Ekspert za oskrbo zdravil (m/ž/d) / Expert Drug Supply (m/f/d)
Novartis Pharmaceuticals Corporation · 🇺🇸 Mengeš
Sponsorship verdict
Sponsorship possible
One solid signal, not two — worth applying, and worth asking about sponsorship early.
- Employer is on a government sponsor recordThe US Department of Labor certified 75 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 31 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
- The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
- No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
- What Novartis Pharmaceuticals Corporation paid sponsored hires in similar roles1 certified filing for “Expert Science & Technology” (Bioengineers and Biomedical Engineers) in NC: $113k–$113k, median $113k. Most were filed at wage level III (100%) — 3 lottery entries, ≈46% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).
- Confirmed live todayWhen a source last listed this job as open.
US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).
A verdict summarises public evidence; it is not legal advice and never a guarantee — the employer and the immigration authority decide. Sign in to factor in where you can already work.
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Sponsor Radar — Novartis Pharmaceuticals Corporation
The US Department of Labor certified 75 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 31 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Novartis Pharmaceuticals Corporation →
About the role
Salary Range: €27,160.00 - €50,440.00 Job Description Summary Z veseljem sporočamo, da smo v Sloveniji odprli nov klinični proizvodni obrat, namenjen pospeševanju ustvarjanja inovativnih zdravil za paciente po vsem svetu. Ta najsodobnejši obrat, ki se nahaja v Biocampusu Mengeš, ponuja neprimerljive priložnosti za sodelovanje, inovacije in vpliv. Trenutno iščemo motivirane in usposobljene strokovnjake za ekipo za klinično proizvodnjo zdravilnih učinkovin na naši lokaciji TRD v Mengšu v Sloveniji. Kot Eskpert za oskrbo z zdravili boste procesni specialist v klinični proizvodnji zdravilnih učinkovin. Vaše ključne odgovornosti vključujejo mikronačrtovanje, podporo izvajanju in nadzor proizvodnega procesa ali dejavnosti kvalifikacije proizvodne opreme, ter podporo drugim dejavnostim (npr. change over, upravljanje odstopanj v proizvodnji). Postanite del dinamičnega tima, ki na novo opredeljuje zdravljenje in prinaša upanje tistim, ki ga najbolj potrebujejo. Pridružite se nam pri oblikovanju prihodnosti zdravstva in ustvarjanju pomembnih sprememb v življenju pacientov po vsem svetu. Veselimo se, da vas bomo pozdravili v naši ekipi! We are thrilled to announce the establishing of new clinical manufacturing facility in Slovenia, dedicated to accelerating the creation of innovative medicines for patients around the globe. This cutting-edge facility, located at Biocampus Mengeš, offers unparalleled opportunities for collaboration, innovation, and impact. We are currently looking to hire passionate and skilled specialists in the Drug Substance Clinical Manufacturing Team at our TRD site in Mengeš, Slovenia. As Expert Drug Supply, your role will be a process specialist within the Drug substance clinical production, with key responsibilities including microplanning, supporting the execution and overseeing the production process or production equipment qualification activities, as well as supporting other activities (e.g. change over, management of deviations within the production). Be part of a dynamic team that is reimagining medicine and delivering hope to those who need it most. Join us in shaping the future of healthcare and making a meaningful difference in the lives of patients worldwide. We look forward to welcoming you to our team! #LI-Hybrid Menges, Slovenia Job Description Vaše ključne odgovornosti: • Načrtovanje, razporejanje in usklajevanje proizvodnega procesa, kvalifikacij, validacij in drugih aktivnosti ekipe. • Samostojno ocenjevanje in interpretiranje rezultatov ter sprejemanje ustreznih zaključkov. • Zagotavljanje znanstvenega in tehničnega vodenja; iskanje informacij, aktivno spodbujanje izmenjave znanja znotraj skupine. • Sodelovanje v multidisciplinarni ekipi in zagotavljanje podpore, mentorstva in nadzor mlajšim članom. Prenašanje znanja znotraj ekip in na druge deležnike. • Samostojno pisanje protokolov, zapisov glavnih serij, standardnih operativnih postopkov, proizvodnih receptov in druge dokumentacije. Aktivnor sodelovanje pri revizijah in zagotavljanje skladnosti. • Komuniciranje, obravnavanje in reševanje odstopanj. Prispevanje k odpravljanju težav, preiskavam temeljnih vzrokov in predlaganje korektivnih ukrepov. • Prevzemanje odgovornosti, odprte komunikacije in kulture reševanja problemov/osredotočenosti na rezultate, pri čemer je kakovost glavna prednostna naloga. • Prevzemanje odgovornost za osebni in poklicni razvoj. Vaš doprinos k delovnem mestu: • Univerzitetna izobrazba s področja farmacije, biokemije, biotehnologije, kemije, mikrobiologije ali druge enakvoredne smeri. • Tehnično znanje angleščine. • Več let sorodnih izkušenj kot strokovnjak za proizvodnjo bioloških zdravil. Zaželene izkušnje: • Poznavanje dobre proizvodne prakse (GMP) in izkušnje z delom v reguliranem proiz