Vodilni raziskovalec v Regulatorni analitiki (d/ž/m) / Leading Scientist in the Regulatory Analytics group (d/f/m)
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Job Description Summary
Prihodnost je v naših rokah. / The future is ours to shape.Job Description
Iščemo izkušenega, radovednega in navdihujočega Vodilnega raziskovalca v Regulatorni analitiki z močno analitsko ekspertizo in usmerjenostjo v timsko delo, za delo na področju razvoja standardnih in kompleksnih zdravil.
Vaše ključne odgovornosti:
- Učinkovito sodelovanje s člani projektne ekipe, vključno s predstavljanjem ugotovitev in aktivnim sodelovanjem pri reševanju izzivov, ki se pojavijo med razvojem zdravil.
- Sodelovanje pri optimizaciji in prenosu najsodobnejših analitskih metod.
- Pregledovanje in potrjevanje rezultatov, ki jih ustvarijo sodelavci, izpodbijanje sklepov in dajanje priporočil.
- Odlične sposobnosti odpravljanja težav, prepoznavanja in reševanja problemov, vključno z obravnavanjem in reševanjem problemov visoke kompleksnosti.
- Odgovornost za pripravo visokokakovostne registracijske dokumentacije za predložitev HA in opravljanje vloge tehničnega strokovnjaka pri revizijah, inšpekcijskih pregledih itd.
- Delovanje skladno z regulatornimi smernicami in delovanje skladno s ustreznimi standardi, postopki in smernicami kakovosti.
- Dokončanje projektov in dodeljenih nalog v določenih rokih, proračunu in pričakovani kakovosti.
- Izkazovanje proaktivnega in neodvisnega sloga dela z dokazano sposobnostjo uspešnega izvajanja več dejavnosti hkrati, izkazovanja iniciative in zagotavljanja inovativnih rešitev.
- Komuniciranje vizije in vrednot podjetja ter vzpostavljanje in vzdrževanje dobrih odnosov s poslovnimi partnerji.
Vaš prispevek k delovnemu mestu:
- Visokošolska izobrazba na področju naravoslovnih znanosti z dobrim znanjem s področja analitike, farmacije, kemije ali drugih sorodnih naravoslovnih znanosti relevantnih za razvoj standardnih in kompleksnih zdravil.
- Minimalno 6 let ustreznih delovnih izkušenj oziroma 3 leta v primeru doktorata znanosti.
- Poznavanje regulatornih pričakovanj in zahtev.
- Izkušnje z delom v interdisciplinarnih in medkulturnih ekipah.
- Dobre mehke veščine, kar pomeni sposobnost odprtega, jasnega, odločnega, organiziranega in jedrnatega komuniciranja, ki omogoča vpliv na strokovnih srečanjih, ter sposobnost sodelovanja kot samostojna enota med ekipami v globalnem okolju.
- Znanstvena odličnost, digitalna odličnost in operativna odličnost. Sposobnost uvajanja novih pristopov ter prizadevanje za izboljšave in poenostavitve.
- Zahtevano je aktivno znanje angleškega jezika (ustno in pisno).
Kaj nudimo:
Lokacija dela: Ljubljana
Vrsta pogodbe: pogodba za nedoločen čas s 6-mesečnim poskusnim obdobjem
Predvideni tedenski delovni čas: 40 ur
*Plačni razpon: 50.720 – 76.080 EUR bruto
*Plača v Sandozu temelji na nivoju delovnega mesta, kvalifikacijah, specifičnih veščinah in znanjih ter delovnih izkušnjah. Visoko usposobljeni kandidati so običajno umeščeni okoli mediane plačnega razpona, manj izkušeni na spodnji del razpona, kandidati z izrazito močnimi ali nišnimi kompetencami pa višje. Pri umeščanju v plačni razpon upoštevamo tudi notranjo uravnoteženost plač in zunanje tržne podatke.
Naš paket ugodnosti dodatno vključuje:
- Letni bonus (STI): odstotek letne plače
- Regres za letni dopust: leta 2025 je znašal 2.430,99 EUR (neto)
- Božičnica: leta 2025 je znašala 2.100 EUR (bruto)
- OurShare: Vsako leto bo zaposleni v družbi Lek d.d. upravičen do prejema delnic družbe Sandoz AG
- Prostovoljno dodatno pokojninsko zavarovanje: družba Lek d.d. v celoti krije mesečni prispevek za dodatno pokojninsko zavarovanje v višini 5,844 % vaše mesečne bruto plače
- Kolektivno življenjsko in nezgodno zavarovanje (kritje velja 24/7)
- Hibridno delovno okolje, ki omogoča fleksibilnost in možnost dela na daljavo.
Ste pripravljeni na naslednji korak v karieri?
Prijavo z življenjepisom v angleškem in slovenskem jeziku lahko oddate najpozneje do 3. maja 2026.
Zakaj Sandoz?
Sandoz je vodilni svetovni proizvajalec generičnih in podobnih bioloških zdravil – segmenta zdravstvene industrije, ki zagotavlja 80 % vseh zdravil na svetu po 30-odstotni ceni ter s tem vpliva na življenja več kot milijarde ljudi v več kot 100 državah. Čeprav smo ponosni na svoje dosežke, si prizadevamo narediti še več, da bi vsakdo imel dostop do temeljne človekove pravice – pravice do dobrega zdravja.
Z naložbami v nove razvojne zmogljivosti, proizvodne lokacije, nove pridobitve in partnerstva imamo priložnost oblikovati prihodnost Sandoza ter še večjemu številu ljudi omogočiti trajnostni dostop do cenovno ugodnih in visokokakovostnih zdravil.
Naš zagon temelji na odprti kulturi sodelovanja, katere srce so naši talentirani in ambiciozni sodelavci in sodelavke. V okolju, kjer so raznoliki načini razmišljanja dobrodošli in kjer se podpira osebna rast, imajo v zameno za uporabo svojih znanj možnost v celoti izkusiti delo v agilnem in povezovalnem okolju ter razvijati svojo uspešno kariero.
Pridružite se nam in nam pomagajte povečati pravičnost in hitrost zdravstvenega varstva.
Prihodnost je v naših rokah.
Predani smo raznolikosti in vključenosti:
Zavzemamo se za raznolikost, enake možnosti in vključenost. Prizadevamo si za oblikovanje raznolikih timov, saj ti predstavljajo naše bolnike in skupnosti, ki jih oskrbujemo.
#Sandoz
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We are looking for an experienced, curious and inspiring Leading Scientist in the Regulatory Analytics group with advanced analytical expertise and team-oriented mindset, to contribute to the development of standard and complex drug products.
Your key responsibilities:
- Effectively collaborating with cross‑functional project teams, including presenting scientific findings and actively contributing to the resolution of challenges arising during drug development.
- Supporting the optimization and transfer of state‑of‑the‑art analytical methods across development and quality functions.
- Reviewing and approving results generated by colleagues, challenging conclusions and provide recommendations.
- Applying advanced problem‑solving skills to identify, analyze, and resolve highly complex scientific and technical issues.
- Taking accountability for the preparation of high‑quality regulatory documentation for submission to Health Authorities (HA). Acting as a technical subject‑matter expert during audits, inspections, and regulatory interactions
- Acting in full compliance with regulatory requirements and adheres to applicable quality standards, procedures, and guidelines.
- Delivering assigned projects and tasks within agreed timelines, budgets, and quality expectations
- Demonstrating a proactive and independent working style, with proven ability to successfully manage multiple activities in parallel.
- Communicating company vision and values; establish and manage good relationships with business partners.
What you will bring to the role:
- A university degree in natural sciences with strong knowledge of analytics, pharmacy, chemistry, or other related natural science disciplines relevant to the development of standard and complex drug products.
- Minimum 6 years of relevant experience or 3 years in case of PhD.
- Understanding of regulatory expectations and requirements.
- Experience with working in interdisciplinary and cross-cultural teams.
- Strong soft skills, means the ability to communicate in an open, clear, assertive, organized and concise manner to be influential in scientific meetings and ability to work together as one team in a global environment.
- Demonstrated scientific excellence combined with digital and operational mindset to drive efficient analytical development.
- Active knowledge of English language required (oral & written).
What we offer:
Job location: Ljubljana
Contract type: permanent contract with 6-month probation period
Expected weekly working hours: 40
*Pay range: €50,720 – €76,080 gross
*Salary at Sandoz is based on job level, qualifications, specific skills, and work experience. Fully proficient candidates are usually placed around the market median, less experienced candidates lower in the range, and those with strong or niche expertise higher. When determining placement within the range, we also consider internal pay equity and external market data.
Our compensation package additionally includes:
- Annual bonus (STI): percentage of annual salary
- Vacation allowance: in 2025 it was €2,430.99 net
- Christmas bonus: in 2025 it was €2,100 gross
- OurShare: every year, an employee of Lek d.d. will be entitled to receive shares of Sandoz AG
- Voluntary Additional Pension Scheme: The company fully covers the contribution for your supplementary pension plan, amounting to 5.844% of your gross salary
- Collective life and accident insurance (24/7 coverage)
- A hybrid work environment offering flexibility and remote work possibilities
Ready for your next career move?
You are kindly invited to submit your application in English and Slovene, including a CV, by May 3, 2026.
Why Sandoz?
Sandoz is the global leader in Biosimilar and Generic medicines, a segment of the healthcare industry that delivers 80% of the world’s medicines at 30% of the cost, touching the lives of more than 1 billion people across 100+ countries! While we are proud of our achievements, we have the ambition to do more so that everyone can benefit from the basic human right of good health.
With investments in new development capabilities, production sites, new acquisitions and partnerships, we have the opportunity to shape a sustainable future for Sandoz and to help even more people gain access to low-cost, high-quality medicines.
Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues who, in return for applying their skills, experience an agile and collegiate environment where diversity of thought is welcomed and where personal growth is supported!
Join us in helping to make healthcare fairer and faster.
The future is ours to shape.
Commitment to Diversity & Inclusion:
We are committed to building an outstanding, inclusive work environment and to forming diverse teams that are representative of the patients and communities we serve.
#Sandoz
Skills Desired
About Sandoz
Global leader in generic and biosimilar medicines, operating as an independent company spun off from Novartis. Based in Basel.