Job Description Summary

Job Description

Opis delovnega mesta

Kot ključni tehnični strokovnjak v visokotehnološkem centru za proizvodnjo učinkovin za podobna biološka, v oddelku Bioproces, boste povezovali proizvodnjo in podporne funkcije ter s svojim znanjem in izkušnjami prispevali k optimizaciji procesov, reševanju kompleksnih tehničnih izzivov ter nenehnemu izboljševanju učinkovitosti in operativne odličnosti.

Vaše ključne odgovornosti:

Vaše odgovornosti bodo med drugim naslednje:

• Zagotavljanje tehnične in operativne strokovne podpore oddeleku proizvodnje Bioproces z namenom zagotavljanja varne, skladne, zanesljive in učinkovite proizvodnje ter spodbujanja nenehnih izboljšav in operativne odličnosti.
• Vodenje in podpora pri prenosih tehnologij (technology transferjih), validacijah procesov ter uvajanju novih izdelkov in tehnologij, ob tesnem sodelovanju z medfunkcijskimi ekipami pri oceni in optimizaciji vplivov sprememb proizvodnih procesov.
• Spremljanje procesnih rezultatov, analiziranje trendov, sodelovanje pri obravnavi odstopov ter izvajanje korektivnih in preventivnih ukrepov (CAPA).
• Priprava, posodabljanje in vzdrževanje proizvodne, validacijske ter druge podporne dokumentacije v skladu z internimi in regulatornimi zahtevami.
• Sodelovanje pri upravljanju sprememb, validacijah, kvalifikacijah, preiskavah odstopov in aktivnostih za zagotavljanje skladnosti kakovosti.
• Prispevanje k pripravljenosti na inšpekcije, presoje in regulatorne preglede ter sodelovanje pri izvajanju dogovorjenih ukrepov.
• Izvajanje prenosa znanja, podpora usposabljanju sodelavcev ter sodelovanje pri razvoju kompetenc in uvajanju novih zaposlenih.
• Aktivno sodelovanje pri projektih nenehnih izboljšav, optimizaciji procesov ter implementaciji novih tehnologij in rešitev za povečanje učinkovitosti, kakovosti in varnosti.
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Vaš prispevek k delovnemu mestu:

• Univerzitetna diploma iz inženiringa, farmacevtske tehnologije, kemije, farmacije ali druga ustrezne znanstvene smeri. Zaželen magisterij ali ustrezne izkušnje.
• Minimalno 3 leta delovnih izkušenj na delovnih mestih za podporo procesom v proizvodnji in/ali kakovosti.
• Poznavanje procesov (farmacevtska proizvodnja, GMP, regulatorni vidiki).
• Aktivno znanje angleškega jezika in znanje lokalnega jezika.
• Poznavanje orodja Microsoft Office.

Kaj nudimo:

Lokacija dela: Lendava.

Vrsta pogodbe: pogodba za določen čas s 6-mesečnim poskusnim obdobjem.

Predvideni tedenski delovni čas: 40 ur.

*Plačni razpon: 28.880 – 43.320 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 2026 znaša 2.450,00 EUR (neto).
• Božičnica: leta 2025 je znašala 2.100,00 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.
• Dodatek za izmensko delo (15 %); turnusno delo (20 %), nočno delo (70 %), delo ob nedeljah in praznikih (50 %), nadurno delo (30 %).
• Kolektivno življenjsko in nezgodno zavarovanje (kritje velja 24/7).

Ste pripravljeni na naslednji korak v karieri?
Prijavo z življenjepisom v angleškem in slovenskem jeziku lahko oddate najpozneje do 9. oktobra 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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Process Expert (m/f/d)

Job Description

As a key technical expert in a state-of-the-art biosimilar drug substance manufacturing center, within the Upstream Process department you will bridge manufacturing operations and supporting functions, leveraging your expertise to optimize process performance, solve complex technical challenges, and contribute to operational excellence.

Your key responsibilities:

Your responsibilities include, but are not limited to:

• Provide technical and operational expertise for upstream manufacturing processes to ensure safe, compliant, reliable, and efficient production while driving continuous improvement and supporting operational excellence initiatives.
• Drive and support technology transfers, process validations, new product and technology implementations, while collaborating with cross-functional teams to assess and optimize the impact of manufacturing process changes
• Monitoring process performance, analyzing trends, supporting deviation investigations, and implementing corrective and preventive actions (CAPA).
• Preparing, updating, and maintaining manufacturing, validation, and other supporting documentation in compliance with internal standards and regulatory requirements.
• Participating in change management activities, validations, qualifications, deviation investigations, and quality compliance initiatives.
• Contributing to inspection, audit, and regulatory readiness, as well as supporting the implementation of agreed actions and improvements.
• Facilitating knowledge transfer, supporting employee training, and contributing to competency development and onboarding activities for new associates.
• Actively participating in continuous improvement projects, process optimization initiatives, and the implementation of new technologies and solutions to enhance efficiency, quality, and safety.

What you will bring to the role:

• University degree in Engineering, Pharmaceutical Technology, Chemistry, Pharmacy, or another relevant scientific discipline. Master’s degree preferred or equivalent relevant professional experience.
• Minimum of 3 years of experience in manufacturing process support and/or quality-related roles.
• Knowledge of pharmaceutical manufacturing processes, GMP requirements, and regulatory frameworks.
• Fluency in English and proficiency in the local language.
• Proficiency in Microsoft Office applications.

What we offer:

Job location: Lendava.

Contract type: temporary contract with 6-month probation period.

Expected weekly working hours: 40.

*Pay range: €28.880 – €43.320 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 2026 it is €2,450.00 net.
• Christmas bonus: in 2025 it was €2,100,00 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.
• Allowance for shift work (15%); rotational shifts (20%), night shift work (70%), Sunday/public holiday work (50%), overtime work (30%).
• Collective life and accident insurance (24/7 coverage).

Ready for your next career move?
You are kindly invited to submit your application in English and Slovene, including a CV, by October 9th, 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