Novartis

Healthcare

Laboratorijskianalitik(m/ž/d)

€24–32k ~AI est. Mengeš, Slovenia FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Laboratorijski analitik (m/ž/d) at Novartis. Skills: Chromatography, Quality control. Ensure activities comply with cGxP. Ensure data integrity”

Industry & Context.

Healthcare
Eligibility Requirements

6-month probation period

What They're Looking For.

Must Have

High School diploma, Basic English language skills, Active Slovenian language skills, Microsoft Office tools knowledge

Nice to Have

GMP processes knowledge, Gas and liquid chromatography basics knowledge

What You'll Do.

Ensure activities comply with cGxP

Ensure data integrity

Process and verify results

Enter results into information system

Maintain laboratory logbook

Coordinate activities with GMP regulations

Coordinate activities with Novartis standards

Follow and implement HSE rules

Follow and implement HSE guidelines

How You'll Work.

Team & Collaboration

Experienced analytics team

Full Job Description

**Job Description Summary** #LI-Onsite Lokacija: Mengeš V našem kromatografskem laboratoriju skrbimo za to, da imajo bolniki dostop do kakovostnih, varnih in učinkovitih zdravil za težko ozdravljive bolezni. S pomočjo najsodobnejših analitskih tehnik preverjamo kakovost farmacevtskih učinkovin in s tem pomembno prispevamo k razvoju ter proizvodnji zdravil. Kot Laboratorijski analitik v oddelku kontrole kakovosti v Mengšu boste postali del izkušene ekipe strokovnjakov za analitiko malih molekul, kjer boste imeli priložnost delati z različnimi kromatografskimi metodami (HPLC, GC, IC) in poglabljati svoje znanje na področju farmacevtske analitike. Dinamično delo, podprto z nenehnim strokovnim razvojem in sodobno opremo, ponuja okolje, v katerem boste lahko rasli tako osebno kot profesionalno. This role is based in Mebše, Slovenia. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. **Job Description** **Vaše ključne odgovornosti:** * Zagotavljanje, da so vse dejavnosti v skladu s trenutnimi dobrimi praksami (cGxP), ter v skladu z integriteto podatkov. * Skrb za pripravo materiala, opreme in pribora za delo. * Priprava, pregledovanje in analiziranje vzorcev. * Obdelovanje in preverjanje rezultatov. * Vnašanje rezultatov v informacijski sistem. * Vodenje laboratorijskega dnevnika. * Usklajevanje dejavnosti z regulativami dobrih proizvodnih praks (GMP) in Novartisovimi standardi. * Upoštevanje in izvajanje pravil ter smernic za področje zdravja, varnosti in okolja (ZVO). **Vaš doprinos k delovnem mestu:** * Srednješolska stopnja izobrazbe farmacevtske, kemijske, veterinarske ali druge ustrezne smeri. * Osnovno znanje angleškega jezika. * Aktivno znanje slovenskega jezika. * Poznavanje orodja Microsoft Office. **Zaželene izkušnje:** * Poznavanje GMP procesov. * Poznavanje osnov plinske in tekočinske kromatografije. Z izbranim kandidatom bomo sklenili delovno razmerje za določen čas s poskusno dobo 6 mesece

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