Vaše ključne odgovornosti:

• Oceno varnosti in kakovosti proizvedenih serij zdravil.
• Sproščanje posameznih serij zdravil /tehnično sproščanje DP bulk in končnih izdelkov.
• Certificiranja serij/sprostitev končnih izdelkov na trg v skladu z dovoljenjem za promet z zdravilom in regulativnimi zahtevami (EU, FDA, lokalna zakonodaja) za izdelke, ki se bodo proizvajali in/ali sestavljali ter pakirali na lokaciji v Ljubljani in Stein-u.
• Letni pregledi kakovosti izdelkov.
• Reševanje zahtevnejših odstopov, reklamacij in vrednotenje predlogov za spremembe.
• Zagotavljanje učinkovitega sistema kakovosti v skladu z Novartisovimi standardi, zakonodajo, dobrimi farmacevtskimi praksami in poslovnimi cilji.
• Dodatne odgovornosti, ki jih dodeli vodja v skladu z letnimi cilji in kazalniki uspešnosti.

Vaš doprinos k delovnem mestu:

Pričakujemo komunikativne osebe, usmerjene k timskemu delu in doseganju rezultatov, ki so pripravljene sprejemati nove izzive in stremijo k širitvi svojega znanja.

• Visokošolsko izobrazbo farmacevtske smeri.
• Najmanj 3 leta delovnih izkušenj na vsaj enem od naslednjih področjih v farmacevtski industriji: razvoj, proizvodnja, MS&T, kakovost.
• Prednost predstavljajo izkušnje na področju proizvodnje aseptičnih izdelkov in kontrole kakovosti.
• Aktivno znanje angleškega jezika.

Ponujamo zaposlitev za nedoločen čas s 6-mesečno poskusno dobo. Vljudno vabljeni, da oddate svojo prijavo in življenjepis v angleškem jeziku.

Kaj nudimo:

Konkurenčen plačni paket, letni bonus, fleksibilen način dela, z možnostjo prilagajanja urnika in delom od doma, zaposlitev v podjetju s certifikatom TOP Employer, pokojninsko shemo, shemo nagrajevanja in priznanja dosežkov, razširjeni program promocije zdravja na področju telesnega, duševnega in družbenega počutja (Polni življenja) ter dogodke, neomejene priložnosti za učenje in razvoj. 

Predani smo raznolikosti in vključenosti

Novartis si prizadeva ustvariti izjemno, vključujoče delovno okolje in oblikovanje raznolikih timov, saj ti predstavljajo naše bolnike in skupnosti, ki jih oskrbujemo. 

________________________

Key Responsibilities:

• Assessment of the safety and quality of manufactured batches.
• Performing batch release /technical release for DP bulk and aseptic finished products.
• Performing batch certification /release to the market of aseptic finished products in accordance with marketing authorization and regulatory requirements (EU, FDA, local legislation) for products which will be manufactured and/or assembled and packed at both Ljubljana and Stein sites.
• Annual product quality reviews.
• Resolving deviations, complaints and evalsuating change requests.
• Establishing and ensuring an effective quality system in accordance with Novartis standards, legislation, good pharmaceutical practices and business objectives.
• Additional responsibilities as assigned by the supervisor, in line with the annual objectives and performance indicators.

Essential Requirements:

We expect communicative people who are oriented towards teamwork, achieving results and problem solving, who are ready to take on new challenges and strive to expand their knowledge.

• Education in the field of pharmacy.
• Minimum 3 years of professional experience in one or more of the following areas in Pharmaceutical Industry: development, production, MS&T or quality.
• Advantage is work experience in the field of quality control, medical device and aseptic production.
• Active knowledge of English language.

We offer permanent employment, with 6 months of probation period. You are kindly invited to submit your application and CV in English language.

You’ll receive:     

Competitive salary, Annual bonus, Flexible working schedule, tailored to your needs, possibility to work from home, Pension scheme, Employee Recognition Scheme, Expanded program for the promotion of health in the field of physical, mental and social well-being (Wellbeing), employment at Top SI Employer, Unlimited learning and development opportunities.

Commitment to Diversity and Inclusion:

Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.