Regulatory Affairs Specialist

Dettagli della offerta

Job Description Summary
Sandoz is going through an exciting and transformative period as a global leader and pioneering provider of sustainable Generic and Biosimilar medicines.
Now as an independently listed company, Sandoz aims to increase its strategic focus, operate with greater agility, set clearer business objectives, enhance shareholder returns, and strengthen its culture for us, the Sandoz associates. This is an exciting time in our history, and by creating a new and ambitious path, it will provide a unique opportunity for us all, both professionally and personally.
Join us as a Founder of our 'new' Sandoz!
Job Description
Role Purpose
The Country Regulatory Affairs Specialist is responsible for the execution of specific Regulatory Affairs activities at Sandoz country level.
Tasks assigned will support in maintaining the registered products, related texts and artworks, and (supporting) the execution of projects.
Your Key Responsibilities
Your responsibilities include, but are not limited to:
Team and culture
Be seen as an RA expert
Compliance:
Guarantees regulatory compliance in execution versus standards required for regulatory submissions and ensures adherence to Sandoz standards, and local health authority legislation and expectations.
Guarantees adherence to the relevant (local) procedures, and record management.
Supports RA during internal and external audits and health authority inspections at country level.
Activities to support Sandoz and our customers
Guarantees timely creation & translation of official product information including Patient Information Leaflets, Summary of Product Characteristics (SmPCs) and all labelling (packaging texts into artworks).
Maintenance of registration files (mainly MRP and DCP) by: Registration maintenance activities, product related text translations, answering questions from local health authorities, updating regulatory databases and plans, local regulatory tasks related to Risk Management Plan (RMP)/ Risk Minimization Activities (RMA) and Dear Healthcare Professional Communications (DHPC) (as per global SOP).
Guarantees timely implementation of changes of the registered text into artworks.
For the activities in scope of the role ensures that all relevant Key Performance Indicators (including safety label changes, artwork, checklists, deviations, RA input in RMP implementation and DHPC communication), are achieved timely & correctly and that all GxP and RA relevant documents are archived as per specifications.
Commitment to Diversity & Inclusion:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
What you'll bring to the role:
Essential Requirements:
University Degree, Bachelor or Master in Bio-Medical / Life Sciences / Pharmaceutical sciences.
Preferably >1 year of relevant work experience.
Italian and English fluent (verbal and written).
Previous experience in a highly regulated environment.
Planning, organizational skills and eye for detail.
Accountability for actions, setting own priorities and decision taking.
Result oriented.
High ethical standards.
You'll receive:
Customized development paths and free access to our on-demand training catalogs.
Job rotation projects that will give you the opportunity to collaborate with global teams.
Corporate Welfare Plan.
Recognition Program to highlight your impact for the organization.
Hybrid Work Model based on flexibility and trust.
Why Sandoz?
Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, touched the lives of almost 500 million patients last year and while we are proud of this achievement, we have an ambition to do more!
With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.
Our momentum and entrepreneurial spirit 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 with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is encouraged!
The future is ours to shape!
Join our Sandoz Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Sandoz and our career opportunities, join the Network here: Sandoz Talentpool (novartis.com)
#Sandoz

#J-18808-Ljbffr


Salario Nominale: Da concordare

Risorsa: Allthetopbananas_Ppc

Funzione Lavorativa:

Requisiti

Addetto Underwriting & Claims | Inglese Fluente

La tua nuova azienda Il nostro cliente è una nota Compagnia Assicurativa con casa madre in Germania leader nel mercato assicurativo di soluzioni a tutela dal...


Hays - Lombardia

Pubblicato 10 days ago

Corporate Counsel, Aws Legal

Job ID: 2817781 | AWS EMEA SARL (Italy Branch) Amazon Web Services (AWS) is at the forefront of the cloud computing industry providing IT infrastructure serv...


Amazon - Lombardia

Pubblicato 10 days ago

Junior Associate - Environmental Law And Town Planning (Public Law And Regulatory)

Junior Associate - Environmental Law and Town Planning (Public Law and Regulatory)Are you ready to grow with the world's largest law firm? Join Dentons Italy...


Dentons Canada - Lombardia

Pubblicato 10 days ago

Visa Cash App Rb F1 Team - Operatore Modelleria

Visa Cash App RB F1 è uno dei due team F1 di proprietà Red Bull. La Formula 1 odierna richiede un alto livello di competenze specialistiche in ogni settore. ...


Motorsport-Total.Com Gmbh - Lombardia

Pubblicato 10 days ago

Built at: 2024-11-25T12:40:18.241Z