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Scientist AD (d/f/m)

Posted 6 Days Ago
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Sandoz, CA
Entry level
Sandoz, CA
Entry level
As a Scientist AD, you will contribute to the development of generic drug products by conducting analytical and stability activities, collecting and interpreting data, preparing reports, collaborating with cross-functional teams, and assisting in regulatory submissions while ensuring compliance with quality standards.
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Job Description Summary

The future is ours to shape.


 

Job Description

Sandoz, of which Lek is also a part, 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 and Lek 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. 

As Sandoz Global Development organization, we are responsible for development & delivery of high-quality pharmaceutical drug products. We are looking for curious and inspiring Scientist AD with strong analytical expertise and team-oriented mindset, to contribute to the development of generic drug products. Join us as a Founder of ournewSandoz and Lek!  

Your key responsibilities: 

Your responsibilities include, but not limited to: 

  • Be a vital member of a cross-functional project team in the development of generic drug products, covering analytical and stability activities in late phase development.
  • Collect, evaluate and interpret analytical/stability data.
  • Coordinate analyses of stability samples (applying state-of-the-art analytical methods (e.g. (U)HPLC, LC-MS, GC-MS, IC, CE,…)).
  • Conduct thorough data reviews and documentation of results, as well as prepare scientifically supported and well-structured analytical/stability reports that adhere to the required documentation principles.
  • Effectively collaborate with other project team members, including presenting findings and active involvement in solving shared challenges that arise during development of the drug product.
  • Deliver drug product project activities in alignment with the project plan.
  • Assist in preparation of registration documents for HA submissions and act as a technical expert during audits and inspections.
  • Stay up-to-date with scientific publications and advancements for the studied field of research.
  • Demonstrate digital proficiency and operational excellence in your work.
  • Ensure compliance of activities with standards in the field of quality (GMP), in the field of ensuring health and safety at work and other Sandoz standards.

 

What you will bring to the role: 

  • Advanced degree in life sciences with strong background in biotechnology, biology, biochemistry, analytics, pharmacy, chemistry or other related Life sciences.
  • Understanding of regulatory expectations and requirements.
  • Excellent scientific/technical writing skills.
  • Experience with working in interdisciplinary and cross-cultural teams
  • Strong soft skills and 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.
  • Scientific Excellence, Digital Excellence and Operational Excellence, as well as the ability to implement new approaches, while striving for improvement and simplifications.
  • Active knowledge of English language required (spoken and written).

 

You’ll receive: 

Employment at the most reputable employer in Slovenia offers 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 (Energized for Life), Unlimited learning and development opportunities. 

 

Possible job locations: Slovenia (Ljubljana) 

 

We offer permanent contract with 6 months of probation period. You are kindly invited to submit your application in English language, including CV, by 28 February 2025. 

 

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! 

 

Commitment to Diversity & Inclusion:  

Sandoz is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve. 

 

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: https://talentnetwork.novartis.com/sandoztalentpool  

 

#Sandoz 


 

Skills Desired

Top Skills

Ce
Gc-Ms
Ic
Lc-Ms
Uplc

Novartis London, England Office

The WestWorks, White City Place, London, United Kingdom, W12 7FQ

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