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
Your Key Responsibilities:
Your responsibilities include, but not limited to:
- Planning, execution and evaluation of scientific studies with focus on in-vitro bioequivalence and development studies in the context of the pharmaceutical development of respiratory combination product from early stage up to pilot scale
- Act as core member of the technical project team
- Coordination of development work with internal and external development partners
- Ensure compliance with Regulatory and Quality requirements for technical product development in accordance with internal, national and international guidelines (GMP, ICH, etc.) in order to guarantee successful approval of the respiratory combination product
- Assess and consolidate with the project leader and other key stakeholders all resource needs needed and timelines for assigned projects
- Use the possibilities offered by modern formulation, process and analytical technologies to progress projects in a timely manner
What you’ll bring to the role:
- Minimal BSc degree (PhD preferred) in Chemistry, Pharmacy, or related field or at least 6 years of relevant work-related experience in respiratory combination product development.
- Understanding of Quality-By-Design and product development lifecycle
- Knowledge of in-vitro tests for characterization of Dry Powder Inhaler and of statistical methods relevant for bioequivalence evaluations, Python and R-programming skills would be a plus
- Basic knowledge of relevant guidelines and literature within the above-mentioned field of responsibilities with excellent knowledge in GMP and qualification standards.
- Fluent in spoken and written English and ideally in German
- Presentation skills to communicate effectively to peers and senior management, with the scientific writing skills to complete Regulatory submission documentation
- You are a team player, work independently and are result-orientated
You’ll receive:
Sandoz has an employee-first approach and that’s why your personal growth is so important to us. You will have access to Coursera and other learning platforms with more than 200,000 learning videos and 5000+ courses.
In addition to the various learning opportunities, we offer company benefits, such as:
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30 days of annual leave
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Holiday allowance
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Additional rewards for special occasions (e.g. service length awards, marriage celebration, etc.)
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Company pension schemes and capital formation benefits
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Parental leave
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Other offerings, such as bike leasing
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:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Hiring decisions are only based on the qualification for the position, regardless of gender, ethnicity, religion, sexual orientation, age and disability.
The law provides for severely disabled / equal applicants the opportunity to involve the local representative body for disabled employees (SBV) in the application process. If you would like to request this, please let us know in advance as a note on your CV.
Join our Sandoz Network:
If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Sandoz and our career opportunities, join the Sandoz Network here:
Local position: https://talentnetwork.novartis.com/hiringgermany
#Sandoz
Skills Desired
Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Waterfall Model
Top Skills
What We Do
Novartis is an innovative medicines company. Every day, working to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide.
