Your key responsibilities

We are searching for a Senior Scientist (d/f/m) who would join our team working with small molecules.
 

Your responsibilities include, but are not limited to:

• Design, plan, perform and document scientific experiments as well as analysis and interpretation of the results to drive development and validation of analytical methods for solid and liquid dosage forms
• Actively support product development with scientific input and generate scientific documents to hand over to internal and/or external partners
• Report, interpret and present scientific/technical results to management
• Participate in technical teams and fulfill assigned project tasks and responsibilities
• Support generation of international registration documents
• Ensuring adherence to requirements of cGMP, pharmacopoeias, health authorities and company quality system
• Actively participate in knowledge exchange; train and mentor associate scientists and technicians, temporary employees, and employees under training/education

What you’ll bring to the role:

• University degree in chemistry or pharmacy or related science with focus on analytical chemistry or equivalent
• 5+ years of experience in pharma industry, preferably in analytical development, under GMP requirements
• Strong background in development and validation of analytical methods, with hands-on experience in dissolution and chromatographic methods
• A deep understanding of the pharmaceutical development requirements, analytical technological questions as well as scientific and process-oriented thinking
• Passion for supporting the international scientific team in solving pharmaceutical challenge
• Strength in organizational skills and proactive working, hands on attitude as well as excellent communication and team orientation are essential
• Proficient in English (written and spoken), German is a plus

Desirable requirements:

• Audit experience highly appreciated
• Knowledge of dissolution apparatus USP4, IVIVC and QC dissolution method development

Imagine what you could do here at Sandoz!

In addition to a market-competitive base salary, we offer an attractive incentive program, a modern company pension scheme, childcare facilities, learning and development options as well as worldwide career opportunities. In accordance with Austrian law, we are obliged to disclose the minimum salary as stated in the collective bargaining agreement. For this position the minimum salary is € 58,199.96/year (on a full time basis). We also offer a potential market oriented excess payment in line with your experience and qualifications.

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.

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://www.sandoz.com/careers/

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