Your key responsibilities

Your responsibilities include, but are not limited to:

• Design, plan, perform and document scientific experiments as well as analyze and interpret the results to drive development and validation of analytical methods for simple and complex generics (small molecules).
• Provide active support to product development by offering scientific input and generating comprehensive scientific documents for internal and/or external partners.
• Effectively report, interpret, and present scientific/technical results to management in a clear and concise manner.
• Participate in technical teams and fulfill assigned project tasks and responsibilities.
• Support the generation of international registration documents, ensuring compliance with cGMP, pharmacopoeias, health authorities, and company quality system requirements.
• Actively engage in knowledge exchange activities, training, and mentoring of associate scientists, technicians, temporary employees, and employees under training/education.
• Conduct investigation of OOS/OOE results, identifying root causes and implementing appropriate corrective actions.
• Actively participate in audits and inspections, demonstrating compliance with industry standards and regulations.

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 challenges.
• 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.

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!

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.

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: www.sandoz.com/careers

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