Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunities will present themselves, both professionally and personally. Join us, the future is ours to shape!

Your Key Responsibilities:

Your responsibilities include, but not limited to:

• Provide expert knowledge for bioanalytical methods and data evaluation (PK/PD and immunogenicity) to global program teams as bioanalytical representative and define the bioanalytical and immunogenicity non-clinical and clinical program strategy throughout different stages in biosimilar development.
• Point of contact for early phase/post-approval programs across divisions (represent Clinical Bioanalytics in global teams and fulfill all project tasks and responsibilities related to the own discipline)
• Assess and consolidate resource needs and timelines for project(s), network(s) and/or platform(s); support budget forecast
• Independently lead assigned functional sub-teams and handle several activities at a time
• Proactively identifies potential project hurdles, provides solutions and implements contingency plans
• Interpret results, evaluate data, and draw relevant conclusions; perform complex tasks without having established procedures. Review analytical results; critically evaluate results and challenge conclusions
• Write excellent scientific reports, briefing books for health authority interactions and registration documents (e.g. Integrated Summary for Immunogenicity)
• Participate in audits, inspections and due diligence activities
• Present scientific results internally and externally and publishes internally or externally as main contributor to enhance Sandoz and Clinical Bioanalytics visibility; may require up to 5% travel
• Provide scientific and technical guidance; actively drive knowledge exchange.
• Identify and resolve conflict situations with empathy. Collaborate within own and with other groups.
• Work according to appropriate standards as defined in Quality Manual, SOPs, ethical, health, safety, environment (HSE), and information security (ISEC) guidelines; lead initiatives to proactively ensure compliance and continuous improvement; advise team members and ensure all own and team activities are aligned with overall drug development process

What you’ll bring to the role:

Essential Requirements:

• Science degree with PhD and 6 years relevant industrial experience or equivalent technical education and industrial experience and a known expert in the scientific community
• Fluent in English (oral and written)
• Thorough understanding of development activities and processes in a specific function and broad scientific and strategic background
• Excellent theoretical and scientific knowledge in the relevant area as well as good scientific project management skills
• Very good knowledge on relevant regulatory
  guidelines and understanding of regulatory expectations
• Excellent knowledge and experience with
  laboratory and/or technical tools.
• Good knowledge of software and computer tools.
• Excellent presentation skills
• Proficient scientific/technical writing skills
• Demonstrated successful experience with working in interdisciplinary teams, problem solving and productivity in projects.

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:

• 30 days of annual leave
• Holiday allowance
• Additional rewards for special occasions (e.g. service length awards, marriage celebration, etc.)
• Company pension schemes and capital formation benefits
• Parental leave
• 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, provided more than 900 million patient treatments across 100+ countries in 2024 and while we are proud of this achievement, we have an ambition to do more!

With investments in new development capabilities, 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 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 supported!

Join us!

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.

Fellow Program Management Bioanalytics temporary until 08.2027 (m/f/d)