Job Description Summary
Join us in helping to make healthcare fairer and faster. / Pridružite se nam in nam pomagajte povečati pravičnost in hitrost zdravstvenega varstva.
Job Description
Your knowledge and experience will contribute to a groundbreaking project at our new development centre for biosimilars in Slovenia, where you will help set new industry standards and shape the future of healthcare.
This is the largest investment in the region in the field of biosimilars, bringing together cutting-edge technology, innovative approaches, and experts from diverse disciplines. You will join an environment where science meets vision and help shape its future, with exciting career opportunities.
As a Principal Scientist in Drug Product Development at the Biosimilars Technical Development Centre in Slovenia (d/f/m) you will play a key role in leading and guiding Biosimilar drug product projects and functional activities while actively contributing to strategic decision-making. Your responsibilities will cover the full spectrum of research work—from planning, designing, and execution to precise documentation and independent interpretation of complex scientific and development tasks using state-of-the-art approaches. In addition, you will take responsibility for mentoring and training team members, fostering their professional growth and development.
Your key responsibilities:
Develop Biosimilar Drug Products according to assigned project work packages and in alignment with project strategy, objectives and timelines.
Leading of Drug Product development project activities and alignment of activities between functional experts, team leaders, and project management. Supervise project-related scientific activities and provide technical leadership for sub-teams.
Independently plan, execute, document, and interpret complex development activities using state-of-the-art approaches.
Interpret and evaluate complex data, draw relevant conclusions, provide expert recommendations, and challenge conclusions made by other scientists.
Mentor, train, and develop team members while promoting knowledge sharing within and beyond the organization.
Write and review technical documents , procedures, scientific reports, publications, and patents, and represent the function at internal and external meetings.
Act as a technical expert in audits , inspections, alliances and/or due diligence activities as needed.
Plan and lead initiatives for continuous improvement and the implementation of new technologies, ensuring efficient resource utilization and achievement of project goals within timelines, budgets, and quality standards.
Working in compliance with legislation, internal policies, quality standards, safety, and ethical requirements .
What you will bring to the role:
Master’s degree or PhD in a relevant natural science such as Molecular biology, Chemical engineering, Biochemistry, Biotechnology or Pharmacy.
Minimum of 8 years of experience with a Master’s degree or at least 5 years of experience with a PhD in the field of drug product development, ideally experience in the field of process transfers and late phase process development.
Project management skills
Fluent English language skills.
Proficiency in Microsoft Office tools.
What we offer:
Job location: Ljubljana
Contract type: permanent contract with 6-month probation period
Expected weekly working hours: 40
*Pay range: €50,720 – €76,080 gross per year
* Salary at Sandoz is based on job level, qualifications, specific skills, and work experience. Fully proficient candidates are usually placed around the market median, less experienced candidates lower in the range, and those with strong or niche expertise higher. When determining placement within the range, we also consider internal pay equity and external market data.
Our compensation package additionally includes:
Annual bonus (STI): percentage of annual salary.
Vacation allowance: in 2026 it was €2,450.00 net.
Christmas bonus: in 2025 it…