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Novartis is recruiting a Senior Expert in Upstream Process Development for Schaftenau, Austria to lead late‑phase cell culture process development, scale‑up and tech transfer for biotherapeutics across clinical and commercial supply chains.
You will collaborate with global teams, mentor staff, and drive regulatory‑relevant documentation while advancing platform technologies and process innovations.
Salary Range:
€66,918.00 - €117,800.00
With over 25 years of experience in cell culture process development and several commercialized products on the market, we are dedicated to scientific excellence and innovation. This is your opportunity to join the Drug Substance Upstream Process Development team in Schaftenau as a Senior Expert Science & Technology (m/f/d), where your expertise will directly contribute to delivering life-changing medicines to patients around the world.
As a Senior Expert in Upstream Process Development, you will lead all USP‑related activities for late‑phase development—driving process characterization and ensuring seamless transfer of robust cell culture processes for clinical and commercial supply.
You will work in cross‑functional teams and collaborate closely with internal stakeholders, as well as external partners, to deliver excellence at every stage of development. A key responsibility of this role is to ensure the successful transfer of in‑house and in‑licensed upstream processes to internal manufacturing sites, thereby enabling global patient access to innovative medicines.
24 Month Fixed Term Contract
#LI-Hybrid
Location - Schaftenau, Austria
Your responsibilities will include, but are not limited to:
Lead late‑phase upstream process development and characterization, including scale up and tech transfer for manufacturing of biotherapeutics, and serve as USP subject matter expert within cross‑functional teamsDrive upstream development for portfolio and innovation projects, leveraging lab‑and pilot‑scale capabilities to generate high‑quality data for process understanding and model developmentUtilize modeling and simulation tools to support in‑silico process development and transferAuthor, review and approve technical, scientific and regulatory‑relevant documents incl. risk assessmentsCollaborate across functions and geographies to translate lab‑scale insights into robust, scalable production processesContribute to the strategic evolution of upstream platform technologies, innovation initiatives, and global guidelines. This includes active participation in global USP functional network and focus groups
Drive bioprocess scale up and transfer of cell culture processes within our internal bioproduction networkEvaluation of process characterization data, development reports, and associated documentation to ensure alignment of external processes with internal standardsSupport roll‑out and implementation of PAT technologies as part of process transfers
Mentor and coach junior scientific associatesContribute to scientific publications, conference presentations and intellectual property generationCommunicate effectively across organizational interfaces; lead troubleshooting and transfer of know‑how to/from other departments or external partner
University degree in life sciences (biotechnology, bioprocess engineering, or equivalent); PhD with min. 2 years or Master with min. 6 years industrial experience or equivalentProven experience in upstream process transfer and collaboration with manufacturing partners
Fluent in English and German
Profound knowledge and hands on experience in bioprocess engineering principles and upstream unit operations; knowledge in cell culture process late‑phase developmentExperience with statistical methods (DoE, MVDA) as well as with data‑driven or mechanistic modelsExcellent communication, presentation, project management as well as ability to work collaboratively in cross‑functional teamsExperience with use of mechanistic, data‑driven, and hybrid models for in‑silico process development and optimization would be a plus
Expected Annual Base Salary Range for role:
66,918.00 – 117,800 EUR
In addition to a market‑competitive base salary, we offer an attractive incentive program, a modern company pension scheme, childcare facilities, learning and development opportunities as well as worldwide career possibilities within the Novartis group.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 € 65,605.54 EUR/year (on a full‑time basis). The actual salary will be significantly higher, as we strive to maintain a competitive position in the market and consider your previous experience, qualifications and individual competencies.We are open for part‑time and job‑sharing models and support flexible and remote working where possible.
Novartis is committed to building an outstanding, inclusive work environment and diverseteams’representative of the patients and communities we serve.
If because of a medical condition, physical disability or a neurodiverse condition you require an adjustment during the recruitment process, please reach out to disabilities.austria@novartis.comand let us know the nature of your request as well as your contact information. The support which we can provide will include advice on suitable positions as well as guidance at all stages of the application process. Austrian law provides candidates the opportunity to involve the local disability representative,Behindertenvertrauensperson(BVP), in the application process. If you would like to request this, please let us know in advance as a note on your CV.