Summary Location: Schaftenau, Austria
As a Senior Expert you will be part of a team developing new Biologic drugs. The Analytical Operations team is responsible for releasing the product for clinical trial and investigating the stability behavior of the drugs. We also validate the methods used for release and are responsible for transferring those methods to our commercial organization or external partners.
About The Role Key responsibilities
Independently manage key tasks for projects (e.g., release, stability studies, validation, and transfer activities).
Write protocols, scientific reports, lab procedures and prepare ready‑to‑submit documents for releases or stability documents and transfer reports.
Approve GMP documents and test records; investigate quality events within the project (e.g., deviations, changes, out‑of‑spec events).
Support the lab team in troubleshooting existing methods, processes, or solving higher‑complexity problems within projects.
Essential Requirements
Master’s degree in biotechnology, biochemical engineering, biology, chemistry, biochemistry or a related field with at least 4 years of relevant industry experience, or PhD in a relevant field with 2+ years experience in pharmaceutical industry.
Proficiency in English and German is beneficial.
Good knowledge of pharmaceutical, chemical analytics, QC or equivalent technical and scientific principles.
Proven experience within a GMP environment.
Strong theoretical and scientific knowledge in expertise areas (e.g., HPLC, CE).
Desirable Requirements
Can‑do mindset with strong communication across organizational interfaces and presentation skills.
Ability to work and lead a cross‑functional team in a matrix environment.
Benefits and Rewards 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, and 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 per year (full‑time). The actual salary will be significantly higher, depending on experience, qualifications, and individual competencies.
Commitment To Diversity & Inclusion Novartis is committed to building an outstanding, inclusive working environment and diverse teams, representative of the patients and communities we serve.
Adjustments For Applicants With Disabilities If you require an adjustment during the recruitment process due to a medical condition, physical disability or a neurodiverse condition, please reach out to disabilities.austria@novartis.com and let us know the nature of your request and contact details. We can provide advice on suitable positions and guidance at all stages of the application process. Austrian law allows candidates to involve the local disability representative, Behindertenvertrauensperson (BVP), in the application process. Please inform us in advance if you wish to request this service.
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As a Senior Expert you will be part of a team developing new Biologic drugs. The Analytical Operations team is responsible for releasing the product for clinical trial and investigating the stability behavior of the drugs. We also validate the methods used for release and are responsible for transferring those methods to our commercial organization or external partners.
About The Role Key responsibilities
Independently manage key tasks for projects (e.g., release, stability studies, validation, and transfer activities).
Write protocols, scientific reports, lab procedures and prepare ready‑to‑submit documents for releases or stability documents and transfer reports.
Approve GMP documents and test records; investigate quality events within the project (e.g., deviations, changes, out‑of‑spec events).
Support the lab team in troubleshooting existing methods, processes, or solving higher‑complexity problems within projects.
Essential Requirements
Master’s degree in biotechnology, biochemical engineering, biology, chemistry, biochemistry or a related field with at least 4 years of relevant industry experience, or PhD in a relevant field with 2+ years experience in pharmaceutical industry.
Proficiency in English and German is beneficial.
Good knowledge of pharmaceutical, chemical analytics, QC or equivalent technical and scientific principles.
Proven experience within a GMP environment.
Strong theoretical and scientific knowledge in expertise areas (e.g., HPLC, CE).
Desirable Requirements
Can‑do mindset with strong communication across organizational interfaces and presentation skills.
Ability to work and lead a cross‑functional team in a matrix environment.
Benefits and Rewards 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, and 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 per year (full‑time). The actual salary will be significantly higher, depending on experience, qualifications, and individual competencies.
Commitment To Diversity & Inclusion Novartis is committed to building an outstanding, inclusive working environment and diverse teams, representative of the patients and communities we serve.
Adjustments For Applicants With Disabilities If you require an adjustment during the recruitment process due to a medical condition, physical disability or a neurodiverse condition, please reach out to disabilities.austria@novartis.com and let us know the nature of your request and contact details. We can provide advice on suitable positions and guidance at all stages of the application process. Austrian law allows candidates to involve the local disability representative, Behindertenvertrauensperson (BVP), in the application process. Please inform us in advance if you wish to request this service.
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