Markus Kornprobst

Section Leader, Analytical Development and QC at Roche

Basel, Basel, Switzerland

About

I am a protein biochemist (Dr. rer. nat.) holding a position as Section Leader at Roche (Basel) responsible for analytical development and quality control of biopharmaceuticals during clinical trials (IND) and licensing (BLA/MAA). After studying Molecular Biotechnology at TU München, I did my PhD at the Biochemistry Center of Heidelberg in the field of eukaryotic ribosome biogenesis. Before joining Roche in 2018, I worked as research scientist (drug discovery and validation) for Immuno-Oncology biotech Immunocore Ltd. in Oxfordshire (UK).

Experience

  • Roche (Full-time · 8 yrs 2 mos)
    • Section Leader, Analytical Development and QC (Drug Product)
      Sep 2025 - Present · 10 mos

      - Direct technical and personnel management of a team of approximately 30, ensuring development, training, compliance, workload organization, resource allocation, and continuous improvement. - Mentor and coach teams on early- and late-stage biologics portfolio programs, ensuring efficient project timelines and successful licensing outcomes (IMA). - Drive the development and implementation of new technologies to enhance analytical and operational performance. - Develop and implement strategies and goals aligned with organizational priorities and the needs of product stakeholders.

    • Group Leader - Development Analytics Biochemistry
      May 2018 - Sep 2025 · 7 yrs 5 mos

      Our department within Roche's Pharma division is responsible for biochemical and biophysical Analytical Development, Quality Control and Compliance for Biopharmaceuticals from Investigational New Drug (IND/IMPD) to licensing&Launch (BLA/MAA). Our activities include stability & release testing of drug substance (GMP), in-process control testing, method development & validation, equipment qualification, development of analytical control strategy, (p)CQA assessment, variant characterization, method transfer, analytical comparability assessment, process development & validation and implementation of novel technologies into our method repertoire. Responsibilities/Roles: - Drug Substance (DS) analytical Lead for Early and Late Stage projects - Analytical Tech-Transfer Lead - QbD (Quality by Design) Control Strategy Team Lead for Europe - AET (Analytical Expert Team) member for Charge Heterogeneity methods

  • Scientist - Biochemistry/Protein Engineering (Infectious Diseases) at Immunocore
    Apr 2017 - Mar 2018 · 1 yr

    Immunocore Ltd. is one of the world’s leading T cell receptor (TCR) company developing biological drugs to treat cancer, infectious diseases and autoimmune diseases - utilising their pioneering soluble TCR technology platform. I was working in Immunocore's department of Infectious Diseases (ID), where I was identifying, validating, and engineering suitable immune-activating TCR-based reagents that are subject to preclinical and clinical assessment.

  • PhD in Biochemistry (Center for Biochemistry, Heidelberg) at Ruprecht-Karls-Universität Heidelberg
    Mar 2012 - Feb 2017 · 5 yrs

    Lab of Prof. Dr. Ed Hurt. Title: "Deciphering eukaryotic ribosome biogenesis: Structure and function of the 90S pre-ribosome providing unprecedented insight into the birth of the eukaryotic small ribosomal subunit (40S)". Additional tasks: Supervision of Master's and Bachelor's students.

  • Master's Thesis Student at TU München
    Jan 2011 - Oct 2011 · 10 mos

    Master’s Thesis in eukaryotic Gene Targeting (Module of Molecular Medicine), lab of Prof. Angelika Schnieke. Project: “Pancreas-specific expression of Cre recombinase by successful and efficient targeting of the putative porcine ROSA26 locus”.

  • Protein Engineering Research Internship at TU München
    2010 - 2010 · Less than a year

    2-month Protein Engineering Internship in the team of Prof. Dr. Arne Skerra: “Engineering of a bacterial omega-transaminase for industrial diamine production”.