Senior Analytical Scientist-Biologics Evidence Lab (all genders)

Do we belong together?

CLADE builds analytical technologies for biopharma teams that need faster, simpler and more data-rich ways to characterise complex liquid samples.

We are building the MIRA Evidence Lab to generate the scientific proof behind our product claims, customer workflows and product roadmap.

This is not a routine QC role.

It is a senior scientific role for someone who can design experiments, analyse data, compare MIRA against reference methods and turn results into evidence that Product, Data Science, Commercial and customers can trust.

You will work at the interface of biologics analytics, spectroscopy, chemometrics and experimental design.

You will be...

• Leading high-value evidence studies from initial scientific question through to final reporting.
• Designing experimental protocols, Do Es, sample matrices, controls, as well as robustness, stress, and comparator studies for priority MIRA workflows.
• Planning and analysing studies in biologics applications, including formulation analytics, excipient quantification, polysorbate analysis, protein concentration and structure, UF/DF, as well as stability and release-like workflows.
• Evaluating MIRA results against orthogonal and reference methods such as HPLC/UPLC, UV-Vis (A280), CD, p H/osmolality, CE, DLS/MALS, LC-MS, and external laboratory data.
• Analysing MIR/FTIR spectral and reference data to assess performance, reproducibility, robustness, uncertainty, and method limitations.
• Collaborating closely with Product and Data Science teams to translate evidence into improvements in instruments, software, models, and workflows.
• Preparing high-quality documentation, including protocols, study reports, evidence packages, application notes, technical notes, SOPs, and claim-support materials.
• Supporting customer-proof activities for validated workflows while maintaining a focused, evidence-driven intake approach.
• Coordinating external reference analytics when required.
• Contributing to the development of a scalable lab operating model ensuring every major claim is backed by defined protocols, reports, reference methods, and clearly stated limitations.

You're a good fit for us if...

• You bring solid experience in pharma or biologics, which is essential for this role.
• You have several years of industry experience in pharma, biotech, CDMO, or related areas such as analytical development, QC, process analytics, formulation development, or biologics characterisation.
• You have hands-on experience working with biological or biopharmaceutical samples, including proteins, monoclonal antibodies (m Abs), bispecifics, ADCs, peptides, AAV/p DNA, or formulated drug products.
• You possess a strong understanding of analytical method development, including qualification, validation, transfer, troubleshooting, and documentation.
• You are able to independently design experiments, including defining sample matrices, controls, replicates, acceptance criteria, and statistical analysis plans.
• You have strong data analysis skills and can clearly interpret and communicate complex experimental results.
• You are familiar with GMP/Gx P environments, including data integrity principles, SOPs, change control processes, deviations, and ICH-style approaches to analytical development and validation.
• You demonstrate excellent scientific writing skills in English.
• You hold a degree in analytical chemistry, biochemistry, biotechnology, pharmaceutical sciences, biophysics, or a related field; a Ph D is preferred, though an MSc with strong and relevant industry experience is equally valued.

Nice to have

• Experience with MIR/FTIR, NIR, Raman, UV-Vis, CD, fluorescence or other spectroscopic techniques.
• Experience with chemometrics or multivariate analysis, such as PCA, PLS, calibration, preprocessing, model transfer and outlier analysis.
• Experience with biologics analytical methods such as SEC, IEX, RP-HPLC/UPLC, CE-SDS, c IEF, LC-MS, DLS, MALS, ELISA, A280, p H, osmolality, or surfactant and excipient assays.
• Experience with Python, R, JMP, MATLAB, Graph Pad Prism or similar analysis tools.
• Experience with external reference labs, CROs, CDMOs or customer-facing technical projects.
• Experience with high-throughput analytics, autosamplers, LIMS/ELN or automated sample workflows.
• Scientific communication experience with customers, product teams or commercial teams.
• That´s CLADE

Our colleagues are bold, enabling, versatile and genuine.

We support each other, dare to question ourselves and the status quo and we stay true to ourselves.

If you find yourself in these values, then read to the end and get in touch with us directly.

• What makes us unique
• If you live near one of our offices and want to work locally, you always have a place to work, but you can also work mobile within Germany and Europe (up to 60 days per year).
• Our company consists of motivated, passionate and open-minded people with a great drive who want to develop together with you.
• Our in-house processes are sophisticated, unbureaucratic and simple and we are big fans of short decision-making paths.
• Your onboarding is important to us, so you donree worry about anything in the first week, you get insights into all relevant topics.
• We offer a company pension scheme, a 300 EUR - Feel Free Health Budget per year, a kindergarten allowance of up to 180 EUR per month, a monthly internet allowance, vouchers worth 20 EUR per month, bike leasing, electronics leasing subscription model and an attractive bonus model.
• We live and love diversity, inclusion and internationality.
• CLADEtivities: regular company-wide and site-specific events await you.
• Opportunity to participate in various committees and working groups.

If you have any questions about the position or the company, you can contact our people & culture team at any time at

If you want to learn more about us and our values, visit our homepage ( our Linked In channel ( or Instagram channel (@peopleatclade).

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