Technical Product Manager (all genders)

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Collaborating closely with software engineering teams on architecture trade-offs, APIs, databases, data flows, integrations, environments, testing strategies, defect triage, CI/CD implications and release preparation.

Partnering with data science teams on model lifecycle topics such as data pipelines, model versioning, spectral databases, QA Scan workflows, residual and outlier monitoring, model limitations and retraining triggers.

Partnering with QM/QA teams on regulated software requirements including traceability, audit trail expectations, role‑based access control, change management, validation evidence and release documentation.

Supporting sales, service and marketing teams with accurate product knowledge — including clear communication of current software capabilities, limitations, available proof points and realistic expectations.

Creating sustainable operating documentation to ensure product and workflow knowledge is scalable and not dependent on individual team members.

You have a strong technical understanding of modern software development processes, including requirements engineering, user stories, acceptance criteria, APIs, databases, environments, testing, versioning, release management, defect handling and developer collaboration. You have experience working with agile software teams.

You have strong stakeholder management skills and enjoy collaborating across software engineering, data science, application science, quality, service, sales, marketing and customer teams.

Benefits Company pension scheme 300 EUR Feel‑Free Health Budget per year Kindergarten allowance up to 180 EUR per month Monthly internet allowance Vouchers worth 20 EUR per month Bike leasing Electronics leasing Car subscription model Attractive bonus model #J-18808-Ljbffr Technical Product Manager: Bioanalytics Software & Infrastructure Location: Germany Hybrid: Esslingen am Neckar / remote by agreement Full-time Level: Experienced individual contributor You will be...

Owning technical product requirements and ensuring backlog quality for CLADE’s bioanalytics software workflows, especially Sphere, QA Scan, SpecHub/data workflows and MIRA-connected software capabilities.

Translating scientific workflows, user needs, software and deployment constraints, as well as quality requirements into clear user stories, acceptance criteria, release notes and handover documentation.

Coordinating product input for ART/PI planning, sprint and iteration planning, backlog refinement, dependency mapping and de‑scoping recommendations.

Understanding and documenting customer infrastructure requirements, including on‑premise deployments, cloud access, data residency, network and security constraints, server environments, user access management, backups, monitoring, update processes and supportability.

Working closely with application science and domain experts to understand sample types, analytical methods, workflow constraints, method performance, customer use cases and scientific validation needs.

Must‑have You have 3–6+ years of experience in technical product management, product ownership, solution engineering, software product coordination, scientific software delivery or a similar role within complex B2B software environments.

You bring a solid understanding of infrastructure and data‑center topics such as cloud and on‑premise environments, servers, virtual machines or containers, networking fundamentals, firewalls/VPNs, identity and access management, logging, monitoring, backups, disaster recovery, patching, supportability and data residency requirements.

You have scientific knowledge through education or professional experience in life sciences, biotechnology, chemistry, biochemistry, bioprocess engineering, pharmaceutical sciences, analytical chemistry, spectroscopy, chemometrics, pharmaceutical QC or analytical development.

You are able to understand biopharma workflows and translate scientific requirements into product, software, data and documentation requirements. Experience with SAFe, Agile Release Trains, PI planning or comparable scaled delivery frameworks is a plus.

You are skilled at creating clear technical documentation, decision logs, release notes, support handovers, workflow maps and stakeholder‑ready summaries. You are fluent in English. German is strongly preferred and may be required depending on the day‑to‑day internal communication setup.

Strong plus You have hands‑on exposure to FTIR/MIR spectroscopy, spectral data, chemometric models, analytical method development or laboratory automation. You have experience working in regulated or quality‑sensitive environments such as GMP, GLP, ISO, pharmaceutical manufacturing, diagnostics, medtech, 21 CFR Part 11, EU Annex 11, CSV or GAMP 5.

You are familiar with LIMS, ELN, QMS, ERP integrations, OPC UA, REST APIs, analytical instruments, scientific data platforms or laboratory automation systems.

You understand biologics workflows such as formulation, buffer QC, UF/DF, upstream/downstream processing, raw material testing, release testing, PS20/PS80, mAbs, ADCs, peptides, mRNA or gene therapy. You have hands‑on experience in startup or scale‑up environments where product roles need to stay pragmatic, execution‑oriented and adaptable.