29.10.2026 aktualisiert

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Applied AI & MLOps Engineer | Statistical Geneticist | Biomedical ML Specialist

Mössingen, Deutschland
Weltweit
PhD in Genetic Epidemiology, University of Pune (2014)
Mössingen, Deutschland
Weltweit
PhD in Genetic Epidemiology, University of Pune (2014)

Profilanlagen

CV_Sandeep_Grover.pdf

Über mich

Applied AI, MLOps & Biostatistik (PhD, 13+ J.): Python, GenAI, RAG, LangGraph, Risikomodellierung, Confounder-Analysen & Multi-Omics (>150k Kohorten, 72 Publikationen). Deutsch B1, Englisch C2, deutsche Staatsangehörigkeit, verfügbar ab 01.11.2026.

Skills

Data Integration
AI Engineering & Multi-Agent Orchestration
Expertise in context engineering, multi-LLM and multi-agent orchestration, RAG, reranking and evaluation. Proficiency with LangChain, ChromaDB, PyTorch, scikit-learn, Python, R, Bash and SQL for building and operating production AI systems with claim-level provenance.

MLOps & DevOps
Hands-on experience with MLflow, DVC, Docker, Kubernetes, Airflow, Git/GitHub Actions, Prometheus, Grafana, model serving and drift monitoring, as well as HPC/SLURM, Snakemake and Nextflow for workflow orchestration across local and cloud compute environments.

Statistical Genetics & Biomedical Science
Deep knowledge of GWAS, Mendelian randomisation, HLA, fine mapping (SuSiE), colocalisation, eQTL/pQTL/sQTL, MR-PheWAS, PLINK, SAIGE and REGENIE, as well as RNA-seq, single-cell and multi-omics integration for biomedical research.

Research Automation & Reproducible Analysis
Building multi-step AI workflows for evidence synthesis and reproducible analysis, with every claim traced to its source, including biomedical evidence retrieval, reference verification, clinical-document extraction and manuscript consistency checks.

Genomics & Causal Inference
Bidirectional and multivariable Mendelian randomisation, gene-burden testing and multi-omics interpretation; SNP-array/WGS concordance and QC; reproducible GATK/hap.py variant-calling benchmarking.

Clinical & Epidemiological Research
Reanalysis of surgical, perioperative, patient-education and EEG studies using statistical and ML methods; addressing confounding, survival outcomes and missing data with sensitivity analyses and reproducible figures.

Scientific Writing & International Collaboration
First- and joint first-author publications in high-impact journals including Gut, Neurology and Movement Disorders. Collaboration with scientists and clinicians across countries on analysis, interpretation and revision.

Teaching & Knowledge Transfer
Teaching Applied Multiple Regression for students of Mathematik in Medizin und Lebenswissenschaften; creating reproducible code walkthroughs and automated narrated video lectures in scientific computing and AI.

Spatial & Single-Cell Transcriptomics
Training in spatial transcriptomics, single-cell transcriptomics in R, multi-omics data integration and biology-informed visualisation through SIB Swiss Institute of Bioinformatics (2026).

Protein Structure Prediction & Long-Read Sequencing
Familiarity with AlphaFold for protein structure prediction and long-read and Nanopore direct-RNA sequencing as part of advanced bioinformatics development.

Erfahrung

Berufserfahrungmehr als 10 Jahre
Freelancer seit2019

Sprachen

DeutschGrundkenntnisseEnglischverhandlungssicher

Projekthistorie

Freelance Independent Research Consultant

Independent Research Consultant: Biomedical Science & AI Engineering
Coordinates AI agents and multiple cloud and local LLMs; builds multi-step AI workflows for evidence synthesis and reproducible analysis; builds multimodal text/image models with experiment tracking and a model registry; conducts genomics and causal inference studies; delivers manuscript projects spanning neurology, anaesthesiology, oncology, infectious disease and genomics; collaborates internationally and creates reproducible code walkthroughs and automated narrated video lectures.

Research Scientist (Wissenschaftlicher Mitarbeiter), Bioinformatics and Biostatistics

Institut fur Humangenetik, Philipps-Universitat Marburg
Conducted multi-omics and causal-inference studies of immune-mediated and neurological diseases; first author of the first GWAS of idiopathic achalasia and led the first GWAS of lymphatic filariasis in a West African population; integrated HLA imputation, fine mapping (SuSiE) and eQTL evidence; contributed to aortic-stenosis GWAS; mentored PhD students.

Research Scientist (Wissenschaftlicher Mitarbeiter), Genetic Epidemiology

Institut fur Klinische Epidemiologie und Angewandte Biometrie, Universitatsklinikum Tubingen
Conducted genome-wide analyses for the international COURAGE-PD consortium; first author of its age-at-onset GWAS meta-analysis (Neurology, 2022) and joint first-author SV2C locus replication (Movement Disorders, 2021); developed reproducible multi-cohort analysis workflows and harmonised genetic data with international collaborators.

Research Scientist (Wissenschaftlicher Mitarbeiter), Biostatistics

Institut fur Medizinische Biometrie und Statistik (IMBS), Universitat zu Lubeck
Developed statistical-genetics and causal-inference workflows for DFG/BMBF-funded projects; first-author Mendelian-randomisation study of risky behaviours and Parkinson disease (Neurology, 2019) and methods chapter (2017); taught Applied Multiple Regression and supported supervision of internship and BSc theses.

Research Scientist (Wissenschaftlicher Mitarbeiter), Epidemiology

Charite University Medical Center, Berlin
Analysed paediatric influenza surveillance data using regression and predictive analyses of the surveillance research database; co-author of an influenza-testing evaluation (PLoS One, 2014).

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