Jobs at Enveda Biosciences

As a Senior Research Associate in In Vivo Pharmacology, you'll conduct efficacy studies, develop disease models, analyze data, and collaborate on innovative therapeutics.

Design, build, and maintain scalable data engineering infrastructure on Databricks and Azure. Implement CI/CD, IaC (Pulumi), monitoring, and automation. Collaborate with data scientists and platform teams, improve security and observability, mentor junior engineers, and maintain documentation and internal tooling.

Coordinate end-to-end procurement for a biopharma research site: source and evaluate vendors, manage RFQs, create PRs/POs in ERP, track deliveries, maintain inventory records and reconciliation, support customs/logistics, and produce procurement and inventory reports while driving continuous improvement.

Operate and maintain LC-MS/MS and HPLC instrumentation; develop, optimize, and validate quantitative bioanalytical methods for small molecules; perform sample processing and execute DMPK-focused workflows; analyze and interpret data in compliance with regulatory and scientific standards.

Lead DMPK, clinical pharmacology, and quantitative pharmacology (PK/PD, modeling & simulation) across discovery and development. Drive clinical pharmacology strategy, design and interpret PK/PD studies, support regulatory submissions (IND/NDA/BLA), represent the company with health authorities, manage CRO and cross-functional collaborations, and provide scientific leadership for advancing small-molecule candidates from nomination through clinical development.

The Software Engineer will architect and deliver systems that automate scientific workflows, build solutions with Vue, Python, Databricks, and Azure, and design integrations for data flow efficiency.

Lead global regulatory strategy for small molecules and combination products across development stages. Oversee interactions with FDA, EMA and other agencies; author and submit INDs, CTAs, briefing books, and response packages. Build and manage a high-performing regulatory team covering strategy, operations, and publishing to enable successful regulatory submissions and program advancement.