Related skills
biotech genai pharma regulatory compliance audit_trailπ Description
- Design and ship production systems around models for research, clinical, and operations.
- Translate workflow needs into hypothesis-driven requirements and plans with endpoints.
- Define launch criteria for regulated contexts with validation evidence and audit readiness.
- Build data environments with auditability, validation, and access controls.
- Run evaluation loops to measure model and system quality against benchmarks.
- Distill deployment learnings into reference architectures and validation templates.
π― Requirements
- 5+ years in software/ML engineering with customer ownership in biotech/pharma.
- Owned customer GenAI deployments end-to-end with evaluation design and evidence generation.
- Delivered AI systems in trial design or scientific operations with validation and compliance.
- Communicate clearly across scientific, clinical, model research, technical, and executive audiences with credibility.
- Apply systems thinking to turn failures and audit findings into repeatable deployment playbooks.
π Benefits
- Hybrid work model: 3 days in the office per week
- Relocation assistance
- Travel up to 50% required
π Relocation support
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