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Job Description
Release Train Engineer (RTE) Pharma / Life Sciences (SAFe)
Role Summary
Datavid provides enterprise-ready software solutions designed to help businesses extract, enrich, and utilize their most valuable knowledge. Our focus is on delivering cutting-edge data engineering and AI services to global enterprises leading in research, development, customer experience, and innovation. With a dedicated team of over 120+ professionals, including software developers, data engineers, machine learning specialists, AI engineers and project managers, Datavid is committed to helping organizations unlock the full potential of their data.
Role Description
We are seeking a SAFe Release Train Engineer (RTE) to join our global engineering team. This is a full-time remote role responsible for facilitating and enabling one or more Agile Release Trains (ARTs) delivering pharmaceutical R&D, clinical, regulatory, quality, or commercial technology capabilities within a regulated life-sciences environment.
The RTE ensures alignment, predictable delivery, and continuous improvement across multiple agile teams while maintaining compliance with GxP, validation, data integrity, and quality standards. The role works closely with Product Management, Architecture, Quality, Regulatory, and senior business stakeholders to enable Lean-Agile delivery at scale without compromising patient safety or regulatory obligations.
Key Responsibilities
Agile Release Train Leadership (Pharma Context)
Act as chief facilitator and servant leader for an Agile Release Train supporting pharma domains such as:
Discovery & Pre-Clinical
Clinical Development & Operations
Regulatory Affairs & Submissions
Pharmacovigilance & Safety
Manufacturing, Quality, or Commercial IT
Establish and sustain ART cadence while respecting regulated delivery constraints
Promote a culture of transparency, quality, and continuous improvement
Program Increment (PI) Planning & Execution
Plan and facilitate PI Planning events involving cross-functional teams, vendors, and business SMEs
Ensure alignment to:
Portfolio themes and roadmap commitments
Regulatory milestones (e.g. submissions, inspections, audits)
Data integrity and validation needs
Facilitate dependency mapping, risk identification, and ROAMing with regulatory and quality awareness
Support PI objective definition and confidence voting in complex stakeholder environments
Facilitation of SAFe Ceremonies
Facilitate and improve ART-level ceremonies:
Scrum of Scrums
PO Sync
System Demos (with validated artefacts where required)
Inspect & Adapt workshops
Ensure ceremonies focus on outcomes, quality, and compliance, not just speed
Dependency, Risk & Impediment Management
Proactively manage cross-team and cross-vendor dependencies involving:
Validation & CSV
Quality Assurance
Regulatory Affairs
Security & Data Privacy
Identify and remove system-level impediments impacting delivery timelines or compliance
Escalate risks appropriately while enabling teams to resolve issues at the lowest possible level
Compliance, Quality & Governance Enablement
Partner with Quality, Validation, and Regulatory teams to:
Embed compliance into agile ways of working
Ensure audit-ready delivery processes
Support documentation, traceability, and evidence generation
Enable agile delivery within GxP-regulated environments without reverting to waterfall behaviours
Coaching & Continuous Improvement
Coach Scrum Masters, Product Owners, and teams on:
SAFe practices adapted for life-sciences delivery
Flow, WIP limits, and value-based prioritisation
Balancing speed with quality and compliance
Drive continuous improvement actions from Inspect & Adapt workshops
Metrics & Transparency
Track and communicate ART-level metrics including:
PI predictability
Flow metrics (Flow Velocity, Flow Time, Flow Load)
Quality and stability indicators where applicable
Provide clear, data-driven updates to senior stakeholders and governance forums
Key Stakeholders
Product Management & Product Owners
Clinical, Regulatory, Safety, and Quality stakeholders
Architecture, Platform, and DevOps teams
Validation & Compliance functions
External vendors and systems integrators
Portfolio and Digital Transformation leadership
Required Experience & Skills
7+ years experience in Agile delivery roles (Senior Scrum Master, Agile Coach, Program/Delivery Manager)
Proven experience as an RTE or equivalent role within pharma or life sciences
Strong understanding of SAFe and Agile at scale
Experience operating in GxP-regulated environments
Ability to facilitate large, complex planning and alignment events
Strong stakeholder management skills in matrixed organisations
Calm, structured approach to ambiguity and regulatory complexity
Preferred Experience
Exposure to clinical systems (CTMS, EDC, eTMF, Safety systems)
Experience supporting regulatory submissions or inspections
Working knowledge of CSV, validation, and audit requirements
Experience coordinating multiple vendors or global delivery teams
Certifications (Preferred)
SAFe Release Train Engineer (RTE)
SAFe Agilist (SA)
Scrum Master / Advanced Scrum Master
Life-sciences or GxP training / certification (advantageous)
Job ID: 136633089