What are the responsibilities and job description for the US_East | Agile Scrum Master_L3 position at Expedite Technology Solutions LLC?
Need R2D2 # 1MTWLY
Possible 3 Month CTH | No Fees | Do Not Re-Post | Confidential
Submit candidates under their legal name and use only *** template
Important Information
Role: Senior Scrum Master (SAFe/Agile/Scrum) Medical Devices
Work Location: Lakewood, Colorado
Please send it with this information
Legal Name
Location (City and State):
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Rate
Availability:
Phone #:
Mobile#:
Email Address
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Hiring Status
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Job Description
"Foster collaboration, transparency, and continuous improvement within teams.
"Coach Product Owners and stakeholders in backlog management and Agile principles.
"Promote a culture of innovation and servant leadership.
Scrum/SAFe Execution
"Facilitate Scrum ceremonies (Daily Standups, Sprint Planning, Sprint Reviews, and Retrospectives).
"Remove impediments/blockers that hinder team progress.
"Track and report Agile metrics (velocity, burn-down charts, lead time, cycle time, etc.) to assess team performance.
"Drive Program Increment (PI) planning, ART syncs, and SAFe Release Train events in alignment with SAFe principles.
Regulatory & Compliance Alignment
"Ensure Agile development processes align with medical device regulations (e.g., FDA 21 CFR Part 820, ISO 13485, IEC 62304).
"Support documentation and traceability requirements for Design Control & Risk Management.
"Collaborate with Quality & Regulatory teams to maintain compliance in an Agile environment.
Cross-functional Collaboration
"Work closely with R&D, Quality Assurance, Regulatory, Software Development, and Product Management teams.
"Align Agile processes with risk management, cybersecurity, and validation requirements in medical device development.
"Support hardware-software integration and cross-team coordination.
"Medical device industry experience with knowledge of FDA/ISO regulations.
"Expertise in SAFe (Scaled Agile Framework) and ability to coach ART (Agile Release Trains).
"Strong understanding of software development life cycle (SDLC) in regulated industries.
"Proficiency in Agile tools (JIRA, Rally, VersionOne, Azure DevOps).
"Excellent facilitation, communication, and conflict resolution skills.
Soemia Pineda
SubCo Staffing Center
Possible 3 Month CTH | No Fees | Do Not Re-Post | Confidential
Submit candidates under their legal name and use only *** template
Important Information
Role: Senior Scrum Master (SAFe/Agile/Scrum) Medical Devices
Work Location: Lakewood, Colorado
Please send it with this information
Legal Name
Location (City and State):
Relocate?
Rate
Availability:
Phone #:
Mobile#:
Email Address
Visa type:
Hiring Status
If the resource has a visa, what company owns it?
Are you working directly with the contractors visa holder?
Job Description
- We are seeking a highly motivated Scrum Master with expertise in SAFe, Agile, and Scrum methodologies, specifically within the medical device industry. The ideal candidate will facilitate Agile practices, coach cross-functional teams, and ensure compliance with regulatory standards (e.g., FDA, ISO 13485, IEC 62304) while driving high-quality product development.
- Agile Facilitation & Coaching
"Foster collaboration, transparency, and continuous improvement within teams.
"Coach Product Owners and stakeholders in backlog management and Agile principles.
"Promote a culture of innovation and servant leadership.
Scrum/SAFe Execution
"Facilitate Scrum ceremonies (Daily Standups, Sprint Planning, Sprint Reviews, and Retrospectives).
"Remove impediments/blockers that hinder team progress.
"Track and report Agile metrics (velocity, burn-down charts, lead time, cycle time, etc.) to assess team performance.
"Drive Program Increment (PI) planning, ART syncs, and SAFe Release Train events in alignment with SAFe principles.
Regulatory & Compliance Alignment
"Ensure Agile development processes align with medical device regulations (e.g., FDA 21 CFR Part 820, ISO 13485, IEC 62304).
"Support documentation and traceability requirements for Design Control & Risk Management.
"Collaborate with Quality & Regulatory teams to maintain compliance in an Agile environment.
Cross-functional Collaboration
"Work closely with R&D, Quality Assurance, Regulatory, Software Development, and Product Management teams.
"Align Agile processes with risk management, cybersecurity, and validation requirements in medical device development.
"Support hardware-software integration and cross-team coordination.
- Required
"Medical device industry experience with knowledge of FDA/ISO regulations.
"Expertise in SAFe (Scaled Agile Framework) and ability to coach ART (Agile Release Trains).
"Strong understanding of software development life cycle (SDLC) in regulated industries.
"Proficiency in Agile tools (JIRA, Rally, VersionOne, Azure DevOps).
"Excellent facilitation, communication, and conflict resolution skills.
Soemia Pineda
SubCo Staffing Center
- North America
