waypointjobs

Suntra MedTech Solutions

Agile Program Lead / Principal Software Engineer – Medical Device Development

bedford, NH

Check who can apply and the requirements below before continuing.

About this opportunity

Suntra MedTech Solutions lists this Agile Program Lead / Principal Software Engineer – Medical Device Development opportunity in bedford, New Hampshire. Review the employer’s description below for duties, qualifications and application requirements.

Job description

Description

We are accepting resumes for an experienced software engineer operating as a Product Owner / Scrum Master to serve as the connective tissue between technical development teams (software, firmware, systems, cybersecurity, electronics, mechanical, test) and the Program Manager responsible for overall product delivery. This role ensures that requirements are clearly defined, prioritized, and executed using agile practices—while maintaining compliance with medical device regulatory standards.

We are accepting resumes for an experienced software engineer operating as a Product Owner / Scrum Master to serve as the connective tissue between technical development teams (software, firmware, systems, cybersecurity, electronics, mechanical, test) and the Program Manager responsible for overall product delivery. This role ensures that requirements are clearly defined, prioritized, and executed using agile practices—while maintaining compliance with medical device regulatory standards.

The ideal candidate understands both agile product delivery and regulated medical device development and can enable the team to benefit from an agile development process while ensuring that program-level objectives are met.

Responsibilities

Product Ownership & Backlog Management

Own and manage the product backlog, ensuring alignment with program milestones, regulatory requirements, and customer needs

Translate program-level requirements, system requirements, and user needs into clear, well-defined user stories and acceptance criteria

Prioritize backlog items based on risk, regulatory impact, value, and delivery timelines

Ensure traceability between user needs, system/software requirements, implementation, and verification activities

Scrum Master & Agile Execution

Serve as Scrum Master for one or more multi-disciplinary development teams

Facilitate agile ceremonies: backlog grooming, sprint planning, standups, sprint reviews, and retrospectives

Remove impediments and proactively manage dependencies across teams

Coach teams on agile best practices within a regulated development environment

Program & Stakeholder Interface

Act as the primary liaison between the technical team and Program Manager

Ensure development work aligns with program schedules, deliverables, and risk management plans

Communicate progress, risks, and tradeoffs clearly to program leadership and stakeholders

Support cross-functional coordination with Quality, Regulatory Affairs, Clinical, and Cybersecurity teams

Regulatory & Quality Alignment

Ensure agile artifacts support design controls, including documentation, traceability, and verification planning

Work within ISO 13485, IEC 62304, IEC 62366, and FDA design control requirements

Partner with Quality and Regulatory teams to ensure backlog items and increments are audit-ready

Support cybersecurity, safety, and risk management activities as part of product development

Requirements

Required Qualifications

Bachelor’s Degree and 5+ years industry experience, with 2+ years in product ownership, scrum mastery, or technical program delivery

Hybrid environment but must be flexible and willing to work onsite for a minimum of 3 days per week

Experience working in medical device or other regulated product development environments

Strong understanding of Agile/Scrum frameworks and practical application in regulated settings

Ability to translate complex technical and regulatory requirements into actionable development work

Excellent communication skills across technical, quality, and executive stakeholders

Experience with development of software, firmware, or connected medical devices

Preferred Qualifications

Familiarity with FDA submissions (510(k), De Novo, PMA) and design history files (DHF)

Knowledge of cybersecurity for medical devices and secure product development

Experience working closely with Program Managers on multi-disciplinary development programs

Certified Scrum Master (CSM), SAFe, or Product Owner certification

#J-18808-Ljbffr

Worksite address

bedford, NH, 03110, US

Who can apply

Review the original listing for work authorization, qualifications and employer requirements.

Ready for your next step?Apply on the official website
Apply on WhatJobs ↗

Explore related searches

Current related jobs