Job description

Description Note: GlobalLogic estimates the starting pay range for this role to be performed remote in USA is $140,000 – $150,000 and reflects base salary only. This pay range is provided as a good faith estimate and the amount offered may be higher or lower. GlobalLogic takes many factors into consideration in making an offer, including candidate qualifications, work experience, operational needs, travel and onsite requirements, internal peer equity, prevailing wage, responsibilities, and other market and business considerations. Job Title: Product Owner Location: Remote Join the Engineering team delivering safety-critical, regulated mobile software for diabetes care. You will focus on product quality and reliability for international markets, with domain onboarding provided to accelerate your impact. Framework development is out of scope for this role; you will use and configure the existing internal framework to achieve high coverage and reliable automation. Requirements Minimum Requirements: Bachelor’s degree + 3 or more years of relevant experience (or 8+ years of experience without a degree). Experience in Medical Device development or highly regulated products. Agile/SAFe methodologies in a Product Owner role. Knowledge of embedded software, firmware, and hardware development. Domain Expertise: Demonstrated experience working as a Product Owner within the MedTech / Medical Device industry. Regulated Delivery Experience: Hands-on experience with regulated software delivery, including documenting changes for medical device compliance (design docs, risk assessments, and SRSs). Technical Capability: Experience in Android mobile application development and device connectivity, specifically related to Pod OTA and Pod Communication features.Strong communication skills across technical and non-technical audiences. Preferred Skills: Experience with diabetes technology products. Mobile Application or Cloud development background. Proactive stakeholder communication. Understanding of medical device regulations and standards (e.g. ISO 13485, IEC 62304, ISO 14971, EU MDR) will be a huge plus Experience in FDA Pre-Submissions, FDA clearance, PCCP Framework Knowledge will be a plus Familiarity with UI/UX principles and experience collaborating with UX/UI design teams Detail-oriented with strong written and verbal skills. Job responsibilities Backlog Ownership: Own and manage the product backlog for the Android application, specifically for Pod OTA and related Pod Communication features. User Stories & Acceptance Criteria: Write clear, detailed user stories and acceptance criteria to ensure engineering teams understand what to build and how to test it. Cross-Functional Collaboration: Partner closely across teams, including Engineering, QA, Regulatory, and Hardware/Firmware groups. Release Planning: Actively assist with and support release planning efforts. Medical Device Compliance: Ensure all changes and modifications are thoroughly documented to meet medical device compliance standards, including design documentation and risk assessments. QA & Test Case Definition: Assist QA in defining test cases for real-world scenarios in connection with Acceptance Criteria and Software Requirement Specifications (SRSs). What we offer Exciting Projects: Come take your place at the forefront of digital transformation! With clients across all industries and sectors, we offer an opportunity to work on market-defining products using the latest technologies. Collaborative Environment: You can expand your skills by collaborating with a diverse team of highly talented people in an open, laidback environment — or even abroad in one of our global centers or client facilities! Work-Life Balance: GlobalLogic prioritizes work-life balance, which is why we offer flexible work schedules and opportunities to work from home. Professional Development: We provide continuing education classes, professional certification and training (technical, soft skills, language, and communication skills) to help you realize your professional goals. Being part of a global organization, there are additional learning opportunities through international knowledge exchanges. Excellent Benefits: We provide our employees with competitive salaries, health and life insurance, short-term and long-term disability insurance, a matched contribution 401K plan, flexible spending accounts, and PTO and holidays About GlobalLogic GlobalLogic, a Hitachi Group Company, is a trusted digital engineering partner to the world’s largest and most forward-thinking companies. Since 2000, we’ve been at the forefront of the digital revolution – helping create some of the most innovative and widely used digital products and experiences. Today we continue to collaborate with clients in transforming businesses and redefining industries through intelligent products, platforms, and services.

Requirements

Must-haves

Job Title: Product Owner
Location: Remote
Bachelor’s degree + 3 or more years of relevant experience (or 8+ years of experience without a degree).
Experience in Medical Device development or highly regulated products.
Agile/SAFe methodologies in a Product Owner role.
Knowledge of embedded software, firmware, and hardware development.
Domain Expertise: Demonstrated experience working as a Product Owner within the MedTech / Medical Device industry.
Regulated Delivery Experience: Hands-on experience with regulated software delivery, including documenting changes for medical device compliance (design docs, risk assessments, and SRSs).
Backlog Ownership: Own and manage the product backlog for the Android application, specifically for Pod OTA and related Pod Communication features.
User Stories & Acceptance Criteria: Write clear, detailed user stories and acceptance criteria to ensure engineering teams understand what to build and how to test it.
Cross-Functional Collaboration: Partner closely across teams, including Engineering, QA, Regulatory, and Hardware/Firmware groups.
Release Planning: Actively assist with and support release planning efforts.
Medical Device Compliance: Ensure all changes and modifications are thoroughly documented to meet medical device compliance standards, including design documentation and risk assessments.
QA & Test Case Definition: Assist QA in defining test cases for real-world scenarios in connection with Acceptance Criteria and Software Requirement Specifications (SRSs).

Nice-to-haves

Experience with diabetes technology products.
Mobile Application or Cloud development background.
Proactive stakeholder communication.
Understanding of medical device regulations and standards (e.g. ISO 13485, IEC 62304, ISO 14971, EU MDR) will be a huge plus
Experience in FDA Pre-Submissions, FDA clearance, PCCP Framework Knowledge will be a plus
Familiarity with UI/UX principles and experience collaborating with UX/UI design teams
Detail-oriented with strong written and verbal skills.

Application prep

Use the role’s language and application details while tailoring your materials.

Keywords to mirror

agile

Platform: globallogic
Effort: medium

Benefits

Benefits detected in the listing.

401k

Pto

Professional Development