Requirements Engineer Lead

CooperCompanies•Trumbull, CT

2d•Onsite

About The Position

The Research and Development Digital Innovation team within CooperSurgical leads efforts to translate user needs into product solutions and define and document product development requirements. The Requirements Engineer Lead is a leadership role that will be responsible for both leading product development and championing best practices in requirements management, business analysis, and technical product ownership. She/He will work cross-functionally to ensure Cooper delivers user-centric and cutting-edge solutions in Fertility and Woman’s Health spaces. As a Requirements Engineer Lead, you will work on product definition of software solutions both as stand-alone applications and as part of system solutions. You will be responsible for ensuring that functional and non-functional requirements meet user and business needs. You will work to support entire product development life cycle from product ideation through product development and launch.

Requirements

At least 8 years of experience as a Requirements Engineer or Technical Product Owner for Agile teams in Software Development environment.
Ability to define customer journeys, understand user needs, and ensure requirements deliver meaningful user value.
Ability to translate business needs into technical requirements and align diverse stakeholders (business, engineering, UX, QA).
Proven ability to elicit, analyze, document, and validate functional and non-functional requirements (e.g., user stories, use cases, acceptance criteria).
Hands-on experience prioritizing backlogs, defining MVP scope, and working closely with cross-functional Agile teams.
Strong technical background with good understanding of software development methodologies, solution architecture and cloud technologies.
Proficiency in tools like Jira, Confluence, Azure DevOps, or similar for backlog management and documentation.
Experience creating and managing traceability matrices (RTM) linking requirements to design, risk controls, verification, and validation activities.
Understanding of embedded systems, SaMD (Software as a Medical Device), interoperability (HL7, FHIR), and data integrity requirements.
Familiarity with FDA regulations (21 CFR Part 820), ISO 13485, IEC 62304, HIPAA, and software validation requirements in regulated healthcare environments.
Ability to lead without authority, facilitate workshops, and drive consensus across technical and business teams.
Excellent verbal and written communication skills with the ability to articulate complex technical concepts to both technical and non-technical stakeholders.
An outcome focused and detail-oriented mindset, including process discipline and drive for timely project completion.

Nice To Haves

Master’s degree preferred

Responsibilities

In collaboration with users and product marketing, work to understand user needs and business objectives.
Conduct analysis of user journeys, workflows, and use cases.
Translate user needs into product requirements, epics, user stories, and acceptance criteria for development sprints.
Work with development and testing teams to ensure user stories and acceptance criteria are clearly understood.
Work with UI/UX leads to support translation of requirements into visual and interactive design assets.
Document, manage and prioritize product backlog, ensuring alignment with evolving requirements and business goals.
Foster cross-functional collaboration to ensure alignment on technical requirements, timelines, and priorities.
Actively participate in agile meetings to maintain transparency on progress, impediments, and successes.
Own and maintain comprehensive product documentation, including user guides, and release notes.
Champion best practices involved in requirements engineering and technical product ownership.