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QA Software Testing Manager

Medpace Holdings

Listing collected from Medpace Holdings's career site. NextChapter is independent of Medpace Holdings.

Cincinnati, OH · Posted November 3, 2026

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About the job

Our corporate activities are growing rapidly, and we are currently seeking a full-time Software Testing Manager to join our Information Technology team. This position will manage a team of software testing engineers and software validation projects to implement effective and high quality software solutions. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you!

Responsibilities

Lead validation staff in developing, coordinating, and maintaining full SDLC validation deliverables for Medpace regulated software applications, including Validation & Test Plans, User Requirements & Functional Specifications, Functional & User Acceptance Testing, Traceability Matrices, and Validation Summary Reports;

Coordinate and assign systems and projects to validation staff according to priorities, timelines and availability;

Maintain oversight of validation staff in managing change control of Medpace software applications;

Ensure compliance of Medpace computer systems with GxP and SOx regulatory requirements;

Ensure compliance of system validation Standard Operating Procedures (SOPs) with regulatory requirements;

Ensure consistency of systems validation SOPs with best practices of industry;

Lead validation team in implementing tools and procedures to facilitate validation and documentation activities; and

Participate in Sponsor audits;

Qualifications

Bachelor's Degree;

7+ years of experience in SDLC, testing, and validation, preferably in an Agile environment and/or regulated industry;

Advanced knowledge of software development life cycle;

Knowledge and understanding of the application of Risk Management concepts;

Excellent analytical, written, and oral communication skills;

Previous supervisory experience is preferred; and

Experience in the regulated healthcare industry, with working knowledge of Good Clinical Practice and 21 CFR Part 11, is a plus!

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.

Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

Office based environment with on-site mentors

Defined career paths with clear advancement opportunities

Industry renowned onboarding and training programs designed to accelerate professional development

Ongoing training and continuous learning opportunities throughout your career

An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

Competitive compensation programs that recognize and reward performance

Comprehensive health, wellness, retirement, and PTO benefits

Office based culture with occasional WFH that provides flexibility for eligible positions after training

Company-sponsored social events and intramural sports

Cincinnati Headquarters Experience

A modern corporate campus designed to support collaboration and productivity

Multiple on-site dining options in the heart of Madison Square

Free on-site parking

Convenient access to on-site 24-7 fitness and wellness facilities

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Lead validation staff in developing, coordinating, and maintaining full SDLC validation deliverables for Medpace regulated software applications, including Validation & Test Plans, User Requirements & Functional Specifications, Functional & User Acceptance Testing, Traceability Matrices, and Validation Summary Reports;

Coordinate and assign systems and projects to validation staff according to priorities, timelines and availability;

Maintain oversight of validation staff in managing change control of Medpace software applications;

Ensure compliance of Medpace computer systems with GxP and SOx regulatory requirements;

Ensure compliance of system validation Standard Operating Procedures (SOPs) with regulatory requirements;

Ensure consistency of systems validation SOPs with best practices of industry;

Lead validation team in implementing tools and procedures to facilitate validation and documentation activities; and

Participate in Sponsor audits;

Bachelor's Degree;

7+ years of experience in SDLC, testing, and validation, preferably in an Agile environment and/or regulated industry;

Advanced knowledge of software development life cycle;

Knowledge and understanding of the application of Risk Management concepts;

Excellent analytical, written, and oral communication skills;

Previous supervisory experience is preferred; and

Experience in the regulated healthcare industry, with working knowledge of Good Clinical Practice and 21 CFR Part 11, is a plus!