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Engineering Test Pilot Jobs in Ohio (NOW HIRING)

Position Overview Power your future with Qualus in our Field Engineering department as a Senior ... Support in writing procedures and/or test plans in support of maintenance and construction ...

Senior Relay Field Technician

Cincinnati, OH · On-site

$19 - $26/hr

Position Overview Power your future with Qualus in our Field Engineering department as a Senior ... Support in writing procedures and/or test plans in support of maintenance and construction ...

Showing results 41-60

Engineering Test Pilot information

What are some common challenges faced by engineering test pilots during flight testing, and how are they addressed?

Engineering Test Pilots often encounter challenges such as unexpected aircraft behavior, rapidly changing test parameters, and the need to communicate complex technical feedback to engineers. To address these challenges, they follow strict safety protocols, participate in extensive pre-flight briefings, and work closely with multidisciplinary teams to anticipate and mitigate risks. Continuous training and simulation exercises also help test pilots prepare for a range of scenarios, ensuring that data collected is accurate and safety is maintained throughout the testing process.

What is an engineering test pilot?

Engineering test pilots are specialized aviators responsible for flying prototype, experimental, or modified aircraft to evaluate their performance, handling, and safety. They work closely with aircraft engineers and designers to collect data, identify issues, and provide feedback that informs design improvements. Their role is critical in the development and certification of new or updated aircraft, ensuring they meet regulatory and safety standards. Engineering test pilots must have advanced flying skills, technical knowledge, and the ability to assess complex systems under various flight conditions.

What are the key skills and qualifications needed to thrive as an engineering test pilot?

To thrive as an Engineering Test Pilot, you need an advanced pilot license (often ATP or military equivalent), a strong engineering or aeronautical background, and extensive flight experience. Familiarity with flight test instrumentation, data analysis software, and certification processes such as FAA or EASA regulations is crucial. Exceptional problem-solving, communication, and risk management skills set top candidates apart in this high-stakes field. These abilities are essential for safely conducting test flights, accurately evaluating aircraft performance, and collaborating with multidisciplinary teams to advance aerospace innovation.

What is the difference between Engineering Test Pilot vs Flight Test Engineer?

AspectEngineering Test PilotFlight Test Engineer
CredentialsPilot certifications, engineering backgroundEngineering degree, flight testing experience
Work EnvironmentIn-flight testing, aircraft operationGround testing, data analysis
Industry UsageAerospace, defense, aircraft developmentAerospace, aircraft certification

Engineering Test Pilots primarily operate aircraft during flight tests, combining piloting skills with engineering knowledge. Flight Test Engineers focus on planning, data collection, and analysis during testing, often working on the ground. Both roles are essential in aerospace development but differ in responsibilities and daily tasks.

What are popular job titles related to Engineering Test Pilot jobs in Ohio? For Engineering Test Pilot jobs in Ohio, the most frequently searched job titles are:
Infographic showing various Engineering Test Pilot job openings in Ohio as of August 2026, with employment types broken down into 86% Full Time, and 14% Contract. Highlights an 93% In-person, and 7% Hybrid job distribution.

Senior Medical Device Quality Engineer

Prophecy Technologies

Blue Ash, OH • On-site

$81K - $110K/yr

Full-time

Posted 10 days ago


Job description

Role Overview:
This Senior Medical Device Quality Engineer role involves leading multiple high-priority lifecycle change projects from concept through implementation within the medical device or other regulated industries. The position requires strong expertise in design controls, risk management, quality management systems, and process validation to ensure regulatory compliance and product quality.
Key Responsibilities:
  • Lead multiple high-priority lifecycle change projects from concept through implementation.
  • Drive project plans, timelines, risk mitigation strategies, and implementation readiness.
  • Coordinate cross-functional teams across Engineering, Quality, Regulatory, Manufacturing, Supply Chain, Procurement, Operations, and external suppliers.
  • Serve as the technical interface with suppliers for component development, DFM reviews, tooling readiness, process capability, and component qualification.
  • Support design verification and validation activities, including test planning, execution, data review, and technical documentation.
  • Partner with manufacturing sites on process validation activities, including IQ/OQ/PQ, pilot builds, validation builds, and production launch readiness.
  • Apply strong knowledge of design controls, engineering change management, risk management, quality system requirements, and regulatory expectations.
  • Review engineering drawings, specifications, GD&T requirements, tolerance analyses, and component acceptance criteria.
  • Drive root cause analysis, technical problem solving, and timely closure of project issues.
  • Communicate project status, risks, decisions, and recommendations clearly to stakeholders and senior leadership.
  • Demonstrate strong ownership, urgency, accountability, and ability to influence without direct authority.

Required Skills:
  • Strong expertise in Medical Device Product Lifecycle Management (PLM), Design Controls, and Engineering Change Management (ECO/ECN/ECR).
  • Hands-on experience with Design Verification & Validation (V&V), test methods, protocol development, and technical documentation.
  • Deep understanding of Risk Management methodologies, including ISO 14971, DFMEA, PFMEA, and hazard analysis.
  • Knowledge of Quality Management Systems (QMS), ISO 13485, FDA 21 CFR Part 820/QMSR, and regulatory compliance requirements.
  • Experience in Supplier Quality Engineering, component qualification, supplier development, and Design for Manufacturability (DFM).
  • Proficiency in Process Validation activities including IQ/OQ/PQ, pilot builds, validation builds, and manufacturing transfer.
  • Ability to interpret engineering drawings, GD&T, tolerance stack-ups, specifications, and acceptance criteria.
  • Strong root cause analysis and problem-solving skills utilizing 8D, CAPA, 5 Why, Fishbone, and corrective action processes.
  • Excellent project management skills, including planning, scheduling, risk management, stakeholder management, and cross-functional coordination.
  • Effective leadership, communication, and influencing skills.
  • EIS : MDD Risk Management.

Qualifications:
  • 6-8 years of experience required.
  • 7+ years of engineering experience in medical device or other regulated industries.
  • Experience leading cross-functional technical projects.
  • Experience with component development, supplier qualification, design verification, and manufacturing validation.
  • Strong understanding of design controls, change management, risk management, process validation, and quality system compliance.

Preferred Skills:
  • EIS : New Product Development (NPD) Methodology and Management.