Validation Engineer

Position: Validation Engineer
Location: Blue Ash, OH
Duration: 12 Month Contract


Role Descriptions: •
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.


Must Have Technical/Functional 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, with the ability to drive decisions and deliver results without direct authority.


Roles & 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.

Generic Managerial Skills, If any
• Strong communication skills, with proficiency in reading, writing, and speaking English.
• Ability to multitask, understand customer requirements, and respond promptly and accurately.
• Capability to prioritize and manage multiple tasks in a fast - paced environment.
• Ability to understand and follow complex written procedures.
• Ability to work effectively in a team environment and contribute to team goals.
• Strong decision - making and problem - solving abilities with sound situational judgment.


Essential Skills: EIS : MDD Risk Management Desirable Skills:
Keyword:
Skills: EIS : New Product Development (NPD) Methodology and Management~EIS : MDD Risk Management Experience Required: 6-8

Diverse Lynx LLC is an Equal Employment Opportunity employer. All qualified applicants will receive due consideration for employment without any discrimination. All applicants will be evaluated solely on the basis of their ability, competence and their proven capability to perform the functions outlined in the corresponding role. We promote and support a diverse workforce across all levels in the company.