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Senior Validation Engineer

EnIn Systems
NY Full Time
POSTED ON 2/8/2025 CLOSED ON 5/8/2025

What are the responsibilities and job description for the Senior Validation Engineer position at EnIn Systems?

Job Description :

We are seeking a highly skilled Senior Validation Engineer to join our team in the MedTech / Medical Devices sector. The successful candidate will play a critical role in ensuring the quality and compliance of products, systems, and processes in accordance with regulatory requirements.

Key Responsibilities :

  • Lead validation activities for medical devices, software, or systems, ensuring compliance with FDA, ISO, and other regulatory standards (e.g., 21 CFR Part 820, ISO 13485).
  • Develop, review, and execute validation protocols (IQ, OQ, PQ), including writing validation plans, reports, and specifications.
  • Coordinate and lead cross-functional teams to complete validation tasks and support product lifecycle management.
  • Review and approve engineering changes and deviations, ensuring that validation is maintained throughout the product lifecycle.
  • Perform risk analysis and implement corrective actions to resolve issues in the validation process.
  • Conduct design reviews and ensure validation requirements are addressed early in the design phase.
  • Maintain and update documentation to ensure that all validation processes are well-documented and easily auditable.
  • Provide technical leadership and mentorship to junior validation engineers.
  • Collaborate with R&D, Quality Assurance, and Manufacturing teams to ensure effective validation execution.
  • Ensure that validation processes align with company quality systems, processes, and objectives.

Qualifications :

  • Bachelor's degree in Engineering, Life Sciences, or a related field.
  • Minimum of 7 years of experience in validation engineering, preferably in the medical device or regulated industry.
  • In-depth knowledge of FDA regulations, ISO standards, and other applicable industry guidelines (e.g., 21 CFR Part 820, ISO 13485).
  • Experience with risk management tools such as FMEA, HACCP, or similar methodologies.
  • Strong problem-solving skills and attention to detail.
  • Ability to work in a fast-paced environment and manage multiple projects simultaneously.
  • Excellent communication and interpersonal skills.
  • Familiarity with computer software validation (CSV) and automation validation is a plus.
  • Experience with 3D printing, digital health, or software as a medical device (SaMD) is a plus.
  • Preferred Qualifications :

  • Certification in Validation (e.g., ISPE, ASQ, or other related credentials).
  • Experience with Lean Six Sigma or other process improvement methodologies.
  • Familiarity with risk management and quality management systems in the medical device industry.
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