Senior Validation Engineer

The Senior Validation Engineer coordinates all validation activities by constant communication with affected departments and personnel; oversees and reviews validation area processes and procedures. Prepares all protocols and reports for validation work. Being a Senior Validation Engineer typically reports to a manager or head of a unit/department. May require a bachelor’s degree. Being a Senior Validation Engineer contributes to moderately complex aspects of a project. Work is generally independent and collaborative in nature. Working as a Senior Validation Engineer typically requires 4 to 7 years of related experience.

Senior Validation Engineer Job Description Template

Our company is looking for a Senior Validation Engineer to join our team.

Responsibilities:

  • Create test plans, test scripts and working closely with the developers to understand the features and implementation;
  • Author detailed software quality requirements to meet Intel quality standards;
  • Train the team on quality engineering practices;
  • Help to support a team of junior SQA Engineers to mentor and guide them in the quality assurance work performed across multiple teams and projects;
  • Drive effective software practices to ensure project work products comply with applicable standards, requirements;
  • Work closely with upper management to provide a status report and health of products from a quality standpoint;
  • Provide input into program deliverables/milestones regarding quality resources, schedule, goals, etc.

Requirements:

  • Excellent written communication skills in English;
  • Excellent written communication skills are required;
  • Bachelor degree from accredited institution in Science or Engineering;
  • Knowledge of current validation principles and industry practices, including FDA regulations, cGMPs, and validation guidance documents is required;
  • Ability to structure validation protocols in conformance with a planned validation approach is required;
  • 5+ years of experience in Pharma or regulated industry;
  • Strong background and experience in Validation and GMP regulations;
  • No C2C;
  • Knowledge of basic engineering principles and practices, equipment automation controls, etc. is required;
  • No Third Party Resumes;
  • Familiarity with quality engineering practices in manufacturing operations is required;
  • No Sponsorship.