Validation Engineer II

PacivIndianapolis, IN
69d

About The Position

PACIV is a global leader in industrial automation and process control solutions, serving clients in the life sciences, pharmaceutical, medical device, food & beverage, and utilities sectors, specializing in delivering compliant, high-performance automation systems tailored to regulated environments. We are seeking a detail-oriented and proactive Validation Engineer II for our Indianapolis, IN office to support compliance and efficiency in a regulated environment. This role is responsible for executing and managing periodic reviews of computer systems, and driving resulting action items to completion. The ideal candidate will collaborate cross-functionally to create, revise, and control technical documents, while also supporting system updates and process improvements.

Requirements

  • Bachelor's degree in a relevant field (e.g., Life Sciences, Engineering, Technical Writing, or Information Systems)
  • Minimum 8 years proven experience in validation documentation within regulated environments (e.g., pharmaceutical, biotech, or life sciences).
  • Strong understanding of Good Documentation Practices (GDP) and GMP compliance.
  • Experience with TrackWise or similar quality management systems.
  • Ability to collaborate with Subject Matter Experts to develop and revise technical documentation.
  • Excellent attention to detail and organizational skills.
  • Strong communication and stakeholder engagement abilities.

Responsibilities

  • Execute Periodic Reviews of all departmental computerized systems supporting Clinical Trials (i.e. Parts Washers, Autoclaves, Filtration Systems, etc.)
  • Create, track, and drive to completion action items for any deficiencies resulting from Periodic Reviews.
  • Update Computer System Validation (CSV) documentation which may include design documents, local policies and procedures, tools, forms, and assessments.
  • Support the development of reporting tools and methods to enhance visibility into periodic review progress and project metrics.
  • Review validation documentation and ensure accuracy and compliance with local department and industry standards.
  • Collaborate with cross-functional teams to ensure outputs of periodic reviews and any other CSV-related project deliverables meet local and regulatory requirements.

Benefits

  • Generous Paid Time Off - Vacation, sick leave, and company-recognized holidays.
  • Healthcare Coverage - PACIV covers 90% of your healthcare premium.
  • Health Savings Account (HSA) - Bi-monthly company contributions to cover out-of-pocket medical expenses.
  • 401(k) Retirement Plan - Company match up to 4% & full vestiture on enrollment date.

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What This Job Offers

Job Type

Full-time

Career Level

Mid Level

Industry

Computer and Electronic Product Manufacturing

Education Level

Bachelor's degree

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