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Verista

GxP lifecycle consulting for life sciences

Validation Engineer / CQV Engineer

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeColumbus, OH, USA

About the Job

Requirements

  • A bachelor's degree or equivalent is required.
  • Proficiency using a PC and Microsoft Office tools is required.
  • Strong ability to communicate effectively with peers in clear, concise terms is required.
  • Ability to work as part of a team is required.
  • Strong problem-solving and critical-thinking skills are required.
  • Strong organizational and time-management skills are required.
  • Strong attention to detail is required.
  • Good Manufacturing Practice (GMP) and Good Documentation Practice training is required; this may be completed at onboarding.
  • Intermediate Microsoft Word skills are required, including authoring and editing large technical documents with styles, tables, tables of contents, and track changes.
  • Basic Microsoft Excel and PowerPoint skills are required.
  • Strong interpersonal skills and clear communication capabilities are required.
  • Availability to work second and/or third shift, five days per week onsite in Columbus, Ohio, is required.

Responsibilities

  • Author, edit, and execute technical commissioning, qualification, and validation documentation for standard equipment, systems, software, and processes as part of a team and as directed by the project leader.
  • Run test scripts and document results.
  • Adhere to the project schedule for all assigned activities.
  • Maintain clear, detailed qualification and validation records.
  • Read technical schematics to identify, locate, and test photo sensors, verify part numbers, and complete input/output testing on automated manufacturing equipment.

Desired Qualifications

  • Prior experience supporting validation, qualification, or testing activities for packaging equipment or packaging lines is preferred.
  • Experience working in or supporting pharmaceutical, medical device, combination product, or regulated packaging operations is a plus.

About the Company

Verista

GxP lifecycle consulting for life sciences

Verista provides business and technology consulting for life science companies, focusing on systems, compliance, validation and quality across the GxP lifecycle. Its services cover preclinical, clinical, commercialization, manufacturing and distribution to ensure safe, high-quality results. The company combines decades of industry knowledge with advanced engagement platforms and transformative technologies to help clients solve complex challenges with one partner across specialties. With a team of 500+ experts, Verista supports clients from strategy and validation to execution, delivering consistent, compliant outcomes that improve health and lives. The goal is to enable better health outcomes by ensuring products and processes are safe, compliant and efficient throughout the product development lifecycle.

Company size
201-500
Company stage
Not listed
Total funding
Not listed
Headquarters
Fishers, IN
Founded
2020

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