Laboratory Informatics & Validation Specialist

Verista, Inc.

Indianapolis (IN)

On-site

USD 74,000 - 104,000

Full time

14 days+
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Benefits offered by this job

Competitive pay
401(k) Retirement Plan
Paid Time Off

Job summary

Verista, Inc. is seeking a Validation Engineer to support laboratory and quality systems, ensuring compliant operation of instruments and software across the lifecycle.

You will coordinate software changes, document validation activities, and assist in deploying new equipment and systems within a regulated environment. Strong communication and problem-solving skills are essential for success in a fast-paced team.

Qualifications

  • Bachelor’s degree or higher in IT, engineering, life sciences, or related field.
  • 3+ years of experience supporting regulated computerized systems.
  • Experience in GxP-regulated pharmaceutical/biotech/medical device environments.
  • Hands-on with LIMS, Veeva, chromatography data systems, or related platforms.
  • Knowledge of validation, change control, and controlled documentation practices.

Responsibilities

  • Support daily operation of laboratories and quality systems, incl. instrument workstations and connectivity.
  • Coordinate software installs, upgrades, patches, and changes with users and support teams.
  • Maintain accurate technical documentation and lifecycle planning for hardware and software.
  • Assist deployment of new lab instruments and computerized systems, incl. workstation builds and migrations.
  • Coordinate vendor activities and document dependencies, risks, and issues for escalation.
  • Support computer system validation and software assurance activities across the lifecycle.
  • Execute qualification and testing activities with traceable evidence and deviations processing.
  • Collaborate with IT and cybersecurity on endpoint management, backups, and recovery.

Skills

GxP regulated environments
Troubleshooting & root cause
Documentation practices
Independent work

Education

Bachelor’s Degree in Information Technology, Engineering, Life Sciences, or related field

Tools

LIMS
Veeva
Chromatography data systems
Instrument software

Job description

Verista, Inc. is seeking a Validation Engineer to support laboratory and quality systems, ensuring compliant operation of instruments and software across the lifecycle.

You will coordinate software changes, document validation activities, and assist in deploying new equipment and systems within a regulated environment. Strong communication and problem-solving skills are essential for success in a fast-paced team.

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