Lab Technician & Validation Engineer — QC Impact

Verista, Inc.

Indianapolis (IN)

Sur place

USD 69 000 - 95 000

Plein temps

Il y a 8 jours
Générateur de candidature

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Avantages offerts par ce poste

Life Insurance (Company-paid)
Health Savings Account
Paid Time Off & Holidays
Tuition Reimbursement

Résumé du poste

Verista, Inc. seeks a Lab Technician / Validation Engineer in Indianapolis, IN to support QC laboratory activities and device testing. You will help ensure compliance with cGMP, 21 CFR 820, ISO standards, and related quality systems while assisting in equipment qualification (IQ/OQ/PQ) and batch release processes.

Join our team of 500+ experts dedicated to solving life science challenges. The role emphasizes collaboration, meticulous documentation, and ongoing development of lab procedures,

Qualifications

  • 3–5 years of regulated industry experience with knowledge of quality systems and regulatory requirements.
  • Strong problem solving and analytical thinking skills.
  • Strong verbal and written English communication skills.
  • Self-motivated with good self-management.
  • Computer literacy in Outlook, Windows, and Microsoft applications.
  • Excellent teamwork and ability to multi-task.
  • Strong curiosity and ability to identify issues and drive resolution.
  • Solid critical thinking and problem-solving abilities.

Responsabilités

  • Provide quality control support for the QC laboratory.
  • Assist in equipment qualification testing (IQ, OQ, PQ).
  • Maintain laboratory notebooks and reference samples.
  • Support regulatory inspections and deviations oversight.

Connaissances

Problem solving
Analytical thinking
Communication skills (English)
Self-management
Teamwork
Multi-tasking
Curiosity
Critical thinking

Outils

Microsoft Office
Outlook
Windows

Description du poste

Verista, Inc. seeks a Lab Technician / Validation Engineer in Indianapolis, IN to support QC laboratory activities and device testing. You will help ensure compliance with cGMP, 21 CFR 820, ISO standards, and related quality systems while assisting in equipment qualification (IQ/OQ/PQ) and batch release processes.

Join our team of 500+ experts dedicated to solving life science challenges. The role emphasizes collaboration, meticulous documentation, and ongoing development of lab procedures,

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