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Validation Engineer / CQV Engineer

Verista Inc.Indianapolis, IN
On-site Full-time $60K/yr - $102.6K/yr

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Experience Level

Entry Level

Qualifications

Required Qualifications:Bachelor’s Degree or equivalent experience. Proficient in Microsoft Office Suite and general PC usage. Outgoing personality with exceptional communication skills, capable of articulating ideas clearly and concisely. Demonstrated ability to function effectively within a team environment. Strong analytical and problem-solving capabilities. Excellent organizational and time management skills. Meticulous attention to detail. Training in Good Manufacturing Practices (GMP) and Good Documentation Practices (may be completed during onboarding).

About the job

Job Overview

Verista, a leader in providing innovative solutions for the life sciences industry, collaborates with renowned brands to address critical business challenges. Our mission is to foster growth and innovation within the scientific community and assist researchers and organizations in overcoming significant healthcare obstacles. We pride ourselves on delivering services that empower informed decision-making, backed by our substantial investment in our workforce and capabilities.

Our success is fueled by a team of world-class professionals who excel in collaborative environments, sharing our vision to enhance the lives of clients in the life sciences sector. Our dedicated experts are resolute in their commitment to making a daily impact.

Company Culture and Values:

  • We empower and support our colleagues.
  • We are dedicated to client success at every opportunity.
  • We demonstrate the courage to do what is right.
  • We cultivate an inclusive environment where all colleagues feel respected, engaged, and challenged.
  • We continuously seek to expand our skills and learn from our experiences to elevate our collective expertise.

Key Responsibilities of Validation/CQV Engineer:

  • Develop, revise, and execute technical documentation related to commissioning, qualification, and validation for standard equipment, systems, software, and processes under the guidance of the project leader.
  • Execute test scripts and accurately document results.
  • Ensure compliance with project timelines for all assigned tasks.
  • Maintain comprehensive and detailed records pertaining to qualification and validation processes.
  • Interpret technical schematics to identify and test photo sensors, confirm part numbers, and perform input/output testing on automated manufacturing equipment.

About Verista Inc.

Verista Inc. prides itself on its team of 500 experts committed to driving innovation in the life sciences sector. By partnering with major brands, we enable growth and tackle some of the most pressing healthcare challenges. Our investment in our people and capabilities ensures that we deliver exceptional solutions and services.

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