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6505 - Validation Engineer / CQV Engineer - Change Control & Deviations

Verista, Inc.
Location
Indianapolis, IN
Posted
24 days ago
Department
CQV Laboratory
What they actually want (must-haves)
  • Bachelor’s degree in Chemistry, Engineering, Life Sciences, or related field
  • 1-3 years of experience in CQV, Validation, or Quality Engineering in a regulated industry
  • Strong experience with change control systems
  • Experience in cGMP and GDP environments
  • Strong technical writing and documentation skills
  • Excellent communication and cross-functional collaboration abilities
Nice to have
  • Familiarity with analytical testing and Chemistry
  • Experience supporting validation lifecycle activities (IQ/OQ/PQ)
What the job really is

The CQV Engineer will support change control and deviation management activities in a regulated cGMP environment, ensuring compliance and quality systems are maintained. Responsibilities include authoring and managing change controls, performing impact assessments, collaborating with cross-functional teams, and participating in audits. The role requires strong technical writing skills and effective communication to facilitate timely change implementation.

Benefits
  • High growth potential and fast-paced organization with a people-focused culture
  • Competitive pay plus performance-based incentive programs
  • Company-paid Life, Short-Term, and Long-Term Disability Insurance
  • Medical, Dental & Vision insurances
  • FSA, DCARE, Commuter Benefits
  • Supplemental Life, Hospital, Critical Illness and Legal Insurance
Things to weigh
  • Onsite job requirement in Indianapolis, IN
  • Entry-level candidates encouraged to apply
  • Salary range provided but actual salary may vary based on multiple factors
Job score3.4/5
Benefits5/5
Freshness4/5
Career value4/5
Role clarity4/5
Pay transparency0/5

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