Verista, Inc.

Verista, Inc.

6244 - CIP (Clean-in-Place) CQV Engineer / Lead Validation Engineer

Apex, NC

Sponsorship not specified$108k-$168kDetected 62 days ago
PLCGMPLeadershipCommunication

About the role

  • Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.
  • Our talented and dedicated professionals are committed to making an impact every day.
  • The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice.

Responsibilities

  • Serve as the commissioning and qualification (C&Q) lead for CIP systems (responsibilities described below).
  • Develop and optimize CIP cleaning cycles to meet operational and quality standards.
  • Gain a thorough understanding of system design by reviewing engineering documentation, P&IDs, and design specifications.
  • Develop User Requirement Specifications (URS) and Quality Risk Assessment for Equipment and Automated Systems (QRAES).
  • Create Commissioning Test Plans that translate design intent into testable steps.
  • Develop Installation, Operational, and Qualification (IOQ) protocols.
  • Take custody of the system post-construction and maintain ownership through C&Q completion.
  • Perform Lockout/Tagout (LOTO) for system safety.
  • C&Q Lead Responsibilities
  • Engage with design engineers and SMEs to clarify system intent and operational requirements.

Requirements

  • Bachelor's degree in Engineering, Biotechnology, Life Sciences, or a related technical discipline
  • 10+ years of role-specific experience
  • Experience supporting CQV activities within GMP-regulated pharmaceutical or biotechnology environments
  • Hands-on experience with CIP systems and automated cleaning processes
  • Strong understanding of CQV lifecycle documentation (IQ/OQ/PQ protocols and reports)
  • Ability to work independently while coordinating with cross-functional project teams
  • Experience using digital validation platforms such as Kneat
  • Experience supporting FAT/SAT, commissioning, and equipment startup
  • Familiarity with automated process systems and PLC-based equipment
  • Experience in biologics or large-scale biopharmaceutical manufacturing environments

Compensation

  • For US geography, the salary range for this position is shown below.

Benefits

  • Company-paid Life, Short-Term, and Long-Term Disability Insurance.
  • Medical, Dental & Vision insurances
  • FSA, DCARE, Commuter Benefits
  • Health Savings Account
  • 401(k) Retirement Plan (Employer Matching benefit)
  • Paid Time Off (Rollover Option) and Holidays
  • Tuition Reimbursement
  • Paid Parental Leave and Bereavement

Company info

  • We empower and support our colleagues
  • We commit to client success at every turn
  • We have the courage to do the right thing
  • We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
  • We constantly acquire new skills and learn from our experiences to enhance our collective expertise
Apply directly at Verista, Inc. →Create a free account for alerts like thisView Verista, Inc. immigration profile

This listing is sourced directly from Verista, Inc.'s careers page and normalized into a canonical job model.