CQV Engineer

Boston, MA, US • Posted 16 days ago • Updated 1 hour ago
Contract W2
On-site
Fitment

Dice Job Match Score™

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Job Details

Skills

  • Problem Solving
  • Test Planning
  • Construction
  • Biotechnology
  • Biomedical Engineering
  • Quality Management
  • Self Motivation
  • Data Logging
  • Safety Principles
  • Engineering Validation Tests
  • Rapid Learning
  • Management of Facilities
  • Business Partnerships
  • Gene Therapy
  • Geographic Information Systems
  • Receptivity

Summary

Job Title : CQV
Location : Boston, MA

General position summary:
The Engineer is actively involved in Commissioning, Qualification, Validation, and Requalification activities for Cell and Gene Therapy facilities. The individual is responsible for executing qualification protocols facilities and collaborate with Global Engineering, Facilities Operations, GIS, QA and PMO throughout the life cycle of the project.

Key Responsibilities:
The responsibilities of this position may include, but are not limited to, the following:

  • Develops and executes qualification and validation test plans and protocols.
  • Ensures that all validation documents align with the current client SOPs, global standards and cGMP guidelines.
  • Coordinates with personnel onsite and other vendors to schedule and execute test plans.
  • If required, coordinates with the construction team and Vertex operations teams to schedule execution of validation activities, safely and effectively.
  • Effectively works with cross functional departmental stakeholders, PMO, GIS, EH&S, Global Security, design teams, EHS and QA.
  • Completes Vertex assigned training and ensures that they are 100% compliant 100% of the time.
  • Supports right-the-first time culture for all documents distributed across the organization.
  • Ensures the Global Engineering reputation and partnership is flourished with the cross-functional teams.

Minimum qualifications:

  • Receptive to change Adapts (quickly) to changing circumstances.
  • Minimum Bachelor's degree in an Engineering (Chemical, Biomedical, Industrial, Biotechnology) or related discipline with 2-4 years of CQV experience or equivalent professional experience.
  • Self-motivated and must be able to work independently with minimal supervision and direction.
  • Experience in developing and executing protocols in GMP industry.
  • Experience using Kaye Validator and Data loggers.
  • Understanding and application of technical principles, theories, and concepts in the field, GMP, ISO, GAMP, ANSI.
  • Ability to learn and demonstrate technical problem solving and troubleshooting skills
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 91090330
  • Position Id: 2026-3560
  • Posted 16 days ago
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