CQV Engineer
Contract: 12 Months (Potential for Extension)
Type: Full-time, On-site
Overview
We are seeking an experienced CQV Engineer to support a broad range of capital and site-based projects. This role will work across both the Projects and Validation departments, collaborating closely with existing CQV engineers and cross-functional teams. The successful candidate will bring a wide range of CQV expertise and the flexibility to adapt to diverse project scopes.
Responsibilities
* Deliver commissioning, qualification, and validation (CQV) activities across multiple projects simultaneously.
* Support upgrades and modifications to utilities, process equipment, filling/packaging lines, and laboratory facilities.
* Collaborate with both the Projects and Validation departments to ensure alignment of CQV deliverables.
* Interface with other CQV engineers, both broad-based and specialist, to ensure project goals are met.
* Prepare and execute CQV documentation in compliance with internal standards and regulatory requirements.
* Provide technical support during new product introduction, scale-up, and clinical supply projects.
* Participate in project meetings, providing CQV input and updates.
* Ensure timely completion of CQV tasks to meet project schedules.
Requirements
* Minimum 5 years' experience within the pharmaceutical industry.
* Proven background in commissioning, qualification, and validation across:
*
o Process equipment
*
o Utility systems
*
o Fill/pack systems
* Strong understanding of GMP and regulatory compliance standards.
* Ability to work across multiple teams and manage competing project priorities.
* Excellent communication and problem-solving skills.
* Ability to adapt quickly to different project scopes and requirements.
Additional Information
* Reporting line to the Projects or Validation Manager.
* Interviews will be conducted in one stage (with potential for a second round)
* Start date targeted for early in the new year.