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Senior Consultant at Morgan McKinley -Quality Assurance & Validation, Science Team
CQV Validation Engineer
An experienced CQV Validation Engineer is required for upcoming projects in the Dublin area. The role will involve supporting commissioning and qualification activities for process equipment, both new and repurposed with a strong focus on protocol development, documentation, and compliance.
Key Focus Areas:
* Development and execution of IOQ protocols and supporting documentation (FAT, SAT, IRA, traceability matrix, CSV-compliant files).
* Revalidation of existing process systems in line with current GMP requirements.
* Hands-on support for equipment installation, commissioning, and qualification lifecycle activities.
* Involvement with powder and liquid processes: blending, compression, granulation, fluid bed drying, automated filling, and packaging lines.
Ideal Profile:
* Proven background delivering end-to-end validation documentation in a regulated pharma environment.
* Good working knowledge of pharma manufacturing processes and equipment.
* Able to work independently with minimal supervision while meeting tight deadlines.
For further details or a confidential discussion, please get in touch or forward a brief profile.
Seniority level
* Seniority level
Associate
Employment type
* Employment type
Full-time
Job function
* Job function
Quality Assurance
* Industries
Pharmaceutical Manufacturing
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