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Validation and Quality Assurance Consultant - Hamlyn Williams
We are currently partnered with a leading global pharmaceutical organisation to support the search for an experienced C&Q Engineer to join their team on a high-impact capital project at a key manufacturing site in Dublin.
This is a full-time, on-site contract opportunity. The successful candidate will play a key role in the commissioning and qualification of DeltaV systems, with a strong focus on troubleshooting I/O issues and ensuring compliance in a regulated GMP environment.
Key Responsibilities
* Execute commissioning and qualification protocols for DeltaV control systems
* Troubleshoot I/O and automation-related issues to support system readiness
* Perform GMP-compliant documentation and maintain accurate test records
* Collaborate with cross-functional teams including automation, QA, and operations
* Participate in site walkdowns, punch list resolution, and startup support activities
Essential Skills and Experience
* Strong track record resolving I/O and system-level issues during commissioning
* Minimum 3 years of experience in C&Q roles within GMP environments
* Experience working directly for end-user pharmaceutical clients
* Knowledge of cGMP, safety protocols, and qualification best practices
This is an excellent opportunity for a capable and hands-on C&Q professional to support a critical manufacturing project at one of Ireland’s most prominent pharma sites.
To apply or learn more, please submit your CV or reach out directly for a confidential discussion.
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Contract
Job function
* Industries
Pharmaceutical Manufacturing and Biotechnology Research
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