Senior Validation Engineer
Contract Details:
* 12-month freelance contract
* Onsite in Dublin
* 40 hours/week, competitive hourly rate
Role Overview:
As a Validation Engineer, you will play a key role in ensuring that all equipment, systems, and processes meet regulatory and quality standards. You will work within a dynamic team environment, supporting the commissioning, qualification, and validation (CQV) of critical Equipment and Systems, driving compliance across all stages of the production lifecycle.
Key Responsibilities:
* Develop, execute, and maintain validation protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
* Analyze and interpret validation data, preparing detailed reports and recommendations.
* Ensure equipment and processes comply with Good Manufacturing Practices (GMP) and regulatory requirements (FDA, EMA).
* Participate in the commissioning of new equipment and systems, ensuring they meet design and operational specifications.
* Collaborate with cross-functional teams, including Quality Assurance, Production, and Maintenance, to troubleshoot and resolve validation-related issues.
* Maintain accurate and compliant documentation throughout the validation lifecycle.
* Stay updated on industry trends, regulatory changes, and best practices in validation and qualification.
What We’re Looking For:
* Bachelor’s degree in engineering, science, or a related technical field.
* 3+ years of experience in a validation role within the pharmaceutical, biotech, or life sciences industry.
* Strong understanding of GMP regulations, validation principles, and industry standards.
* Proficient in developing and executing validation protocols and managing validation documentation.
#J-18808-Ljbffr