Assoc. I, Administrative Services

Validation Intern

Our company is looking for a Validation Intern to start your journey on a career path within the Pharmaceutical industry. Not only will you learn both technical and professional skills but work on projects that will help enhance and improve people's lives across the world.

You will be part of a diverse and inclusive, multi-skilled global team of highly motivated individuals. We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's most challenging healthcare needs.

So, what will you be responsible for?

• Author/Review/Execute qualification/validation documentation and cycle development studies in line with the standard approval process.
• Author/Review/Execute execution/development of change controls.
• Participate in the troubleshooting of technical issues encountered during study execution.
• Engagement with Production, Maintenance and Quality representatives in the assigned area of operations during execution of Cycle Development & Performance Qualification activities.
• Technical input into quality notification by authoring/reviewing investigations.
• Execute production floor based activities.
• Plan and execute validation activities as required.
• Support root cause analysis of system failures, substandard performance, using standard tools and methods, to resolve machine and system issues.
• Support continuous improvement through Lean Six Sigma methodologies.
• Serve as validation representative for cross functional projects.
• Drive compliance of Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good Manufacturing Practices (cGMP) in the performance of day-to-day activities and all applicable job functions, ensuring consideration of the impact on GMP and compliance and decisions made.
• Responsible for compliance via documentation completion, risk assessments, closing out corrective actions, participation in audits and inspections and proactively highlighting any issues around compliance.
• Supporting regulatory audits and submissions as required.
• Work collaboratively to drive a safe and compliant culture in Carlow.
• May be required to perform other duties as assigned.

This internship will be completed fully on site (Carlow).

The ideal person will have:

• Working towards a Science qualification or relevant discipline.

Intern/Co-op (Fixed Term)

No relocation

No VISA Sponsorship

No Travel Required

Hybrid Flexible Work Arrangements

Not Indicated Shift

No Valid Driving License Required

n/a Hazardous Material(s)

Required Skills: Analytical Problem Solving, Clinical Research, Communication, Data Analytics, Database Management, Data Entry, Data Visualization, Document Management, Global Compliance, Global Team Collaboration, GMP Compliance, Good Manufacturing Practices (GMP), Health Economics, Management Process, Manufacturing Compliance, Office Applications, Pharmaceutical Management, Process Improvements, Project Management, Regulatory Compliance Consulting, Regulatory Requirements, Reporting and Analysis, Risk Assessments, Six Sigma

Job Posting End Date: 09/17/2025