Assoc. I, Administrative Services

Our company as Validation Intern to start your journey on a career path within the Pharmaceutical industry. Not only will you learn both technical and professional but work on projects that will contribute towards enhancing and enhancing 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.

• 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.

• Working towards a Science qualification or relevant discipline

PQ20

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status: Intern/Co-op (Fixed Term)

Relocation: No relocation

VISA Sponsorship: No

Travel Requirements: No Travel Required

Flexible Work Arrangements: Hybrid

Shift: Not Indicated

Valid Driving License: No

Hazardous Material(s): n/a

Required Skills: Analytical Problem Solving, 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

Preferred Skills:

Job Posting End Date: 09/17/2025

Requisition ID: R363344