INTERNSHIP DETAILS

Engineering IPT Internship - Brinny

CompanyMSD
LocationCork
Work ModeOn Site
PostedSeptember 13, 2026
Internship Information
Core Responsibilities
The intern will support daily engineering operations, maintenance needs, and continuous improvement projects within a regulated pharmaceutical manufacturing environment. Responsibilities include conducting site audits, managing equipment upgrades, and maintaining technical documentation in compliance with GMP standards.
Internship Type
full time
Company Size
39714
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
At MSD, known as Merck & Co., Inc., Rahway, NJ, USA in the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.msd.com and connect with us on Facebook, Instagram, Twitter, and YouTube.
About the Role

Job Description

This Engineering IPT Intern role in Cork, Ireland, supports a multinational pharmaceutical site's daily operations. You will help manage and gain hands-on experience in daily engineering activities and continuous improvement projects in a regulated manufacturing environment.

Role Overview

  • Location: Cork, Ireland
  • Duration: 6 - 9 Months
  • Department: Vaccines IPT
  • Reporting to: Engineering Manager

Key Responsibilities

  • Engineering Audits & Inspections: Conduct routine site walk-throughs to identify maintenance needs, safety hazards, and compliance issues across laboratories and manufacturing suites.
  • Project Support: Assist the engineering & operations teams with equipment upgrades and vendor management.
  • EHS & Compliance: Ensure all operations adhere strictly to Good Manufacturing Practice (GMP) standards, environmental sustainability goals, and safety protocols.
  • Data Management: Prepare and update engineering metrics, KPI dashboards, and technical documentation.
  • Continuous Improvement: Participate in projects to improve equipment efficiency and reduce operational downtime.

Requirements

  • Currently pursuing a Bachelor’s Degree (Level 8) in Engineering (Mechanical, Electrical, or Chemical), or a related discipline.
  • Strong organizational and analytical skills.
  • Excellent communication skills and the ability to collaborate with cross-functional teams (Quality, EHS, Manufacturing).
  • High proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).
  • A proactive approach to problem-solving and a keen interest in the pharmaceutical/biotech industry.

What You Will Learn

  • Direct, hands-on insight into how a highly regulated pharmaceutical manufacturing facility operates.
  • Experience working with global teams and industry-standard maintenance software.
  • Mentorship from seasoned engineering and manufacturing professionals.

PQ20

Required Skills:

Analytical Problem Solving, Analytical Problem Solving, Biopharmaceutical Industry, Clinical Research, Continuous Process Improvement, Cross-Functional Collaboration, Cross-Team Collaboration, Data Analytics, Database Management, Data Entry, Data Visualization, Document Management, Global Team Collaboration, GMP Compliance, Good Manufacturing Practices (GMP), Health Economics, Microsoft Office, Office Applications, Pharmaceutical Manufacturing, Process Improvements, Project Management, Reporting and Analysis, Safety Protocols, Teamwork, Technical Support {+ 1 more}

Preferred Skills:

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:

Not Applicable

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

N/A

Job Posting End Date:

09/16/2026

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Key Skills
EngineeringPharmaceutical ManufacturingGMP ComplianceProject ManagementData AnalyticsAnalytical Problem SolvingContinuous Process ImprovementCross-Functional CollaborationTechnical SupportDocument ManagementSafety ProtocolsMicrosoft OfficeEquipment MaintenanceVendor ManagementBiopharmaceutical IndustryReporting and Analysis
Categories
EngineeringManufacturingHealthcareScience & ResearchData & Analytics