Engineering IPT Internship - Brinny

MSD Malaysia; Cork; Hybrid; EUR 17,000 - 23,000; Full time

Job summary

Merck & Co., Inc. in Cork, Ireland invites an Engineering IPT Intern to support daily operations within a regulated manufacturing environment.

You will gain hands-on experience in audits, project support, data management, and continuous improvement over a 6–9 month period. The role requires pursuing a Bachelor’s Degree (Level 8) in Engineering and demonstrates strong analytical, organizational, and communication skills, with proficiency in Excel.

Qualifications

• Pursuing a Bachelor’s Degree (Level 8) in Engineering (Mechanical, Electrical, Chemical) or related discipline.
• Strong organizational and analytical skills; good communication and collaboration with Quality, EHS, and Manufacturing.
• Proficiency in Microsoft Office; proactive problem-solving and interest in pharma/biotech industry.

Responsibilities

• Engineering Audits & Inspections: conduct site walkthroughs to identify maintenance needs, safety hazards, and compliance issues.
• Project Support: assist with equipment upgrades and vendor management.
• EHS & Compliance: ensure GMP standards and safety protocols are followed.
• Data Management: prepare and update engineering metrics, KPI dashboards, and technical documentation.
• Continuous Improvement: participate in projects to improve equipment efficiency and reduce downtime.

Skills

Analytical problem solving

Cross-functional collaboration

Data analytics

Process improvements

Project management

GMP compliance

Teamwork

Education

Bachelor’s Degree (Level 8) in Engineering

Tools

Microsoft Office (Excel, Word, PowerPoint)

Job description

## Engineering IPT Internship - BrinnyApply: Not Applicable: IRL - Cork - Brinny: Full time: Posted Today: End Date: September 16, 2026 (2 days left to apply): R411788Job DescriptionThis 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 HERECurrent 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.**