Digital Manufacturing Operations (DMO) Intern - Ballydine

MSD Malaysia; Ireland; On-site; EUR 18,000 - 34,000; Part time

Job summary

Merck & Co., Inc. in Ireland invites an Engineering/Automation intern to join our onboarding program. You will help develop process control applications and support automation components across operating areas.

Responsibilities include daily support, compliance with GMP, and collaboration with cross-functional teams. ENrolled in an automation/engineering/IT program with strong analytical skills is preferred.

Qualifications

• Currently enrolled in an automation/engineering/computer or other technical degree.
• PQ20 required skills are listed in the role description.
• Knowledge of data analytics, dashboards and reporting is advantageous.

Responsibilities

• Develop process control applications on automation platforms.
• Provide day-to-day support to operating areas for automation components.
• Ensure adherence to GMP and regulatory requirements.
• Manage user access reviews, backups and equipment maintenance.
• Collaborate with teams via daily Tier calls to address issues.
• Develop and support analytical dashboards for business needs.

Skills

Analytical Problem Solving

Automation Engineering

Business Processes

Data Analytics

Data Visualization

Document Management

Global Compliance

GMP

Industrial Automation

Project Management

Teamwork

Interpersonal Communication

Office Applications

Process Improvements

Reporting and Analysis

Regulatory Requirements

Education

3rd level Automation/Engineering/Computer discipline

Tools

CS Development Lifecycle

Automation Systems

Microsoft Office

Job description

Responsibilities

• Development of Process Control Applications on various automation platforms
• Provide day to day support to Operating Areas for Automation components of the process and collaborate with integrated process teams across the site.
• Ensure adherence with standards, following business processes in the execution and support of Automation systems
• Manage daily tasks like user access reviews, backup and restore tasks, install\troubleshoot\decommission equipment
• Participate in daily Tier calls, taking responsibility to collaborate with customers to address daily operational issues.
• Comply with 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.
• Work collaboratively to drive a safe and compliant culture
• Development and support of analytical dashboards to address business needs

Qualifications

Currently enrolled in an Automation, Engineering, Computer or other Technical discipline in 3rd level education. PQ20 Required Skills:

Required Skills

• Analytical Problem Solving
• Analytical Problem Solving
• Automation Engineering
• Business Processes
• Clinical Research
• Continued Process Verification
• Core Competencies
• Data AnalyticsDatabase Management
• Data Entry
• Data Visualization
• Document Management
• Global Compliance
• Good Manufacturing Practices (GMP)
• Health Economics
• Industrial Automation
• Interpersonal Communication
• Office Applications
• Process Improvements
• Project Management
• Project Management Support
• Regulatory Requirements
• Reporting and Analysis
• Teamwork
• Technical Support

{+ 2 more}

Core Competencies (Technical)

• Some knowledge of Computer System Development Lifecycle is preferred
• Some knowledge of automation systems is preferred
• Proficiency in Microsoft Office and job related computer applications required

Core Competencies (Business)

• Effective communication and interpersonal skills to interface effectively with all levels of colleagues in a team environment
• Self motivated
• Effective time management, multi-tasking and problem solving skills

Employment Information

• 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.

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.

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.