MS&T Intern

MSD Malaysia; Swords; Hybrid; EUR 12,000 - 18,000; Part time

Job summary

MSD Malaysia is seeking a capable MS&T Intern to provide technical support across Manufacturing Sciences & Technology and Quality Control. The role emphasizes learning, collaboration with cross-functional teams, and contributing to process improvements in a regulated environment.

The internship offers exposure to regulatory compliance, documentation and Lean Six Sigma methodologies, with a hybrid work arrangement and a focus on developing practical skills in a global healthcare setting.

Qualifications

• Enrolled in or currently pursuing Bachelor’s degree in Biological Sciences, Chemical Engineering, Biological Engineering or Chemistry.
• Strong analytical problem solving and data analytics.
• Familiarity with cGMP and GMP regulations.
• Experience with data entry and documentation management.

Responsibilities

• Provide technical support to MS&T functions including training and assessments.
• Support MS&T activities aligned with business needs.
• Assist in investigations and CAPAs with root cause analysis.
• Participate in audits and regulatory inspections.
• Support lean six sigma initiatives to improve operations.

Skills

Analytical Problem Solving

Data Analytics

Technical Writing

Process Improvements

Lean Six Sigma

Manufacturing

Documentation

Education

Bachelor’s degree in Biological Sciences/Chemical Engineering/Biological Engineering/Chemistry

Job description

Job Description Position Overview

The Intern MS&T provides a range of technical support to the site in particular Manufacturing Sciences and Technology (MS&T). This is a learning role, but they can take a lead in utilising the latest innovations in technology and automation to create a workplace of the future.

Essential Functions and Responsibilities

• Provides technical support to Manufacturing and/or Quality Control including training, process and product impact assessments.
• Support activities in the MS&T department based on business requirements.
• Supporting multidisciplinary teams (manufacturing science and technology, quality, analytics, regulatory) for process improvement and troubleshooting with end-to-end product focus.
• Ensure compliance 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.
• Author/Review/Approve/Execute documentation in line with the standard process.
• Assist in and facilitate investigations, ensuring effective Root Cause Analysis and CAPAs.
• Participate in audits and inspections.
• Support continuous improvement through Lean Six Sigma methodologies.
• Support various site initiatives to improve compliance status and overall operational efficiency of the site.

Qualification and Skills Requirements

General competencies

• A self-starter and results-focused, the successful candidate will have strong contemporary knowledge, and the ability to work independently and on multidisciplinary teams.

Technical

• Oral and written communication skills, with the ability to effectively articulate understanding of process science, in order to drive decision making, in a multi-disciplinary team environment.
• Technical writing skills.

Education/Experience

• In the process of obtaining a Bachelor’s degree (or higher) in Biological Sciences/Chemical Engineering/Biological Engineering/Chemistry.

Required Skills

• Analytical Problem Solving
• Analytical Problem Solving
• Biological Engineering
• Biological Sciences
• cGMP Regulations
• Chemical Engineering
• Chemical Technology
• Clinical Research
• Data Analytics
• Database Management
• Data Entry
• Data Visualization
• Document Management
• Good Manufacturing Practices (GMP)
• Health Economics
• Lean Six Sigma (LSS)
• Manufacturing
• Office Applications
• Operational Efficiency
• Process Improvements
• Project Management
• Reporting and Analysis
• Six Sigma
• Technical Support
• Technical Training

Employee Details

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

Job Posting End Date

Job Posting End Date: 09/16/2026

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.