Pharma Validation Intern: On‑Site QA & Process Improvement

MSD Malaysia; Carlow; On-site; EUR 13,000 - 18,000; Part time

Job summary

MSD Malaysia is offering an on-site internship in Carlow, Ireland, focusing on pharma validation and cycle development. You will contribute to qualification, documentation, and continuous improvement while collaborating with production and quality teams to ensure cGMP compliance.

The role targets students pursuing science or engineering, with emphasis on data analytics and problem solving in a global healthcare environment, ending as a fixed-term program.

Qualifications

• Pursuing a Science/Engineering qualification in a related discipline.
• Strong analytical and problem-solving abilities.
• Interest in pharmaceutical validation and compliance.

Responsibilities

• Author/Review/Execute qualification/validation documentation and cycle development studies.
• Author/Review/Execute change controls and investigate quality issues.
• Participate in troubleshooting during study execution and support continuous improvement.
• Engage with Production, Maintenance and Quality during Cycle Development activities.
• Plan and execute validation activities and support root cause analysis.

Skills

Analytical Problem Solving

cGMP Regulations

Data Analytics

Documentation Management

Quality Assurance

Regulatory Audits

Process Improvements

Project Management

Data Visualization

Team Collaboration

Education

Science/Engineering qualification in progress

Tools

MS Excel

Database Management

Office Applications

Job description

MSD Malaysia is offering an on-site internship in Carlow, Ireland, focusing on pharma validation and cycle development. You will contribute to qualification, documentation, and continuous improvement while collaborating with production and quality teams to ensure cGMP compliance.

The role targets students pursuing science or engineering, with emphasis on data analytics and problem solving in a global healthcare environment, ending as a fixed-term program.