New Product Introduction, Technical Engineering Internship

MSD Malaysia; Carlow; On-site; EUR 20,000 - 26,000; Full time

Job summary

MSD Malaysia is seeking an Intern for the NPI/Tech Transfer Team to support New Product Introductions and Technical Transfers. You will assist with process development, equipment qualification, and data analyses in a fast-paced biopharma environment.

The role offers exposure to GMP, quality systems, and cross-functional collaboration within manufacturing and technical operations. Ideal candidates are pursuing a science or engineering degree and possess strong analytical and communication skills.

Qualifications

• Currently pursuing a Bachelor's degree or higher in science, engineering or a technical discipline.
• Knowledge of regulatory/code requirements to Irish, European, and International Standards is a plus.
• Excellent communication, presentation, and interpersonal skills to interface with colleagues and external customers.

Responsibilities

• Support New Product Introductions and Technical Transfers.
• Coordinate qualification and validation activities for equipment and processes.
• Contribute to data analyses and root cause investigations.
• Prepare and review qualification/validation documentation.
• Assist in continuous improvement and Lean Six Sigma initiatives.
• Collaborate with cross-functional teams and external vendors as needed.

Skills

Analytical thinking

Problem solving

Data analytics

Documentation management

GMP compliance

Education

Bachelor's degree or higher in Science/Engineering or other Technical discipline

Tools

Excel

Databases

Office applications

Job description

Job Description Intern - NPI/Tech Transfer Team We aspire to be the premier research-intensive biopharmaceutical company. Join our NPI/Tech Transfer team and be at the forefront of innovation, supporting New Product Introductions and Technical Transfers. This is an exciting opportunity to bring your energy, knowledge, and leadership to a dynamic team dedicated to advancing health solutions.

Responsibilities Supporting New Product Introductions/Technical Transfers Provide process, technical, and validation support operations including ongoing support of manufacturing processes and support for new product introduction Conduct analytical/engineering studies associated with the development of new components, products, processes systems, and facilities Coordinate, design, and execute equipment qualification and validation as required Serve as technical and/or validation support for manufacturing and new product introduction Design/Author/Review/Approve/Execute process development studies in support of new product introduction and ongoing manufacturing support Provide technical input into quality notifications by authoring/reviewing/approving investigations Execute equipment commissioning and qualification programs Execute equipment/qualification validation programs, including re-qualification and re-validation Design/Author/Review/Approve/Execute qualification/validation documentation and studies in line with the standard approval process Perform data analysis and make informed decisions/recommendations based on conclusions from data analysis Support continuous improvement through Lean Six Sigma methodologies Lead and actively participate in projects, system failure investigations, and investigation reports Execute/develop change controls Contribute to Kaizen events as appropriate Perform root cause analysis of system failures and implement corrective actions through the change management system Serve as technical engineering representative for internal technical group discussions and represent the site at global technical forums Participate and/or lead cross‑functional or single‑function teams, including liaising with vendors or above‑site groups Drive compliance with Global Policies, Procedures, and Guidelines, regulatory requirements, and execute current Good Manufacturing Practices (cGMP) in daily activities Ensure compliance through documentation completion, risk assessments, closing out corrective actions, participating in audits and inspections, and proactively highlighting any compliance issues Work collaboratively to drive a safe and compliant culture on site Perform other duties as assigned.

Qualifications Required Currently studying Bachelor’s Degree or higher in a Science, Engineering, or other Technical discipline Knowledge of regulatory/code requirements to Irish, European, and International Codes, Standards, and Practices Excellent communication, presentation, and interpersonal skills to interface effectively with all levels of colleagues and external customers in a team‑oriented manner Understanding of the specific responsibilities of all site departments as they relate to one’s own department and the business processes it supports.

PQ20 Required Skills: Analytical Problem Solving, Analytical Problem Solving, Biopharmaceutical Industry, Biopharmaceuticals, Change Management, Clinical Research, Corrective Action Management, Data Analytics, Database Management, Data Entry, Data Visualization, Document Management, Equipment Qualification, GMP Compliance, Good Manufacturing Practices (GMP), Health Economics, Lean Six Sigma (LSS), Manufacturing Support, Office Applications, Process Improvements, Production Support, Project Management, Regulatory Requirements, Reporting and Analysis, Six Sigma {+ 2 more}.

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.

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.