Engineering Services Intern

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Job Description

Engineering Services Intern

Scope of Internship:

The manufacturing site located in Woodlands, is one of the key biologics manufacturing sites in Takeda’s global network. The Site is dedicated to improving our ability to serve patients and through a commitment to excellence, focused on: Agile, Connected, Performance, Innovation and People.

In this role, the Engineering Services Intern will partner with various key stakeholders in the Takeda organization to perform sitewide responsibilities managed by the Engineering Services function, including qualification and validation activities.

If you are passionate and enthusiastic to learn the biopharmaceutical process at a holistic perspective, you will enjoy your learning journey with this fun and close-knit team.

The key responsibilities of the Engineering Services Intern include:

• Participates in commissioning and qualification activities related to Computer System Validation, Equipment Qualification, Temperature Controlled Systems Qualification (Freezers, Incubator etc), Clean Utilities Qualification, Cleaning Validation, SIP Validation and Shipping Validation in accordance with Takeda’s internal procedures and industry standards.

• Participates in the creation of equipment lifecycle documentations, e.g. FAT, SAT, IQ, OQ, PQ protocols and reports, risk assessments, technical specifications.

• Coordinates commissioning and qualification activities and the review of validation documentation.

• Participates in investigation revolving around discrepancies identified during qualification activities, working in collaboration with cross-functional teams.

• Coordinates and leads continuous improvement projects.

• Executes validation maintenance activities, e.g. executes periodic reviews, coordinates periodic monitoring activities and performs periodic requalification.

• Participates in validation meetings with cross functional teams in resolving validation issues.

• Responsibility to adhere to any applicable EHS requirements.

• Commitment to a fair and respectful relationship to others and behavior in accordance with Takeda’s Code of Conduct.

• Any other duties as assigned by supervisor.

Requirements:

• Keen interest to work in a biopharmaceutical industry

• Keen interest to explore commissioning, qualification and validation

• Knowledge and experience using Microsoft 365 applications

• Detail-oriented and proactive towards job responsibilities

• Good interpersonal, communication, presentation, and analytical skills

• Ability to interact with multiple stakeholders

• Good team player

• Independent with good initiatives and learning attitude 

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