🏗️ Build the Foundation of Biopharmaceutical Manufacturing Excellence
Primary Objective
In this role, the Engineering Services Intern will partner with key stakeholders across Takeda to perform sitewide commissioning, qualification, and validation (CQV) activities. You will gain hands-on experience ensuring that critical systems and equipment meet stringent regulatory and quality standards, supporting the reliable production of life-saving biopharmaceuticals.
đź“Ť Location:Â SGP - Singapore - Woodlands
👨‍🔬 Worker Type: Paid Intern (Fixed Term Trainee)
⏰ Time Type: Full time
đź“‹ RESPONSIBILITIES
⚙️ Commissioning, Qualification & Validation Execution
- Participate in commissioning and qualification activities across critical areas:
- Computer System Validation (CSV)
- Equipment Qualification
- Temperature Controlled Systems (Freezers, Incubators)
- Clean Utilities Qualification
- Cleaning Validation, SIP Validation, and Shipping Validation
- Assist in creating equipment lifecycle documentation: FAT, SAT, IQ, OQ, PQ protocols/reports, risk assessments, and technical specifications.
đź“‹ Documentation & Coordination
- Support the review and coordination of validation documentation.
- Participate in investigations of discrepancies identified during qualification, collaborating with cross-functional teams.
- Attend validation meetings to help resolve technical and compliance issues.
🔄 Continuous Improvement & Maintenance
- Assist in continuous improvement projects within Engineering Services.
- Execute validation maintenance activities: periodic reviews, requalification, and monitoring coordination.
- Ensure all activities comply with Takeda procedures, industry standards, and EHS requirements.
👤 EDUCATION AND EXPERIENCE REQUIREMENTS
- Educational background in Biotechnology, Biological Sciences, Pharmaceutical Sciences, or Engineering.
- Keen interest in the biopharmaceutical industry and commissioning, qualification, and validation (CQV).
- Proficiency in Microsoft 365 applications.
- No prior experience required—comprehensive training will be provided.
🌟 KEY SKILLS AND COMPETENCIES
- Detail-Oriented & Proactive:Â Meticulous approach with initiative in assigned responsibilities.
- Strong Communicator:Â Excellent interpersonal, presentation, and analytical skills.
- Collaborative Team Player:Â Ability to interact effectively with multiple stakeholders and cross-functional teams.
- Independent Learner:Â Self-motivated with a strong attitude for learning and growth.
- Adaptable & Organized:Â Ability to manage multiple tasks in a dynamic GMP environment.
đź’Ľ WHY JOIN THIS INTERNSHIP?
- Technical Hands-On Experience: Gain direct exposure to CQV lifecycle activities in a state-of-the-art biopharmaceutical facility.
- Cross-Functional Exposure: Collaborate with Engineering, Quality, Manufacturing, and Validation teams.
- Career Foundation: Build specialized skills for roles in Validation Engineering, Process Engineering, Quality Assurance, or Regulatory Compliance.
- Professional Mentorship:Â Learn from industry experts in a structured, supportive environment.
- Paid Opportunity:Â Competitive compensation while developing highly sought-after technical and regulatory skills.
🎯 IDEAL FOR STUDENTS IN:
- Biotechnology / Bioengineering
- Pharmaceutical Sciences / Chemical Engineering
- Mechanical / Electrical / Process Engineering
- Life Sciences with an interest in engineering applications
🚀 READY TO ENGINEER QUALITY INTO EVERY SYSTEM?
👉 APPLY NOW FOR THE ENGINEERING SERVICES INTERNSHIP IN SINGAPORE.
Takeda is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
