INTERNSHIP DETAILS

QO Intern

CompanyTakeda
LocationSingapore
Work ModeOn Site
PostedMarch 24, 2026
Internship Information
Core Responsibilities
The intern will provide quality oversight to the manufacturing team, ensuring GMP compliance, and will act as a Quality Systems Representative by partnering with manufacturing on quality systems implementation. Responsibilities also include reviewing manufacturing batch records, leading quality investigations, and supporting SOP/MBR development.
Internship Type
full time
Company Size
37190
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
We strive to transform lives. While the science we advance is constantly evolving, our core purpose is enduring. For more than two centuries, our values have guided us to do what’s right for patients and for society. We know that changing lives requires us to do things differently. We start by listening to and addressing what really matters to patients, the people who love them, and those in the healthcare system who provide care. And that’s what inspires us all to be bold, push boundaries and set new standards that open up greater opportunities. Read our community guidelines: https://takeda.info/communityguidelines
About the Role

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use.  I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description

Objective:

In this internship position, the intern will be a member of the Quality Operations (QO) team in providing quality oversight to the manufacturing team to ensure GMP compliance at Takeda Singapore.

Responsibilities

 

Quality Systems Representative

  • Member of the QO team in ensuring quality oversight at the manufacturing suite
  • Partner the manufacturing team in the implementation and adherence to the various quality systems and GMP requirements at the manufacturing suite
  • Participate in meeting with the manufacturing for information learning/sharing and alignment of best practices
  • Support the compliance, regulatory, inspections and training activities as required and any other responsibilities as assigned by supervisor.

 

QO Operations

  • Review executed manufacturing batch records (MBR)
  • Take on ownership for investigation relating to quality operations.
  • Support the manufacturing team with any quality interpretation, queries and issues.
  • Support the manufacturing team with development and writing of process standard operating procedures and master batch records ensuring compliance with current good documentation practices and the applicable global procedures and regulatory requirements.

 

Other responsibilities (if assigned)

  • Perform timely archival of QO documents.

 

Leadership

  • Build strong partnership with all other departments to ensure open communications and acceptance
  • 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:

  • Background in Chemistry, Biochemistry, Biotechnology or equivalent
  • Keen interest to work in a biopharmaceutical industry
  • Knowledge and experience using Microsoft Office
  • Committed to the role assigned.
  • Positive mindset and motivated.
  • Able to understand constraints at times and be flexible.
  • Good Interpersonal, Verbal and Written Communication Skills required.
  • Ability to work and collaborate within the team.
  • Good in emotional handling.
  • Good time management skills 

Locations

SGP - Singapore - Woodlands

Worker Type

Employee

Worker Sub-Type

Paid Intern (Fixed Term) (Trainee)

Time Type

Full time
Key Skills
Quality OversightGMP ComplianceQuality SystemsRegulatory InspectionsBatch Record ReviewInvestigationSOP DevelopmentDocumentation PracticesArchivalCommunicationMicrosoft OfficeTime ManagementEmotional Handling
Categories
ManufacturingScience & ResearchHealthcareEngineering
QO Intern - InternshipsHQ