About this role
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Job Description
Objectives
In this internship position, the intern will be a member of the Quality Assurance Support (QAS) team in providing quality oversight to the manufacturing team to ensure GMP compliance at Takeda Singapore.
Responsibilities
Quality Oversight
- Member of the QAS 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.
QA Support Operations
- Ensure timely release of raw materials for the site to support production
- Management of raw material reference samples.
- 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 QA Support documents.
Responsibilities
Quality Oversight
- Member of the QAS 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.
QA Support Operations
- Ensure timely release of raw materials for the site to support production
- Management of raw material reference samples.
- 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 QA Support 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 behaviour in accordance with Takeda’s Code of Conduct.
Any other duties as assigned by supervisor.
Education and Experience Requirements
- Background in Chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences, or equivalent
- Keen interest to work in a biopharmaceutical industry
Key Skills and Competencies
- 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 - WoodlandsWorker Type
EmployeeWorker Sub-Type
Paid Intern (Fixed Term) (Trainee)Time Type
Full timeOther facts
About Takeda
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
What you'll do
- The intern will provide quality oversight to the manufacturing team to ensure GMP compliance and support various quality systems. Responsibilities include timely release of raw materials, managing reference samples, and assisting with the development of standard operating procedures.
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