Biotechnology Internship at Takeda Singapore
If you are searching for a Biotechnology Internship that offers hands-on industry experience, the Takeda Career internship program provides an excellent Internship in Singapore for aspiring scientists. This Internship opportunity for Life Science graduates allows students and early-career researchers to gain valuable exposure to pharmaceutical quality operations, GMP compliance, and manufacturing oversight. Through this Biotechnology Internship, interns will collaborate with experienced professionals and gain practical knowledge of global pharmaceutical quality systems, making it an ideal starting point for a Takeda Career in the biopharmaceutical industry.
Company Overview
At Takeda, Quality has always been a priority for us, throughout our long history. Today, what we do in Global Quality touches every part of our diverse organization. It’s reflected in our end-to-end Quality Management System that encompasses R&D, Manufacturing & Distribution, Commercial, Vaccines, and our BioLife Plasma collection network. When you’re a part of our team, you’ll do meaningful work that makes an impact on the lives of patients. Learn more about us and explore the opportunities to build a remarkable career.
Internship Details:
-
Location: Singapore (Woodlands site)
-
Company: Takeda Pharmaceutical Company
-
Worker Type: Employee
-
Worker Sub-Type: Paid Intern (Fixed Term) – Trainee
-
Time Type: Full-time
-
Job ID: R0175447
Internship Description
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 with the manufacturing team in the implementation and adherence to the various quality systems and GMP requirements at the manufacturing suite
- Participate in meetings 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 the supervisor.
QO Operations
- Review executed manufacturing batch records (MBR)
- Take on ownership for the investigation relating to quality operations.
- Support the manufacturing team with any quality interpretation, queries, and issues.
- Support the manufacturing team with the 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 a strong partnership with all other departments to ensure open communication 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 the supervisor.
Requirements:
- Background in Biochemistry, Biotechnology, or equivalent
- Keen interest in working in the 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 at emotional handling.
- Good time management skills
