About this role
The intern will provide quality oversight to the manufacturing team to ensure GMP compliance and support various quality systems and regulatory activities. Responsibilities include reviewing manufacturing batch records, supporting investigations, and developing standard operating procedures.
Candidates should have a background in Chemistry, Biochemistry, Biotechnology, or equivalent, and a keen interest in the biopharmaceutical industry. Good interpersonal, verbal, and written communication skills are required, along with the ability to work collaboratively within a team.
What they're looking for
ChemistryBiochemistryBiotechnologyMicrosoft OfficeInterpersonal SkillsVerbal CommunicationWritten CommunicationTime Management
Frequently asked questions
What does a QO Intern at Takeda do?
The intern will provide quality oversight to the manufacturing team to ensure GMP compliance and support various quality systems and regulatory activities. Responsibilities include reviewing manufacturing batch records, supporting investigations, and developing standard operating procedures. Candida…
What skills does this QO Intern role need?
Key skills for this role include Chemistry, Biochemistry, Biotechnology, Microsoft Office, Interpersonal Skills, Verbal Communication.
How much does a QO Intern at Takeda pay?
The employer did not list a salary for this role. Most similar Singapore roles publish their band on the job page.
Is this QO Intern role remote, hybrid, or on-site?
This role is on-site, based in Singapore.
How do I apply for this QO Intern role?
You can apply directly on Takeda's careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.