QA Support Intern

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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

Worker Type

Worker Sub-Type

Time Type