đĄď¸ Be the Guardian of GMP in Biopharmaceutical Manufacturing
Objectives
In this internship, you will join the Quality Assurance Support (QAS) team, providing critical quality oversight to ensure GMP compliance within Takedaâs biopharmaceutical manufacturing operations in Singapore. You will partner directly with the manufacturing team to uphold quality systems, support raw material release, and contribute to procedural excellence.
đ Location:Â SGP - Singapore - Woodlands
đ¨âđŹ Worker Type: Paid Intern (Fixed Term Trainee)
â° Time Type:Â Full time
đ RESPONSIBILITIES
đ Quality Oversight
- Act as a member of the QAS team, providing on-floor quality oversight in the manufacturing suite.
- Partner with manufacturing to ensure adherence to GMP requirements and quality systems.
- Participate in cross-functional meetings to share learnings and align on best practices.
- Support compliance, regulatory, and inspection readiness activities as needed.
đŚ QA Support Operations
- Assist in the timely release of raw materials to support production schedules.
- Manage raw material reference samples and associated documentation.
- Support the manufacturing team with quality-related queries, interpretations, and issue resolution.
- Contribute to the development and writing of SOPs and master batch records, ensuring compliance with good documentation practices (GDP) and regulatory standards.
đ Additional Responsibilities
- Perform timely archival of QA Support documents.
- Build strong partnerships across departments to foster open communication and collaboration.
- Adhere to all EHS requirements and Takedaâs Code of Conduct.
đ¤ EDUCATION AND EXPERIENCE REQUIREMENTS
- Background in Chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences, or an equivalent field.
- Keen interest in pursuing a career in the biopharmaceutical industry.
- Proficiency in Microsoft Office.
- No prior experience requiredâstructured training and mentorship will be provided.
đ KEY SKILLS AND COMPETENCIES
- Committed & Positive:Â Motivated mindset with flexibility to adapt to dynamic environments.
- Strong Communicator:Â Excellent interpersonal, verbal, and written communication skills.
- Collaborative Team Player:Â Ability to work effectively within cross-functional teams.
- Emotional Intelligence:Â Good emotional handling and relationship-building skills.
- Organized & Proactive:Â Strong time management and attention to detail.
đź WHY JOIN THIS INTERNSHIP?
- Hands-On GMP Experience: Gain direct exposure to quality systems, manufacturing oversight, and compliance in a world-class biopharma facility.
- Cross-Functional Insight: Work at the intersection of QA, Manufacturing, and Supply Chain.
- Mentorship & Development:Â Learn from experienced QA professionals in a supportive, structured environment.
- Career Pathway: Build a foundation for roles in Quality Assurance, Compliance, Manufacturing, or Regulatory Affairs.
- Paid Opportunity:Â Receive competitive compensation while developing in-demand industry skills.
đŻ IDEAL FOR STUDENTS IN:
- Pharmaceutical Sciences / Biotechnology
- Chemistry / Biochemistry
- Quality Assurance / Regulatory Affairs
- Chemical Engineering / Life Sciences
đ READY TO UPHOLD QUALITY IN BIOPHARMA MANUFACTURING?
đ APPLY NOW FOR THE QUALITY ASSURANCE SUPPORT INTERNSHIP IN SINGAPORE.
Takeda is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
