Manufacturing Biotechnologist III
Takeda | Singapore | Biologics Manufacturing
ABOUT THE ROLE
The Manufacturing Biotechnologist III is focused on converting raw materials and components into finished biopharmaceutical products. This role involves general production work, assembling components, processing batches of materials, operating machine tools, and packaging finished goods.
You will support Takeda's mission by ensuring efficient and high-quality production processes at our Woodlands facility in Singapore.
This is a fixed-term, full-time position.
POSITION DETAILS
Role: Manufacturing Biotechnologist III
Company: Takeda
Location: Singapore - Woodlands
Department: Manufacturing
Employment Type: Fixed Term (Full-time)
Worker Sub-Type: Fixed Term
Level: Experienced individual contributor
Supervision: General supervision, works independently within established procedures
WHY THIS ROLE EXISTS
Biopharmaceutical manufacturing transforms scientific discoveries into medicines that patients depend on. Before a therapy reaches a patient, it must be manufactured—batch after batch, with unwavering quality and consistency.
The Manufacturing Biotechnologist III performs this essential work.
You will operate equipment, process materials, assemble components, and package finished goods. You will work within cGMP regulations and follow established procedures to ensure every product meets Takeda's quality standards. Your attention to detail and technical skill directly impacts patient safety.
WHAT YOU WILL DO
Production Manufacturing
Perform general production manufacturing work in a cGMP environment. Process manufacturing batches of bulk materials and ingredients according to established procedures. Set up and operate machine tools to convert materials into parts, sub-assemblies, and assemblies.
Assembly and Finishing
Assemble finished components or parts into finished products. Conduct surface finishing of parts, components, and assembled items as required. Ensure all assemblies meet quality specifications.
Packaging
Package materials and finished goods into appropriate containers for protection, display, and handling. Follow packaging specifications and ensure proper labeling and documentation.
Equipment Operation
Set up and operate production equipment. Perform routine equipment checks and maintenance. Troubleshoot production issues effectively to minimize downtime and maintain workflow continuity.
Quality and Compliance
Apply Good Manufacturing Practices independently in routine and moderately complex situations. Conduct Quality Control assessments to ensure products meet strict standards. Utilize Product and Manufacturing Information to enhance production quality and efficiency.
Continuous Improvement
Implement Continuous Improvement Process strategies to optimize production workflows. Apply lean manufacturing principles to reduce waste and increase production efficiency. Collaborate with teams across departments to achieve production goals and improve processes.
Safety
Manage safety protocols to ensure a secure working environment for all staff. Follow all safety requirements and report any concerns promptly.
Planning and Execution
Plan and execute production schedules to meet targets and optimize resource use. Work with team members to ensure smooth operations across shifts.
SKILLS AND QUALIFICATIONS
Core Competencies
Good Manufacturing Practices
Apply GMP independently in routine and moderately complex situations with minimal guidance. Understand the principles behind the procedures and why they matter.
Product and Manufacturing Information
Utilize PMI effectively to enhance production quality and efficiency. Access and apply manufacturing information correctly.
Continuous Improvement
Implement process improvement strategies to optimize workflows. Contribute to a culture of ongoing enhancement.
Quality Control
Conduct quality assessments independently. Ensure products meet established standards before release.
Troubleshooting
Identify and resolve production issues effectively. Minimize downtime and maintain workflow continuity.
Collaboration
Work with teams across departments to achieve production goals. Communicate effectively to facilitate smooth operations.
Equipment Maintenance
Maintain and troubleshoot equipment to ensure operational efficiency and safety. Perform routine checks and escalate issues as needed.
Production Planning
Plan and execute production schedules to meet targets. Optimize resource use within your area of responsibility.
Safety Management
Follow and contribute to safety protocols. Maintain a secure working environment.
Lean Manufacturing
Apply lean principles to reduce waste and increase efficiency. Identify opportunities for improvement.
Attention to Detail
Pay close attention to details, ensuring high-quality production outputs. Catch errors before they become problems.
Communication
Communicate effectively with team members and across departments. Facilitate smooth operations through clear information sharing.
EXPERIENCE AND EDUCATION
Education
High school diploma and any necessary certifications will prepare you for this role.
Experience
Some relevant working experience in manufacturing, production, or a related environment.
Level Description
At this level you will utilize and expand your working knowledge and skills. This role requires broadened technical abilities to perform a diverse set of activities, working within established procedures under general supervision.
You will be responsible for evaluating and selecting solutions, with errors potentially causing moderate impact but being correctable. Your interactions will extend beyond your department, contributing to a collaborative work environment.
WHAT YOU WILL LEARN AND DEVELOP
Technical Skills
Deepen your understanding of cGMP manufacturing. Develop proficiency in equipment operation and troubleshooting. Build expertise in quality control and continuous improvement.
Professional Skills
Strengthen your collaboration and communication abilities. Learn to work effectively across departments. Develop your capacity to plan and execute production schedules.
Personal Growth
Build confidence in independent decision-making within established procedures. Expand your ability to evaluate and select solutions. Contribute to a culture of quality and continuous improvement.
A TYPICAL SHIFT MIGHT INCLUDE
Start of Shift
Receive handover from previous shift. Review production schedule and priorities for the day. Check equipment status and materials availability.
During Shift
Set up and operate production equipment according to batch records. Process materials following established procedures. Monitor equipment and processes for any issues. Perform in-process quality checks. Document all activities accurately and completely.
Mid-Shift
Troubleshoot a minor equipment issue, resolving it quickly to minimize downtime. Communicate with the team lead about production status.
End of Shift
Complete batch documentation. Clean and prepare equipment for next shift. Provide clear handover to incoming team. Report any safety observations or equipment concerns.
WHY TAKEDA
Global Leader
Takeda is a values-driven biopharmaceutical leader with approximately 50,000 employees across 80 countries. Our mission is to deliver Better Health and a Brighter Future for patients around the world.
Commitment to Quality
We maintain the highest standards of cGMP and manufacturing excellence. You will learn what it means to produce medicines that patients depend on.
Singapore Operations
Takeda's Woodlands facility is a key part of our global manufacturing network. You will work at a world-class site with state-of-the-art equipment and processes.
Career Foundation
This role offers the opportunity to build deep expertise in biopharmaceutical manufacturing. Whether you are early in your career or developing new skills, you will gain experience that is essential across the industry.
Collaborative Environment
Work alongside experienced manufacturing professionals who support your success. Contribute to a team that values quality, safety, and continuous improvement.
Purpose-Driven Work
Every batch you produce, every component you assemble, every product you package contributes to medicines that improve and save lives. Your work matters.
WHAT WE OFFER
Opportunity to work with a global biopharmaceutical leader
Hands-on experience in cGMP manufacturing
Supportive and collaborative team environment
Professional development and skill-building
Purpose-driven work that impacts patient health
Fixed-term position with full-time hours
APPLICATION PROCESS
Submit your application through the Takeda careers portal.
The hiring team reviews all submissions.
Qualified candidates are contacted for an initial conversation.
Interviews are conducted with manufacturing leadership.
Decisions and offers are communicated in a timely manner.
TO APPLY
Please submit your resume highlighting any manufacturing or production experience. Include a brief note on why you are interested in biopharmaceutical manufacturing. Tell us what interests you about Takeda.
Apply for the Manufacturing Biotechnologist III position at Takeda Singapore.
Takeda is an equal opportunity employer committed to diversity and inclusion. We welcome applications from all qualified candidates. If you need accommodations during the application process, please let us know.
