ABOUT TAKEDA SINGAPORE
Takeda's Singapore biologics manufacturing facility produces potentially life-saving medicines for patients with rare blood disorders including Hemophilia A and B.
This site is Takeda's only biologics drug substance manufacturing facility in Asia. It is part of the company's global Biologics Operating Unit network.
The facility includes two buildings with manufacturing suites and laboratories. In 2022, it became Takeda's first positive energy building, certified by Singapore's Building and Construction Authority's Green Mark scheme.
JOB DETAILS
Position: Biotechnologist III
Location: Woodlands, Singapore
Department: Biologics Manufacturing
Employment Type: Regular, Full-time
Work Schedule: 12-hour rotating shifts, including holidays and overtime as required
Reporting To: Manufacturing Supervisor or Team Lead
THE ROLE
The Biotechnologist III performs routine and critical manufacturing operations in Cell Culture and Purification areas under general supervision. You will operate production equipment according to Standard Operating Procedures for commercial and clinical products.
This is a hands-on manufacturing role in a cGMP environment. You will work with bioreactors, purification systems, and process control systems. You will follow written instructions precisely while developing your technical skills through competency-based training.
Work schedules may be adjusted to meet production demands. Flexibility is essential.
PRIMARY RESPONSIBILITIES
Production Operations
Execute routine and critical production operations in Cell Culture and Purification areas. Operate production equipment according to established procedures. Follow instructions in the Electronic Batch Management system, Master Batch Records, and Master Formulation Records where applicable.
Process Monitoring and Control
Attain operating knowledge of the Process Control System. Perform equipment monitoring to ensure proper operation. Record data in logbooks and log-sheets. Review logbooks and log-sheets data for accuracy and completeness.
Laboratory Tasks
Perform basic laboratory tasks including sampling, pH measurements, and conductivity measurements. Demonstrate aseptic technique in handling product and materials where applicable.
Troubleshooting
Troubleshoot and resolve process-related issues as they arise. Initiate and document production events in the Global Event Management System or equivalent. Propose document revisions to improve clarity or accuracy.
Safety and Compliance
Carry out work in a safe manner, notifying management of safety issues and risks. Complete required training on time. Adhere to all applicable EHS requirements.
EQUIPMENT AND FACILITY SUPPORT
Perform scheduled cleaning of equipment according to procedures.
Assist in the assembly and disassembly of process equipment.
Perform standardization of equipment as required.
Perform basic 5S housekeeping in work areas.
Initiate Corrective Work Orders in the C3ME system or equivalent when issues are identified.
TRAINING AND DEVELOPMENT
Meet and maintain all training requirements.
Pursue on-the-job training through Competency Assessments to increase knowledge and understanding.
Develop and maintain a personal development plan.
Provide annual performance self-assessment on development plan progress.
ADDITIONAL RESPONSIBILITIES
Demonstrate commitment to fair and respectful relationships with others.
Behave in accordance with Takeda's Code of Conduct.
Perform any other duties as assigned by supervisor.
QUALIFICATIONS AND EXPERIENCE
Education and Experience Requirements
Applicants with the following qualifications and experience are encouraged to apply:
- Degree in Chemical Engineering, Bioengineering, Chemical & Biomolecular Engineering, Pharmaceutical Engineering or related field with 0-2 years of relevant experience in the biotechnology or pharmaceutical industry
- Diploma in Applied Chemistry, Biomedical Sciences, Chemical Engineering, Food Science & Technology, Biologics & Process Technology, Chemical & Pharmaceutical Technology, Food Science & Nutrition, Molecular Biotechnology, Biotechnology, Chemical & Biomolecular Engineering, Pharmacy Science or related field with 2-4 years of relevant experience in the biotechnology or pharmaceutical industry
- Nitec in Biotechnology, Chemical Process Technology or related field with 4-6 years of relevant experience in the biotechnology or pharmaceutical industry
SKILLS AND COMPETENCIES
Technical Skills
Ability to follow written instructions in the form of Electronic Batch Management, Batch Records, and Standard Operating Procedures. Full awareness of current Good Manufacturing Practices. Proficient documentation and computer skills. Proficient in aseptic technique where applicable. May be required to perform as a subject matter expert for equipment or systems.
Problem-Solving
Possess good troubleshooting skills. Ability to identify and resolve process issues effectively.
Communication
Possess good communication skills. Ability to work effectively with team members and across shifts.
Physical Requirements
Ability to wear personal protective equipment including safety glasses, goggles, gloves, and safety shoes. Ability to gown and gain entry to biotechnology and pharmaceutical manufacturing areas. Ability to work in and out of 2-8°C cold rooms with appropriate PPE if required. Ability to work in confined spaces if required. Ability to work around chemicals including alcohols, acids, and bases.
WORK ENVIRONMENT
Shift Schedule
12-hour rotating shifts. Work on holidays and overtime as required. Schedule may be adjusted to meet production demands.
Physical Demands
Gowning and entry to classified manufacturing areas. Standing for extended periods. Work in cold environments with protective equipment. Potential work in confined spaces.
Chemical Handling
Work with chemicals including alcohols, acids, and bases following established safety procedures.
DEVELOPMENT OPPORTUNITIES
Technical Growth
Deepen your understanding of cell culture and purification operations. Develop proficiency in operating bioreactors, chromatography systems, and process control systems. Build expertise in aseptic technique and cGMP compliance.
Professional Growth
Strengthen troubleshooting and problem-solving abilities. Learn to document work accurately and completely. Develop communication skills for effective teamwork.
Career Progression
Progress through competency assessments to increase knowledge and capabilities. Build foundation for advancement within Takeda's manufacturing organization.
WHY JOIN TAKEDA
Global Leader with Local Impact
Work at Takeda's only biologics drug substance manufacturing facility in Asia. Produce medicines for patients with rare blood disorders worldwide.
State-of-the-Art Facility
Join a world-class facility with two buildings including manufacturing suites and laboratories. Work in Takeda's first positive energy building certified by Singapore's Green Mark scheme.
Commitment to Quality
Maintain the highest standards of cGMP and manufacturing excellence. Produce medicines that patients depend on.
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 contributes to potentially life-saving medicines. Your work directly impacts patient health.
Inclusive Workplace
Takeda is committed to creating a diverse workforce and providing equal employment opportunities to all employees and applicants.
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 your education and any relevant manufacturing experience. Indicate which qualification pathway applies to you. Tell us why you are interested in biopharmaceutical manufacturing at Takeda.
Apply for the Biotechnologist III position at Takeda Singapore - Woodlands.
Takeda is proud to provide equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law.
