Biotechnologist III

TAKEDA PHARMACEUTICALS AMERICA, INC.; Singapore; On-site; SGD 20,000 - 60,000; Full time

Job summary

A leading global biopharmaceutical company in Singapore is seeking a Biotechnologist III to perform critical manufacturing operations. You will execute production duties in cell culture and purification, contributing to therapies for patients suffering from rare blood disorders. The ideal candidate has relevant experience in biotechnology or pharmaceutical fields, with an emphasis on safety and quality practices.

Benefits

Global Top Employer certification

Inclusive and collaborative workplace

Opportunity for personal development

Qualifications

• 0-2 years of relevant experience in the biotechnology or pharmaceutical industry.
• Experience in manufacturing operations is a plus.
• Will work 12-hour shifts including weekends and overtime as required.

Responsibilities

• Perform routine and critical production operations.
• Maintain accurate production records in EBM and MBRs.
• Troubleshoot process-related issues.

Skills

Communication skills

Troubleshooting skills

Good Manufacturing Practices

Documentation skills

Aseptic technique

Education

Degree in Chemical Engineering or related

Diploma in Applied Chemistry or related

Nitec in Biotechnology or related

Job description

Skills

On the Global Manufacturing and Supply (GMS) team at Takeda, you’ll be part of a rapidly transforming industry that’s applying technology and data in new ways. Within our agile, innovative, people‑centric organization, your work will matter every day as you use your skills to help us manufacture therapies for patients on our four platforms:

• Small Molecules
• Biologics
• Plasma

As part of the GMS team, you’ll have the opportunity to pursue unique experiences and build new skills, and you’ll know that the work you do every day makes an impact — on our patients, our people, our planet, and on yourself.

Job ID R0168899 | Date posted 11/24/2025 | Location Singapore, Singapore

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Job Description

Company Profile

Takeda’s Singapore biologics manufacturing facility focuses on manufacturing potentially life‑saving medicines for patients suffering from rare blood disorders such as Hemophilia A and B. As part of the company’s Biologics Operating Unit network, the site is Takeda’s only biologics drug substance manufacturing facility in Asia. The facility has two buildings, including manufacturing suites and laboratories, as well as Takeda’s first positive energy building certified by Singapore’s Building and Construction Authority’s Green Mark scheme in 2022.

Job Title: Biotechnologist III

Location: Woodlands, Singapore

About The Role

With general supervision the individual will perform routine and critical manufacturing operations, including but not limited to work functions in Cell Culture and Purification areas. Operates production equipment according to Standard Operating Procedures (SOPs) for the production of commercial and/or clinical products.

How You Will Contribute

80% - Primary responsibilities include:

• Execution of routine and critical production operations
• Learn and perform well‑defined SOPs
• Pursue on‑job training through Competency Assessments to increase knowledge and understanding
• Execute instructions and record data in the Electronic Batch Management (EBM) system if applicable
• Execute instructions and record data in the Master Batch Records (MBRs) and Master Formulation Records (MFRs) if applicable
• Attain operating knowledge of the Process Control System (PCS)
• Record data into logbooks and log‑sheets
• Review logbooks and log‑sheets data
• Perform equipment monitoring
• Perform basic laboratory tasks including but not limited to sampling, pH and conductivity measurements
• Demonstrate aseptic technique in the handling of product and materials if applicable
• Troubleshoot and resolve process related issues
• Initiate and document production events in the Global Event Management System (GEMS) or equivalent system
• Propose document revisions
• Complete required training on time
• Carry out work in a safe manner, notifying management of safety issues and risks

10% - The individual will manage equipment and support facility related projects by:

• Perform scheduled cleaning of equipment
• Assist in the assembly and disassembly of process equipment
• Perform standardization of equipment
• Perform basic 5S housekeeping
• Initiate Corrective Work Orders in the C3ME system or equivalent system

10% - Staff Technical Training and Development:

• Meet and maintain training requirements
• Develop and maintain personal development plan
• Provide annual performance self‑assessment on development plan

Others

• 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

What You Bring To Takeda

Education and Experience Requirements

• Degree in Chemical Engineering / Bioengineering / Chemical & Biomolecular Engineering / Pharmaceutical Engineering or related and possess 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 and possess 2‑4 years of relevant experience in the biotechnology or pharmaceutical industry
• Nitec in Biotechnology / Chemical Process Technology or related with 4‑6 years of relevant experience in the biotechnology, pharmaceutical industry
• Will work 12‑hour shift rotating including weekends, public holidays and overtime as required
• May be required to adjust work schedule to meet production demands

Key Skills and Competencies

• May be required to perform as a subject matter expert for equipment and/or systems
• Ability to follow written instructions in the form of Electronic Batch Management (EBM), Batch Records (MBRs, MFRs) and Standard Operating Procedures (SOPs) where applicable
• Possess good communication skills
• Possess good troubleshooting skills
• Full awareness of current Good Manufacturing Practices (cGMP)
• Proficient documentation and proficient computer skills
• Proficient in aseptic technique where applicable
• Ability to wear personal protective equipment such as safety glasses/goggles, gloves and safety shoes
• Ability to gown and gain entry to biotechnology/pharmaceutical manufacturing areas.
• Ability to work in and out of 2‑8 °C Cold Rooms with appropriate personal protective equipment if required
• Ability to work in confined spaces if required
• Ability to work around chemicals (alcohols, acids & bases)

More About Us

At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programmes. Takeda is a patient‑focused company that will inspire and empower you to grow through life‑changing work.

Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

Empowering Our People To Shine

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, colour, 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.

Locations

SGP - Singapore - Woodlands

Worker Type

Employee

Worker Sub‑Type

Fixed Term (Fixed Term)

Time Type

Full time

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