Biotechnologist III

Takeda; Singapore; On-site; SGD 20,000 - 60,000; Full time

Job summary

A global biopharmaceutical company seeks a Biotechnologist III for its Woodlands, Singapore facility. The role includes executing manufacturing operations in a cGMP environment, performing critical tasks in Cell Culture and Purification. Ideal candidates should have relevant education and experience in biotechnology or related fields, along with strong communication and troubleshooting skills. The position may require overtime and adaptation to production demands.

Qualifications

• 0-2 years of experience in biotechnology or pharmaceutical industry required.
• Willingness to work holidays and overtime as needed.

Responsibilities

• Execute routine and critical production operations.
• Perform basic laboratory tasks including sampling and pH measurements.
• Troubleshoot and resolve process-related issues.

Skills

Troubleshooting skills

Communication skills

Knowledge of cGMP

Education

Degree in relevant engineering field

Diploma in related field

Nitec in Biotechnology

Job description

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.

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.

Responsibilities:

The individual will be responsible for:

• Execution of routine and critical production operations
• Learning and performing well-defined SOPs
• Pursuing on-the-job training through Competency Assessments to increase knowledge and understanding
• Executing instructions and recording data in the Electronic Batch Management (EBM) system if applicable
• Executing instructions and recording data in the Master Batch Records (MBRs) and Master Formulation Records (MFRs) if applicable
• Attaining operating knowledge of the Process Control System (PCS)
• Recording data into logbooks and log-sheets
• Reviewing logbooks and log-sheets data
• Performing equipment monitoring
• Performing basic laboratory tasks including but not limited to sampling, pH and conductivity measurements
• Demonstrating aseptic technique in the handling of product and materials if applicable
• Troubleshooting and resolving process related issues
• Initiating and documenting production events in the Global Event Management System (GEMS) or equivalent system
• Proposing document revisions
• Completing required training on time
• Carrying out work in a safe manner, notifying management of safety issues and risks

The individual will also manage equipment and support facility related projects by:

• Performing scheduled cleaning of equipment
• Assisting in the assembly and disassembly of process equipment
• Performing standardization of equipment
• Performing basic 5S housekeeping
• Initiating Corrective Work Orders in the C3ME system or equivalent system

Requirements:

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 holidays and overtime as required (12 hours shift rotating)
• May be required to adjust work schedule to meet production demands

Key Skills and Competencies

• Ability 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 deg 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)

Diversity and Inclusion:

Takeda is proud of its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment 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.