Biotechnologist - MFG Suite 1

Join to apply for the
Biotechnologist - MFG Suite 1
role at
Takeda
1 week ago Be among the first 25 applicants
Join to apply for the
Biotechnologist - MFG Suite 1
role at
Takeda
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
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-the-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% - Equipment and facility support
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 Training & Development
Meet and maintain training requirements
Develop and maintain personal development plan
Provide annual performance self-assessment on development plan
Others
Adhere to applicable EHS requirements
Maintain a fair and respectful relationship with others and behave in accordance with Takeda’s Code of Conduct
Perform 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 with 0-2 years relevant experience
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 with 2-4 years relevant experience
Nitec in Biotechnology / Chemical Process Technology or related with 4-6 years relevant experience
Will work holidays and overtime as required
May need to adjust work schedule to meet production demands
Key Skills and Competencies
May serve as a subject matter expert for equipment and systems
Ability to follow written instructions in EBM, Batch Records, and SOPs
Good communication and troubleshooting skills
Knowledge of current Good Manufacturing Practices (cGMP)
Proficient documentation and computer skills
Proficient in aseptic technique where applicable
Ability to wear PPE such as safety glasses, gloves, and safety shoes
Ability to gown and gain entry to manufacturing areas
Ability to work in cold rooms and confined spaces if required
Ability to work around chemicals (alcohols, acids, bases)
More about us:
At Takeda, we are transforming patient care through novel pharmaceuticals and patient support programs. We foster an inclusive, collaborative workplace committed to delivering Better Health and a Brighter Future globally.
Our commitments:
Takeda is dedicated to creating a diverse workforce and providing equal employment opportunities to all employees and applicants, regardless of race, religion, sex, sexual orientation, gender identity, age, disability, or other protected characteristics.
Location:
SGP - Singapore - Woodlands
Worker Type:
Employee
Worker Sub-Type:
Regular
Time Type:
Full time
Seniority level
Entry level
Employment type
Full-time
Job function
Research, Analyst, and Information Technology
Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr