About the role
AI summarisedBiotechnologist III at Takeda's biologics manufacturing facility in Singapore, responsible for routine and critical manufacturing operations in Cell Culture and Purification areas. The role involves operating production equipment per SOPs, executing batch records, performing equipment monitoring, and supporting facility projects. Requires a degree or diploma in relevant fields with up to 6 years of experience in biotech or pharma, and knowledge of cGMP.
BiopharmaFull-timeManufacturing/Production
Key Responsibilities
- 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
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
- May be required to perform as a subject matter expert for equipment and/or systems
- Ability to following 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)