216 Manufacturing Team Lead jobs in Singapore
Manufacturing Lead
Posted 4 days ago
Job Viewed
Job Description
The Opportunity
Esco Lifesciences Group is Singapore’s most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 42 locations and 26 direct countries across North America, Europe, Asia, Oceania.
Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first incorporated in 2017.
Esco Aster is a contract research development and manufacturing organization founded and deeply rooted by scientists enabling fellow scientists to translate their bench work into commercially available products at affordable prices.
Our scientific work is in emerging and frontier biology utilizing cells as a final product or deriving products from cells which often we use cells as the factory to derive our target product.
Our first commercial breakthrough success is Esco Aster is commercially first in class being first in the world to be certified for cultivated/cell-based meat to FSSC 22000 and by a competent food regulatory body.
We are first in the region to operate an end-to-end integrated full cell line creation/immortalization or engineered cell line, cell culture process development, analytical development for stem cells and exosomes with full cGMP Capabilities from Drug Substance and small-scale fill & finish for final Cell Therapy Product.
The work we do creates a remarkable and lasting impact on our world. We offer you an opportunity to be part of this exciting journey to own your career and firsthand exposure to new emerging modalities supporting translational sciences.
Join us as we redefine BioSolutions for One World and One Health for the current and future generations to come.
Esco Aster.
One World Biosolutions for One Health.
Who we’re looking for
Physical / Mental Requirements / Work Environment:
- Strong leadership and communication skills.
- Ability to stay focused under pressure and adapt proactively.
- Critical thinker with a systematic and meticulous approach.
- Curious and self-motivated to stay updated on cell/gene therapy and emerging technologies.
- Committed to safety, quality, compliance, and timely delivery.
- Cleanroom and GMP manufacturing settings.
- Requires standing for long periods, working with sterile systems, and wearing full gowning/PPE.
- May engage in overtime during campaign activities or urgent troubleshooting.
The Scope
To lead and manage the successful technology transfer, manufacturing execution, and commercial readiness of cell and gene therapy products in a cGMP environment, ensuring compliance, efficiency, and delivery excellence throughout the product lifecycle.
Primary work location: Ayer Rajah Crescent, Singapore
Job Responsibilities
- Lead cross-functional biotechnicians and act as the bridge between process development and manufacturing.
- Collaborate with internal/external stakeholders including QA, QC, MSAT, and commercial teams.
- Serve as Manufacturing Subject Matter Expert (SME) during audits, inspections, and due diligence.
- Manage end-to-end technology transfers (internal and external).
- Involve in commissioning, qualification (C&Q) activities.
- Oversee execution of Process Performance Qualification (PPQ), Aseptic Process Simulations (APS), and engineering/pilot runs.
- Oversee cell culture, purification, and fill-finish operations in a single-use, aseptic, cGMP facility.
- Ensure readiness of raw materials, equipment, and team for autologous/allogeneic campaigns.
- Monitor, document, and troubleshoot manufacturing activities, ensuring compliance with SOPs and regulatory requirements.
- Author, review, and manage cGMP documentation: SOPs, batch records, risk assessments, protocols, etc.
- Lead manufacturing change control, deviation investigations and implement CAPAs.
- Lead the implementation of electronic batch records.
- Potentially leading a small team.
- Undertake other tasks as assigned by the management based on project needs.
Requirements
- Minimum Bachelor’s Degree in Biotechnology related disciplines, Chemical Engineering, Pharmaceutical Science or relevant discipline with 2 years or more experience in a cGMP/aseptic environment in biologics or cell and gene therapy.
- Minimum of 4-6 years in cGMP Biologics or cell and gene therapy manufacturing with relevant industry knowledge, hands on equipment experience and technical expertise.
- Strong knowledge of cGMP practices and global regulatory requirements such as USFDA GMP, EU GMP, HSA GMP and PIC/S GMP.
- In-depth knowledge of the drug development process and commercialization pathways.
- Proficient in MS Office Suite (Microsoft Word, PowerPoint, Excel).
- Able to work independently and task oriented in a dynamic environment.
- Strong team player with a strong set of interpersonal skills.
- Excellent written and verbal communication skills.
- Experience in bringing cell and gene therapy products through clinical development to market is an added advantage.
- Proven track record in regulatory strategy and interactions is an added advantage.
- Proficient in MS Office Suite (Microsoft Word, PowerPoint, Excel).
- Able to work independently and task oriented in a dynamic environment.
- Strong team player with a strong set of interpersonal skills.
- Excellent written and verbal communication skills.
Apply now by submitting a Cover Letter and CV to .
Manufacturing Lead Engineer - Listed SEMICON
Posted today
Job Viewed
Job Description
Responsibilities:
Lead and supervise a team of manufacturing operators to ensure smooth and efficient production operations.
Monitor production schedules and targets, and take corrective actions as needed to meet customer requirements.
Train new employees on safety procedures, equipment operation, and manufacturing processes.
Develop and implement standard operating procedures (SOPs) to ensure consistent quality and productivity.
Coordinate with other departments to ensure timely availability of materials and resources for production.
Perform regular inspections to ensure adherence to quality standards and identify areas for improvement.
Effectively communicate with team members, management, and cross-functional teams to address any issues and drive continuous improvement.
Ensure compliance with company policies, safety regulations, and industry standards.
Diploma or Degree in Engineering or related field.
With 2 years of experience in the wafer fab/ semiconductor industry.
Prior experience in a leadership or team lead role.
Ability to lead and motivate a team in a fast-paced environment.
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Manufacturing Shift Lead
Posted 6 days ago
Job Viewed
Job Description
**Job Description**
**About the role:**
This position is required perform with minimal 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. Will support or lead engineering and validation activities. Deputy to the Shift Supervisor, acting on Supervisor's behalf when needed. The individual will deliver excellence in manufacturing processing and provide support in integrate best practices, where appropriate, into manufacturing.
**How you will contribute:**
Primary Responsibility
+ Execution of all routine and critical operations in both Upstream and Downstream or both Equipment Prep and Buffer Prep areas. Perform commissioning and validation activities in respective areas.
+ Active participation in troubleshooting. Collaborate with Shift Supervisor, SME and Manufacturing Leadership for issue resolution.
+ Serve as deputy for Shift Supervisor and acting Supervisor during Supervisor absences
+ Monitor material consumption and coordinate all materials deliveries
+ Learn and perform well-defined SOPs in all areas of responsibility
+ 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
+ Review manufacturing documentation and EBM or PCS alerts real-time to ensure compliance if applicable
+ Attain operating knowledge of the Process Control System (PCS)
+ Record data into logbooks and log-sheets
+ Review logbooks and log-sheets data
+ Ensure documentation is complete, reviewed and meets good documentation practices (forms, logbooks, EBM, batch records, etc.)
+ Perform equipment monitoring
+ Perform and coordinate basic laboratory tasks including but not limited to sampling, pH and conductivity measurements
+ Demonstrate aseptic technique in the handling of product and materials
+ Informing management of events impacting production schedule
+ Propose and review document revisions
+ Recommend/Implement process changes/improvements or safety/ergonomic improvements.
+ Complete required training on time
+ Carry out work in a safe manner, notifying management of safety issues and risks
Quality
+ Lead and participate in investigations of production events in the Global Event Management System (GEMS) or equivalent systems and work with cross-functional departments to identify root causes.
+ Complete action items for event investigations
+ Implement appropriate CAPAs from event investigations
+ Review document revisions of Standard Operating Procedures/Batch Records
+ Communicate any quality issues/concerns to Supervisor and QA
+ Implement Change Controls for production
Staff Technical Training and Development
+ Meet and maintain training requirements
+ Develop and maintain personal development plan
+ Provide annual performance self-assessment on development plan
General Responsibilities:
+ Act as a role model (Lead by Example)
+ Act as a Subject Matter Expert SME for improvement projects
+ Act as a resource / SME for staff
+ Provide technical training for area personnel and assess training effectiveness
+ Develop training material for technical training
+ Assess staff skill sets and provide feedback to Supervisor
+ Perform scheduled cleaning of equipment
+ Assist in the assembly and disassembly of process equipment
+ Perform standardization of equipment
+ Perform basic 5S housekeeping
Initiate and follow up on Corrective Work Orders in the C3ME system or equivalent system
+ Support change over activities
+ 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 possesses more than 4 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 more than 6 years of relevant experience in the biotechnology or pharmaceutical industry
+ Nitec in Biotechnology / Chemical Process Technology or related with more than 8 years of relevant experience in the biotechnology, pharmaceutical industry.
+ Excellent self-motivated team player with hands-on attitude and good communication skills
+ Able to work on 12 hours rotating shift
+ Will work holidays and overtime as required
+ May be required to adjust work schedule to meet production demands
**Key Skills and Competencies**
+ Will be required to perform as a subject matter expert for equipment and/or systems
+ Knowledge of cGMP's and applicable agency regulations (such as the FDA, EMEA) to ensure inspection readiness of department.
+ Proficient at following written instructions in the form of Electronic Batch Management (EBM), Batch Records (MBRs, MFRs) and Standard Operating Procedures (SOPs) where applicable
+ Self-motivated individual with the ability to complete and manage multiple floor activities in an effective and compliant manner. In the absence of the supervisor, they are the person of authority.
+ Expected to act on behalf of the supervisor while on the floor
+ Demonstrates appropriate level of adaptability, maintains positive outlook, and demonstrates composure under pressure.
+ Possess excellent communication skills to all levels throughout the organization
+ Possess excellent troubleshooting skills
+ Proficient documentation and proficient computer skills
+ Proficient in aseptic technique where applicable
+ Proficient as a system user of business systems such as C3ME and Trackwise
+ 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)
**More about us:**
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. 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, 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._
**Locations**
SGP - Singapore - Woodlands
**Worker Type**
Employee
**Worker Sub-Type**
Regular
**Time Type**
Full time
Manufacturing Shift Lead
Posted today
Job Viewed
Job Description
About the role:
This position is required perform with minimal 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. Will support or lead engineering and validation activities. Deputy to the Shift Supervisor, acting on Supervisor's behalf when needed. The individual will deliver excellence in manufacturing processing and provide support in integrate best practices, where appropriate, into manufacturing.
How you will contribute:
Primary Responsibility
- Execution of all routine and critical operations in both Upstream and Downstream or both Equipment Prep and Buffer Prep areas. Perform commissioning and validation activities in respective areas.
- Active participation in troubleshooting. Collaborate with Shift Supervisor, SME and Manufacturing Leadership for issue resolution.
- Serve as deputy for Shift Supervisor and acting Supervisor during Supervisor absences
- Monitor material consumption and coordinate all materials deliveries
- Learn and perform well-defined SOPs in all areas of responsibility
- 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
- Review manufacturing documentation and EBM or PCS alerts real-time to ensure compliance if applicable
- Attain operating knowledge of the Process Control System (PCS)
- Record data into logbooks and log-sheets
- Review logbooks and log-sheets data
- Ensure documentation is complete, reviewed and meets good documentation practices (forms, logbooks, EBM, batch records, etc.)
- Perform equipment monitoring
- Perform and coordinate basic laboratory tasks including but not limited to sampling, pH and conductivity measurements
- Demonstrate aseptic technique in the handling of product and materials
- Informing management of events impacting production schedule
- Propose and review document revisions
- Recommend/Implement process changes/improvements or safety/ergonomic improvements.
- Complete required training on time
- Carry out work in a safe manner, notifying management of safety issues and risks
Quality
- Lead and participate in investigations of production events in the Global Event Management System (GEMS) or equivalent systems and work with cross-functional departments to identify root causes.
- Complete action items for event investigations
- Implement appropriate CAPAs from event investigations
- Review document revisions of Standard Operating Procedures/Batch Records
- Communicate any quality issues/concerns to Supervisor and QA
- Implement Change Controls for production
Staff Technical Training and Development
- Meet and maintain training requirements
- Develop and maintain personal development plan
- Provide annual performance self-assessment on development plan
General Responsibilities:
- Act as a role model (Lead by Example)
- Act as a Subject Matter Expert SME for improvement projects
- Act as a resource / SME for staff
- Provide technical training for area personnel and assess training effectiveness
- Develop training material for technical training
- Assess staff skill sets and provide feedback to Supervisor
- Perform scheduled cleaning of equipment
- Assist in the assembly and disassembly of process equipment
- Perform standardization of equipment
- Perform basic 5S housekeeping
Initiate and follow up on Corrective Work Orders in the C3ME system or equivalent system
- Support change over activities
- 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 possesses more than 4 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 more than 6 years of relevant experience in the biotechnology or pharmaceutical industry
- Nitec in Biotechnology / Chemical Process Technology or related with more than 8 years of relevant experience in the biotechnology, pharmaceutical industry.
- Excellent self-motivated team player with hands-on attitude and good communication skills
- Able to work on 12 hours rotating shift
- Will work holidays and overtime as required
- May be required to adjust work schedule to meet production demands
Key Skills and Competencies
- Will be required to perform as a subject matter expert for equipment and/or systems
- Knowledge of cGMP's and applicable agency regulations (such as the FDA, EMEA) to ensure inspection readiness of department.
- Proficient at following written instructions in the form of Electronic Batch Management (EBM), Batch Records (MBRs, MFRs) and Standard Operating Procedures (SOPs) where applicable
- Self-motivated individual with the ability to complete and manage multiple floor activities in an effective and compliant manner. In the absence of the supervisor, they are the person of authority.
- Expected to act on behalf of the supervisor while on the floor
- Demonstrates appropriate level of adaptability, maintains positive outlook, and demonstrates composure under pressure.
- Possess excellent communication skills to all levels throughout the organization
- Possess excellent troubleshooting skills
- Proficient documentation and proficient computer skills
- Proficient in aseptic technique where applicable
- Proficient as a system user of business systems such as C3ME and Trackwise
- 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)
More about us:
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. 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, 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.
Tell employers what skills you havePharmaceutical Industry
FDA
5S
Upstream
Cell Culture
Biologics
Purification
Manufacturing Operations
Biotechnology
Technical Training
Food Science
Biological sciences
Nutrition
Process Control
Chemical Engineering
Manufacturing Shift Lead
Posted today
Job Viewed
Job Description
1 month ago Be among the first 25 applicants
Get AI-powered advice on this job and more exclusive features.
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
Cell and Gene
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.
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Job ID
R
Date posted
07/04/2025
Location
Singapore, Singapore
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 Noticeand 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
About the role:
This position is required perform with minimal 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. Will support or lead engineering and validation activities. Deputy to the Shift Supervisor, acting on Supervisor’s behalf when needed. The individual will deliver excellence in manufacturing processing and provide support in integrate best practices, where appropriate, into manufacturing.
How You Will Contribute
Primary Responsibility
Execution of all routine and critical operations in both Upstream and Downstream or both Equipment Prep and Buffer Prep areas. Perform commissioning and validation activities in respective areas.
Active participation in troubleshooting. Collaborate with Shift Supervisor, SME and Manufacturing Leadership for issue resolution.
Serve as deputy for Shift Supervisor and acting Supervisor during Supervisor absences
Monitor material consumption and coordinate all materials deliveries
Learn and perform well‐defined SOPs in all areas of responsibility
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
Review manufacturing documentation and EBM or PCS alerts real‐time to ensure compliance if applicable
Attain operating knowledge of the Process Control System (PCS)
Record data into logbooks and log‐sheets
Review logbooks and log‐sheets data
Ensure documentation is complete, reviewed and meets good documentation practices (forms, logbooks, EBM, batch records, etc.)
Perform equipment monitoring
Perform and coordinate basic laboratory tasks including but not limited to sampling, pH and conductivity measurements
Demonstrate aseptic technique in the handling of product and materials
Informing management of events impacting production schedule
Propose and review document revisions
Recommend/Implement process changes/improvements or safety/ergonomic improvements.
Complete required training on time
Carry out work in a safe manner, notifying management of safety issues and risks
Quality
Lead and participate in investigations of production events in the Global Event Management System (GEMS) or equivalent systems and work with cross‐functional departments to identify root causes.
Complete action items for event investigations
Implement appropriate CAPAs from event investigations
Review document revisions of Standard Operating Procedures/Batch Records
Communicate any quality issues/concerns to Supervisor and QA
Implement Change Controls for production
Staff Technical Training and Development
Meet and maintain training requirements
Develop and maintain personal development plan
Provide annual performance self‐assessment on development plan
General Responsibilities
Act as a role model (Lead by Example)
Act as a Subject Matter Expert (SME) for improvement projects
Act as a resource / SME for staff
Provide technical training for area personnel and assess training effectiveness
Develop training material for technical training
Assess staff skill sets and provide feedback to Supervisor
Perform scheduled cleaning of equipment
Assist in the assembly and disassembly of process equipment
Perform standardization of equipment
Perform basic 5S housekeeping
Initiate and follow up on Corrective Work Orders in the C3ME system or equivalent system
Support change over activities
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 possesses more than 4 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 more than 6 years of relevant experience in the biotechnology or pharmaceutical industry
Nitec in Biotechnology / Chemical Process Technology or related with more than 8 years of relevant experience in the biotechnology, pharmaceutical industry.
Excellent self‐motivated team player with hands‐on attitude and good communication skills
Able to work on 12 hours rotating shift
Will work holidays and overtime as required
May be required to adjust work schedule to meet production demands
Key Skills And Competencies
Will be required to perform as a subject matter expert for equipment and/or systems
Knowledge of cGMP’s and applicable agency regulations (such as the FDA, EMEA) to ensure inspection readiness of department.
Proficient at following written instructions in the form of Electronic Batch Management (EBM), Batch Records (MBRs, MFRs) and Standard Operating Procedures (SOPs) where applicable
Self‐motivated individual with the ability to complete and manage multiple floor activities in an effective and compliant manner. In the absence of the supervisor, they are the person of authority.
Expected to act on behalf of the supervisor while on the floor
Demonstrates appropriate level of adaptability, maintains positive outlook, and demonstrates composure under pressure.
Possess excellent communication skills to all levels throughout the organization
Possess excellent troubleshooting skills
Proficient documentation and proficient computer skills
Proficient in aseptic technique where applicable
Proficient as a system user of business systems such as C3ME and Trackwise
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 programs. 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, 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.
Locations
SGP - Singapore - Woodlands
Worker Type
Employee
Worker Sub‐Type
Regular
Time Type
Full time
Apply Now
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Seniority level
Mid‐Senior level
Employment type
Full‐time
Job function
Management and Manufacturing
Industries
Pharmaceutical Manufacturing
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Manufacturing Engineering Lead
Posted today
Job Viewed
Job Description
Join to apply for the
Manufacturing Engineering Lead
role at
LionsBot International
Company overview
LionsBot is an international robotics scaleup dedicated to transforming the cleaning and facility services industry. We value ingenuity, problem-solving, adaptability, and an entrepreneurial spirit. As we continue expanding globally, we seek a dynamic Manufacturing Engineer Lead to manage a team of engineers to take charge of all the improvements in the Production Floor. The candidate ensures we have operational excellence and a world-class assembly floor. Deliver top quality robots to meet sales orders and maintain the quality our customers expect.
Responsibilities
Ensure safety compliance through audits and training.
Lead and motivate a team of assemblers, including training and coaching to leaders and assemblers to improve performance.
Own KPIs such as Safety, FPY, Continuous Improvement, etc.
Write SOPs and implement self-inspection procedures.
Identify process improvements and collaborate with management to enhance productivity, reduce waste, and prevent human errors.
Analyze problems, identify root causes, and implement corrective actions promptly.
Prioritize tasks, manage time, and meet deadlines.
Optimize workflow and lead staff training, fostering a positive work environment.
Maintain training and rework records including quality issues.
Conduct performance evaluations and provide constructive feedback.
Maintain good discipline and housekeeping on the line.
Requirements & Qualifications
Minimum degree in Engineering, Manufacturing or a related field preferred; relevant work experience may be considered in lieu of a degree.
3–5 years of experience in a Manufacturing Engineer role, preferably in a manufacturing environment.
Strong engineering background with excellent problem-solving abilities and a proactive approach to challenges.
Six Sigma Green Belt or higher.
Highly motivated, able to work independently and in a team, with good organizational and communication skills (oral and written).
Familiarity with production management software (ERP & MES) and Root Cause Analysis methodologies.
Excellent communication and interpersonal skills, both written and verbal.
If you have a passion for driving meaningful operational improvements, excel at analytical problem-solving, and thrive in a dynamic scaleup atmosphere, we invite you to join LionsBot and help shape the future of robotics innovation.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Management and Manufacturing
Industries
Automation Machinery Manufacturing
Referrals increase your chances of interviewing at LionsBot International.
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Manufacturing Shift Lead - Biotechnologist
Posted today
Job Viewed
Job Description
About the role
Primary responsibilities include performing routine and critical manufacturing operations with minimal supervision, supporting engineering and validation activities, acting as a deputy to the Shift Supervisor, and delivering excellence in manufacturing processing. The individual will integrate best practices into manufacturing wherever appropriate.
How you will contribute
Primary Responsibility
Execution of all routine and critical operations in both Upstream and Downstream or both Equipment Prep and Buffer Prep areas. Perform commissioning and validation activities in respective areas.
Active participation in troubleshooting. Collaborate with Shift Supervisor, SME and Manufacturing Leadership for issue resolution.
Serve as deputy for Shift Supervisor and acting Supervisor during Supervisor absences.
Monitor material consumption and coordinate all material deliveries.
Learn and perform well‐defined SOPs in all areas of responsibility.
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.
Review manufacturing documentation and EBM or PCS alerts real‐time to ensure compliance if applicable.
Attain operating knowledge of the Process Control System (PCS).
Record data into logbooks and log‐sheets.
Review logbooks and log‐sheets data.
Ensure documentation is complete, reviewed and meets good documentation practices (forms, logbooks, EBM, batch records, etc.).
Perform equipment monitoring.
Perform and coordinate basic laboratory tasks including but not limited to sampling, pH and conductivity measurements.
Demonstrate aseptic technique in the handling of product and materials.
Informing management of events impacting production schedule.
Propose and review document revisions.
Recommend/Implement process changes/improvements or safety/ergonomic improvements.
Complete required training on time.
Carry out work in a safe manner, notifying management of safety issues and risks.
Quality
Lead and participate in investigations of production events in the Global Event Management System (GEMS) or equivalent systems and work with cross‐functional departments to identify root causes.
Complete action items for event investigations.
Implement appropriate CAPAs from event investigations.
Review document revisions of Standard Operating Procedures/Batch Records.
Communicate any quality issues/concerns to Supervisor and QA.
Implement Change Controls for production.
Staff Technical Training and Development
Meet and maintain training requirements.
Develop and maintain personal development plan.
Provide annual performance self‐assessment on development plan.
General Responsibilities
Act as a role model (Lead by Example).
Act as a Subject Matter Expert SME for improvement projects.
Act as a resource / SME for staff.
Provide technical training for area personnel and assess training effectiveness.
Develop training material for technical training.
Assess staff skill sets and provide feedback to Supervisor.
Perform scheduled cleaning of equipment.
Assist in the assembly and disassembly of process equipment.
Perform standardization of equipment.
Perform basic 5S housekeeping.
Corrective Work Orders
Initiate and follow up on Corrective Work Orders in the C3ME system or equivalent system.
Support change over activities.
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 possesses more than 4 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 more than 6 years of relevant experience in the biotechnology or pharmaceutical industry.
Nitec in Biotechnology / Chemical Process Technology or related with more than 8 years of relevant experience in the biotechnology, pharmaceutical industry.
Excellent self‐motivated team player with hands‐on attitude and good communication skills.
Able to work on 12 hours rotating shift.
Will work holidays and overtime as required.
May be required to adjust work schedule to meet production demands.
Key Skills and Competencies
Will be required to perform as a subject matter expert for equipment and/or systems.
Knowledge of cGMP’s and applicable agency regulations (such as the FDA, EMEA) to ensure inspection readiness of department.
Proficient at following written instructions in the form of Electronic Batch Management (EBM), Batch Records (MBRs, MFRs) and Standard Operating Procedures (SOPs) where applicable.
Self‐motivated individual with the ability to complete and manage multiple floor activities in an effective and compliant manner. In the absence of the supervisor, they are the person of authority.
Expected to act on behalf of the supervisor while on the floor.
Demonstrates appropriate level of adaptability, maintains positive outlook, and demonstrates composure under pressure.
Possess excellent communication skills to all levels throughout the organization.
Possess excellent troubleshooting skills.
Proficient documentation and proficient computer skills.
Proficient in aseptic technique where applicable.
Proficient as a system user of business systems such as C3ME and Trackwise.
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).
More about us
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. 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, 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.
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Manufacturing Shift Lead - Biotechnologist
Posted 13 days ago
Job Viewed
Job Description
About the role:
This position is required perform with minimal 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. Will support or lead engineering and validation activities. Deputy to the Shift Supervisor, acting on Supervisor’s behalf when needed. The individual will deliver excellence in manufacturing processing and provide support in integrate best practices, where appropriate, into manufacturing.
How you will contribute:
Primary Responsibility
- Execution of all routine and critical operations in both Upstream and Downstream or both Equipment Prep and Buffer Prep areas. Perform commissioning and validation activities in respective areas.
- Active participation in troubleshooting. Collaborate with Shift Supervisor, SME and Manufacturing Leadership for issue resolution.
- Serve as deputy for Shift Supervisor and acting Supervisor during Supervisor absences
- Monitor material consumption and coordinate all materials deliveries
- Learn and perform well-defined SOPs in all areas of responsibility
- 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
- Review manufacturing documentation and EBM or PCS alerts real-time to ensure compliance if applicable
- Attain operating knowledge of the Process Control System (PCS)
- Record data into logbooks and log-sheets
- Review logbooks and log-sheets data
- Ensure documentation is complete, reviewed and meets good documentation practices (forms, logbooks, EBM, batch records, etc.)
- Perform equipment monitoring
- Perform and coordinate basic laboratory tasks including but not limited to sampling, pH and conductivity measurements
- Demonstrate aseptic technique in the handling of product and materials
- Informing management of events impacting production schedule
- Propose and review document revisions
- Recommend/Implement process changes/improvements or safety/ergonomic improvements.
- Complete required training on time
- Carry out work in a safe manner, notifying management of safety issues and risks
Quality
- Lead and participate in investigations of production events in the Global Event Management System (GEMS) or equivalent systems and work with cross-functional departments to identify root causes.
- Complete action items for event investigations
- Implement appropriate CAPAs from event investigations
- Review document revisions of Standard Operating Procedures/Batch Records
- Communicate any quality issues/concerns to Supervisor and QA
- Implement Change Controls for production
Staff Technical Training and Development
- Meet and maintain training requirements
- Develop and maintain personal development plan
- Provide annual performance self-assessment on development plan
General Responsibilities:
- Act as a role model (Lead by Example)
- Act as a Subject Matter Expert SME for improvement projects
- Act as a resource / SME for staff
- Provide technical training for area personnel and assess training effectiveness
- Develop training material for technical training
- Assess staff skill sets and provide feedback to Supervisor
- Perform scheduled cleaning of equipment
- Assist in the assembly and disassembly of process equipment
- Perform standardization of equipment
- Perform basic 5S housekeeping
Initiate and follow up on Corrective Work Orders in the C3ME system or equivalent system
- Support change over activities
- 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 possesses more than 4 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 more than 6 years of relevant experience in the biotechnology or pharmaceutical industry
- Nitec in Biotechnology / Chemical Process Technology or related with more than 8 years of relevant experience in the biotechnology, pharmaceutical industry.
- Excellent self-motivated team player with hands-on attitude and good communication skills
- Able to work on 12 hours rotating shift
- Will work holidays and overtime as required
- May be required to adjust work schedule to meet production demands
Key Skills and Competencies
- Will be required to perform as a subject matter expert for equipment and/or systems
- Knowledge of cGMP’s and applicable agency regulations (such as the FDA, EMEA) to ensure inspection readiness of department.
- Proficient at following written instructions in the form of Electronic Batch Management (EBM), Batch Records (MBRs, MFRs) and Standard Operating Procedures (SOPs) where applicable
- Self-motivated individual with the ability to complete and manage multiple floor activities in an effective and compliant manner. In the absence of the supervisor, they are the person of authority.
- Expected to act on behalf of the supervisor while on the floor
- Demonstrates appropriate level of adaptability, maintains positive outlook, and demonstrates composure under pressure.
- Possess excellent communication skills to all levels throughout the organization
- Possess excellent troubleshooting skills
- Proficient documentation and proficient computer skills
- Proficient in aseptic technique where applicable
- Proficient as a system user of business systems such as C3ME and Trackwise
- 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)
More about us:
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. 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, 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.
Manufacturing Team Lead - Listed SEMICON
Posted today
Job Viewed
Job Description
Responsibilities:
Lead and supervise a team of manufacturing operators to ensure smooth and efficient production operations.
Monitor production schedules and targets, and take corrective actions as needed to meet customer requirements.
Train new employees on safety procedures, equipment operation, and manufacturing processes.
Develop and implement standard operating procedures (SOPs) to ensure consistent quality and productivity.
Coordinate with other departments to ensure timely availability of materials and resources for production.
Perform regular inspections to ensure adherence to quality standards and identify areas for improvement.
Effectively communicate with team members, management, and cross-functional teams to address any issues and drive continuous improvement.
Ensure compliance with company policies, safety regulations, and industry standards.
Diploma or Degree in Engineering or related field.
With 2 years of experience in the wafer fab/ semiconductor industry.
Prior experience in a leadership or team lead role.
Ability to lead and motivate a team in a fast-paced environment.
If you are interested in the advertised position, please click on the
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EA License No: 13C6305
Reg. No.: R
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Lead Manufacturing Manager
Posted today
Job Viewed
Job Description
The Lead Manufacturing Manager will be responsible for overseeing the daily activities of a manufacturing team.
Key Responsibilities- Communicate job expectations to the team and ensure they meet their objectives.
- Maintain accurate records of production planning, monitoring, and appraisal.
- Provide coaching, counseling, and discipline as needed to employees.
- Develop and implement procedures to improve productivity.
- Facilitate open communication among team members and resolve conflicts.
We appreciate your interest in this position. Only shortlisted candidates will be contacted.
· M-Power Human Resource Pte.Ltd.
· EA License No: 16C8377
· EAP Name/ Registered No: Liu Zhe / R