259 Biotechnologist jobs in Singapore

Biotechnologist

$60000 - $120000 Y GSK

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Job Description

Site Name:
Singapore - Tuas

Posted Date:
Jan

As a Biotechnologist in our Value Stream, you will participate in the preparation, operation and completion of assigned process stages to ensure the production of bulk drug substances is within establish timing and quality standards. You will also ensure good housekeeping of the facilities to keep them in good operational order in line with cGMP, safety and environmental requirements.

* Key Responsibilities:*
Operations

  • Adhere to cGMP and safety requirements
  • Ensure good housekeeping of associated production facilities so that they are kept in good operational order
  • Identify areas for improvement and participate in continuous improvement projects to enhance operational effectiveness and efficiency
  • Participate in commissioning and qualification activities as required
  • Carry out other related duties as assigned by the N+1
  • Assigned as in-charge by process/operations area to provide guidance/leadership to ensure processes are completed reliably

Planning

  • Follow the day-to-day planning
  • Assist Lead Biotechnologist or Shift Supervisor or Operations Superintendent in detailed team operations planning

Training & Development

  • Ensure that he/she is trained/qualified in the current effective SOP and OJT in accordance with the assigned training curricula prior to commencing operation.
  • Proactively engage N+1 to discuss personal development and follow up on agreed development plan.
  • To provide guidance and support to new joiner ensuring his/her smooth transition to the new environment
  • To develop oneself as a process SME
  • Guide junior employees to ensure knowledge transfer for business continuity.
  • Conduct classroom and on-the-job (OJT) training as assigned.

Quality

  • Comply with all relevant SOP/Batch record requirements.
  • Perform timely review of documentation and make necessary corrections.
  • Have good quality mindset and integrity to ensure products are manufactured with the highest quality
  • Participate in deviation investigation process (Process, Environmental, Maintenance/Equipment, QC) and implementation of Corrective and Preventive Action (CAPA)
  • Participate in cGMP self-inspections to ensure compliance with internal SOPs and regulatory requirements

Reporting/Documentation

  • Operate key computer applications related to production function
  • Ensure that batch record, checklist and logbooks are correctly recorded, cGMP complied and maintained
  • Maintain clear communication with N+1 and fellow colleagues, providing clear feedback of any items pertaining to safety, quality and efficiency
  • Participation in development and generation of production checklist, SOPs, validation protocols and the regular review and updates of these documents
  • Perform VS review of completed documentation to ensure adherence to GDP
  • To lead design/drafting of working instruction to ensure that it is user friendly to improve GDP

Technology Transfer

  • Participate in new technology and/or new process transfer

Security/Safety/Environment

  • Awareness and adherence to site safety procedure.
  • Ensure safe operations on the field
  • Identify and report all potential safety issues (personal protection requirement, equipment protection, way of working etc).
  • Ensure proper housekeeping of assigned production areas to minimize safety hazards
  • Participate in Safety Inspections
  • Participate in Workplace Risk Assessment

Interface with other Department/Team

  • Coordination with department colleagues to ensure

  • Timely supplies of materials and buffers

  • Calibration/maintenance activities are supported.
  • Open communication on sampling requirements to QC department
  • Establish good working relationship with QA, QC, maintenance, calibration to ensure smooth operations.

Basic Qualifications

  • NITEC/Diploma in chemical technology, chemical engineering or biotechnology engineering
  • Min 2 years of experience in Biologics, Chemical or Pharmaceutical industry
  • Experience in working with GMP
  • Familiar with purification/fermentation/conjugation/isolator operations/material and buffer operations

If you have the following characteristics, it would be a plus:

  • A good team player and able to work independently
  • Good communication and documentation skills
  • Has disciplined and quality mindset
  • Comfortable to work in a cleanroom environment.

To learn more about Singapore GSK and our people, please click on this link:

Why GSK?
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

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Biotechnologist

$90000 - $120000 Y BNF Group

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Job Description

BNF is looking for a versatile and hands-on Biotechnologist to join our team and focus on developing and scaling up fermentation technologies. This role is ideal for someone who enjoys problem-solving across disciplines and is excited to work at the interface of lab-scale R&D and real-world deployment.

You'll run fermentation experiments, operate pilot systems, and support the scale-up of bioprocesses, while also contributing to adjacent R&D and process innovation projects as the company evolves.

Key Responsibilities: Fermentation & Process DevelopmentDesign, set up, and run bench- and pilot-scale fermentation systems under both aerobic and anaerobic conditionsOptimise microbial growth and conversion parameters (e.g., pH, temperature, retention time, gas flow, agitation)Record, analyse, and present experimental data to guide system improvements and scaling strategies

Scale-Up & Prototyping Translate lab findings into scalable process concepts, equipment sizing, and process flow diagrams (PFDs)Support design, fabrication, anpd testing of pilot and pre-commercial systems, working closely with external partners and vendorsTroubleshoot and iterate prototypes based on performance data, integrating both engineering and biological insights

Cross-Functional R&D Collaborate with operations teams on multi-disciplinary projectsAssist with adjacent R&D efforts (e.g., pre-treatment, recovery processes, digital monitoring systems) as neededContribute to rapid prototyping, new concept evaluation, and internal process improvement initiativesSupport other R&D initiatives as required

Field Testing & Deployment Support commissioning, monitoring, and optimisation of deployed systems in pilot or customer environmentsParticipate in field trials, technology demonstrations, and documentation for knowledge transfer

What We're Looking For: Bachelor's or Master's, or PhD degree in Chemistry, Biochemistry, Food Science, Chemical Engineering, Bioprocess Engineering, Environmental Engineering, or a related field2–6 years of experience in fermentation process development, pilot systems, or engineering R&D (startup or tech development experience a plus)Familiarity with fermentation principles, bioreactor operation, and biological process troubleshootingComfort working on evolving systems, rapidly adapting to changes, and iterating based on real-world resultsExperience building, operating, or scaling pilot setups or experimental rigsSolid documentation habits, strong communication skills, and a collaborative mindset

Bonus Points (Nice to Have): Experience with downstream processing (filtration, separation, etc.)CAD or process design tools (e.g., AutoCAD, SolidWorks, P&ID software)Exposure to hardware prototyping, control systems, or process automationInterest in sustainability, circular economy, or bio-based innovation

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Biotechnologist

Singapore, Singapore $40000 - $60000 Y INTEGRIX SOLUTIONS PTE. LTD.

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Job Description

About the Role:

We invite highly motivated graduates to join our team in providing support to our clients' biomanufacturing facilities. In this entry-level role, you will assist with routine manufacturing activities, process monitoring, and quality checks to ensure smooth operation of our clients' biotech production processes. Working under guidance, you will gain hands-on exposure to GMP practices, bioprocess equipment, and documentation standards

Key Responsibilities:

  • Assist in preparation of culture media, buffers, and solutions for production processes.
  • Operate and monitor bioprocess equipment such as bioreactors, fermenters, filtration systems, and chromatography units under supervision.
  • Support scale-up and production runs while following established SOPs and batch records.
  • Perform in-process quality checks and record production parameters accurately.
  • Ensure proper cleaning, sterilization, and maintenance of production areas and equipment.
  • Follow all safety, environmental, and regulatory guidelines in compliance with GMP standards.
  • Assist in troubleshooting basic process deviations and support process improvement initiatives.
  • Collaborate with quality assurance, R&D, and engineering teams to ensure smooth production workflows.

Requirements:

  • Diploma in a Science or Engineering related field, such as Biotechnology, Bioprocess Engineering, Biochemistry, Microbiology, Chemical Engineering.
  • Fundamental understanding of bioprocessing techniques such as fermentation, cell culture, or downstream processing.
  • Knowledge of laboratory safety, aseptic techniques, and basic instrumentation.
  • Strong attention to detail with excellent organisational and documentation skills.
  • Ability to work in shifts and adapt to a regulated production environment.
  • Eagerness to learn, contribute, and grow in an industrial biotechnology setting.
  • Internship, academic project, or industrial training related to bioprocessing or production will have an added advantage.

What We Offer:

  • Opportunity to work in Singapore's thriving biomanufacturing industry
  • Structured on-the-job training in modern industrial-scale bioprocessing facilities.
  • Career growth pathway within production and process development teams.
  • Collaborative and supportive team environment.
  • One-year contract, renewable upon completion.
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Biotechnologist

Singapore, Singapore $90000 - $120000 Y BNL WASTE MANAGEMENT PTE. LTD.

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Job Viewed

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Job Description

BNF is looking for a versatile and hands-on Biotechnology Engineer to join our team and focus on developing and scaling up fermentation technologies . This role is ideal for someone who enjoys problem-solving across disciplines and is excited to work at the interface of lab-scale R&D and real-world deployment .

You'll run fermentation experiments, operate pilot systems, and support the scale-up of bioprocesses, while also contributing to adjacent R&D and process innovation projects as the company evolves.

Key Responsibilities:

Fermentation & Process Development

  • Design, set up, and run bench- and pilot-scale fermentation systems under both aerobic and anaerobic conditions
  • Optimise microbial growth and conversion parameters (e.g., pH, temperature, retention time, gas flow, agitation)
  • Record, analyse, and present experimental data to guide system improvements and scaling strategies

Scale-Up & Prototyping

  • Translate lab findings into scalable process concepts, equipment sizing, and process flow diagrams (PFDs)
  • Support design, fabrication, anpd testing of pilot and pre-commercial systems, working closely with external partners and vendors
  • Troubleshoot and iterate prototypes based on performance data, integrating both engineering and biological insights

Cross-Functional R&D

  • Collaborate with operations teams on multi-disciplinary projects
  • Assist with adjacent R&D efforts (e.g., pre-treatment, recovery processes, digital monitoring systems) as needed
  • Contribute to rapid prototyping, new concept evaluation, and internal process improvement initiatives
  • Support other R&D initiatives as required

Field Testing & Deployment

  • Support commissioning, monitoring, and optimisation of deployed systems in pilot or customer environments
  • Participate in field trials, technology demonstrations, and documentation for knowledge transfer

What We're Looking For:

  • Bachelor's or Master's degree in Chemistry, Biochemistry, Food Science, Chemical Engineering, Bioprocess Engineering, Environmental Engineering, or a related field
  • 2–6 years of experience in fermentation process development, pilot systems, or engineering R&D (startup or tech development experience a plus)
  • Familiarity with fermentation principles, bioreactor operation, and biological process troubleshooting
  • Comfort working on evolving systems, rapidly adapting to changes, and iterating based on real-world results
  • Experience building, operating, or scaling pilot setups or experimental rigs
  • Solid documentation habits, strong communication skills, and a collaborative mindset

Bonus Points (Nice to Have):

  • Experience with downstream processing (filtration, separation, etc.)
  • CAD or process design tools (e.g., AutoCAD, SolidWorks, P&ID software)
  • Exposure to hardware prototyping, control systems, or process automation
  • Interest in sustainability, circular economy, or bio-based innovation
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Biotechnologist

Singapore, Singapore GlaxoSmithKline

Posted today

Job Viewed

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Job Description

Location: Singapore – Tuas. Posted: Jan .
As a Biotechnologist in our Value Stream, you will participate in the preparation, operation and completion of assigned process stages to ensure the production of bulk drug substances is within established timing and quality standards. You will also ensure good housekeeping of the facilities to keep them in good operational order in line with cGMP, safety and environmental requirements.
Key Responsibilities
Adhere to cGMP and safety requirements.
Ensure good housekeeping of associated production facilities so that they are kept in good operational order.
Identify areas for improvement and participate in continuous improvement projects to enhance operational effectiveness and efficiency.
Participate in commissioning and qualification activities as required.
Carry out other related duties as assigned by the N+1.
Assigned as in-charge by process/operations area to provide guidance/leadership to ensure processes are completed reliably.
Operations
Adhere to cGMP and safety requirements.
Ensure good housekeeping of associated production facilities so that they are kept in good operational order.
Identify areas for improvement and participate in continuous improvement projects to enhance operational effectiveness and efficiency.
Participate in commissioning and qualification activities as required.
Carry out other related duties as assigned by the N+1.
Assigned as in-charge by process/operations area to provide guidance/leadership to ensure processes are completed reliably.
Planning
Follow the day‐to‐day planning.
Assist Lead Biotechnologist or Shift Supervisor or Operations Superintendent in detailed team operations planning.
Training & Development
Ensure that he/she is trained/qualified in the current effective SOP and OJT in accordance with the assigned training curricula prior to commencing operation.
Proactively engage N+1 to discuss personal development and follow up on agreed development plan.
To provide guidance and support to new joiner ensuring his/her smooth transition to the new environment.
To develop oneself as a process SME.
Guide junior employees to ensure knowledge transfer for business continuity.
Conduct classroom and on‐the‐job (OJT) training as assigned.
Quality
Comply with all relevant SOP/Batch record requirements.
Perform timely review of documentation and make necessary corrections.
Have good quality mindset and integrity to ensure products are manufactured with the highest quality.
Participate in deviation investigation process (Process, Environmental, Maintenance/Equipment, QC) and implementation of Corrective and Preventive Action (CAPA).
Participate in cGMP self‐inspections to ensure compliance with internal SOPs and regulatory requirements.
Reporting/Documentation
Operate key computer applications related to production function.
Ensure that batch record, checklist and logbooks are correctly recorded, cGMP complied and maintained.
Maintain clear communication with N+1 and fellow colleagues, providing clear feedback of any items pertaining to safety, quality and efficiency.
Participation in development and generation of production checklist, SOPs, validation protocols and the regular review and updates of these documents.
Perform VS review of completed documentation to ensure adherence to GDP.
To lead design/drafting of working instruction to ensure that it is user friendly to improve GDP.
Technology Transfer
Participate in new technology and/or new process transfer.
Security/Safety/Environment
Awareness and adherence to site safety procedure.
Ensure safe operations on the field.
Identify and report all potential safety issues (personal protection requirement, equipment protection, way of working etc.).
Ensure proper housekeeping of assigned production areas to minimize safety hazards.
Participate in Safety Inspections.
Participate in Workplace Risk Assessment.
Interface with other Department/Team
Coordination with department colleagues to ensure timely supplies of materials and buffers.
Calibration/maintenance activities are supported.
Open communication on sampling requirements to QC department.
Establish good working relationship with QA, QC, maintenance, calibration to ensure smooth operations.
Basic Qualifications
NITEC/Diploma in chemical technology, chemical engineering or biotechnology engineering.
Min 2 years of experience in Biologics, Chemical or Pharmaceutical industry.
Experience in working with GMP.
Familiar with purification/fermentation/conjugation/isolator operations/material and buffer operations.
Plus Characteristics
A good team player and able to work independently.
Good communication and documentation skills.
Has disciplined and quality mindset.
Comfortable to work in a cleanroom environment.
#J-18808-Ljbffr

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Biotechnologist

Singapore, Singapore ANTAES ASIA PTE. LTD.

Posted today

Job Viewed

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Job Description

Job Description:
Contribute to Life Science projects for Antaes Asia clients
Configure and troubleshoot DeltaV batch recipes, including parameter inputs and sequencing logic.
Review batch data and trends to ensure process consistency and quality.
Support the implementation and testing of DCS logic, including interlocks, handshakes, and system prompts across unit operations.
Collaborate with Automation and Engineering teams to enhance recipe performance and control strategies.
Provide technical support for operations involving centrifugation and/or ultrafiltration (UF) systems.
Participate in equipment readiness, startup, and batch execution support.
Ensure compliance with SOPs, batch records, and GMP requirements.
Prepare and review technical documents including process instructions, automation specs, and troubleshooting guides.
Work closely with cross-functional teams including MSAT, QA, Engineering, and Manufacturing to ensure seamless execution of production activities.
Contribute to the promotion of Antaes services on top of assistance provided to clients
Job Requirements:
Bachelor degree in Science, Chemical Engineering, Mechanical Engineering, Manufacturing Engineering, Biotechnology, or related Life Science
5 – 8 years’ experience in biotechnologist or process engineering roles
Strong hands-on experience with DeltaV automation systems.
Proficient in designing, modifying, or troubleshooting batch recipes and DCS logic (e.g., handshakes, prompts).
Familiarity with centrifuge and/or ultrafiltration (UF) operations.
Understanding of biopharmaceutical manufacturing and cleanroom practices.
Adherence to safety protocols and global regulatory compliance
Candidate must be highly motivated, be able to work independently as well as in a team and have good organizational and oral and written communication skills
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Biotechnologist

486781 $6500 Monthly BNL WASTE MANAGEMENT PTE. LTD.

Posted 5 days ago

Job Viewed

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Job Description

Job Description & Requirements


BNL is looking for a versatile and hands-on Biotechnology Engineer to join our team and focus on developing and scaling up fermentation technologies . This role is ideal for someone who enjoys problem-solving across disciplines and is excited to work at the interface of lab-scale R&D and real-world deployment .


You’ll run fermentation experiments, operate pilot systems, and support the scale-up of bioprocesses, while also contributing to adjacent R&D and process innovation projects as the company evolves.


Key Responsibilities:

Fermentation & Process Development

  • Design, set up, and run bench- and pilot-scale fermentation systems under both aerobic and anaerobic conditions
  • Optimise microbial growth and conversion parameters (e.g., pH, temperature, retention time, gas flow, agitation)
  • Record, analyse, and present experimental data to guide system improvements and scaling strategies

Scale-Up & Prototyping

  • Translate lab findings into scalable process concepts, equipment sizing, and process flow diagrams (PFDs)
  • Support design, fabrication, anpd testing of pilot and pre-commercial systems, working closely with external partners and vendors
  • Troubleshoot and iterate prototypes based on performance data, integrating both engineering and biological insights

Cross-Functional R&D

  • Collaborate with operations teams on multi-disciplinary projects
  • Assist with adjacent R&D efforts (e.g., pre-treatment, recovery processes, digital monitoring systems) as needed
  • Contribute to rapid prototyping, new concept evaluation, and internal process improvement initiatives
  • Support other R&D initiatives as required

Field Testing & Deployment

  • Support commissioning, monitoring, and optimisation of deployed systems in pilot or customer environments
  • Participate in field trials, technology demonstrations, and documentation for knowledge transfer

What We’re Looking For:

  • Bachelor’s or Master’s degree in Chemistry, Biochemistry, Food Science, Chemical Engineering, Bioprocess Engineering, Environmental Engineering, or a related field
  • 2–6 years of experience in fermentation process development, pilot systems, or engineering R&D (startup or tech development experience a plus)
  • Familiarity with fermentation principles, bioreactor operation, and biological process troubleshooting
  • Comfort working on evolving systems, rapidly adapting to changes, and iterating based on real-world results
  • Experience building, operating, or scaling pilot setups or experimental rigs
  • Solid documentation habits, strong communication skills, and a collaborative mindset

Bonus Points (Nice to Have):

  • Experience with downstream processing (filtration, separation, etc.)
  • CAD or process design tools (e.g., AutoCAD, SolidWorks, P&ID software)
  • Exposure to hardware prototyping, control systems, or process automation
  • Interest in sustainability, circular economy, or bio-based innovation
This advertiser has chosen not to accept applicants from your region.
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Biotechnologist

018989 $7000 Monthly ANTAES ASIA PTE. LTD.

Posted 12 days ago

Job Viewed

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Job Description

Job Description:

  • Contribute to Life Science projects for Antaes Asia clients
  • Configure and troubleshoot DeltaV batch recipes, including parameter inputs and sequencing logic.
  • Review batch data and trends to ensure process consistency and quality.
  • Support the implementation and testing of DCS logic, including interlocks, handshakes, and system prompts across unit operations.
  • Collaborate with Automation and Engineering teams to enhance recipe performance and control strategies.
  • Provide technical support for operations involving centrifugation and/or ultrafiltration (UF) systems.
  • Participate in equipment readiness, startup, and batch execution support.
  • Ensure compliance with SOPs, batch records, and GMP requirements.
  • Prepare and review technical documents including process instructions, automation specs, and troubleshooting guides.
  • Work closely with cross-functional teams including MSAT, QA, Engineering, and Manufacturing to ensure seamless execution of production activities.
  • Contribute to the promotion of Antaes services on top of assistance provided to clients

Job Requirements:

  • Bachelor degree in Science, Chemical Engineering, Mechanical Engineering, Manufacturing Engineering, Biotechnology, or related Life Science
  • 5 – 8 years’ experience in biotechnologist or process engineering roles
  • Strong hands-on experience with DeltaV automation systems.
  • Proficient in designing, modifying, or troubleshooting batch recipes and DCS logic (e.g., handshakes, prompts).
  • Familiarity with centrifuge and/or ultrafiltration (UF) operations.
  • Understanding of biopharmaceutical manufacturing and cleanroom practices.
  • Adherence to safety protocols and global regulatory compliance
  • Candidate must be highly motivated, be able to work independently as well as in a team and have good organizational and oral and written communication skills
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Biotechnologist Intern

Sanofi Group

Posted 3 days ago

Job Viewed

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Job Description

Sanofi Manufacturing and Supply (M&S) Organization is preparing its future through an ambitious program named Modulus Facility. The facility is at the cornerstone of Sanofi strategy as it aims at creating a new manufacturing concept consisting of a new generation of evolutive multi-product facilities, modular, adaptable, and agile, leveraging new disruptive technologies, to better address the supply of Vaccine and Specialty Care Biologics products. One of these two Modulus Facilities is constructed in Singapore at a new Greenfield site, with a design similar to the one in Neuville (France). The facilities will also have highly digitalized and automated capabilities which is a key enabler for operations using technologies such as autonomous guided vehicles, cobots and cloud systems.
We are seeking motivated and enthusiastic individuals for the role of **Biotechnologist Intern, Manufacturing** . As a member of our **manufacturing operations team** , you will be directly involved in running the manufacturing operations in a state-of-the-art biomanufacturing facility.
This is a hands-on opportunity to contribute to core GMP operations while developing valuable technical and operational experience in biologics manufacturing. The candidate will have a routine operational role consisting of the following:
+ Execute **routine GMP manufacturing operations** in compliance with established Process, Quality, and Safety standards.
+ Maintain **cleanliness and organization** of manufacturing areas via standard housekeeping procedures.
+ Assist in **regulatory readiness activities** , including documentation and audit support.
+ Use key **digital tools and automation platforms** to perform manufacturing tasks and record operations.
+ Participate in **continuous improvement initiatives** to optimize processes and increase operational efficiency.
Sanofi MODULUS Singapore is hiring for Intern _Biotechnologist Intern, Manufacturing_ for the following teams:
+ Upstream Manufacturing Process
+ Downstream Manufacturing Process
+ Central Manufacturing Services (Media & Buffer, Logistics)
**Work Environment**
+ This role is based at our Modulus facility in Tuas, Singapore, requiring full-time presence on-site.
+ The nature of manufacturing operations requires the need for presence on the floor to support and perform manufacturing operations.
+ While we prioritize on-site work to maximize collaboration, we understand the need for flexibility. Ad hoc work-from-home arrangements can be discussed and may be approved based on individual circumstances and business needs.
The successful applicant will be part of a **12-hour rotating shift pattern** , which includes **day and night shifts** , including **weekends** . Shift allowance and company transport is provided at dedicated MRT stations to enable you to commute to and from work safely for staff working on shift.
**Performance Standards: Duties & Responsibilities**
**Key Areas**
**Action Areas, Deliverables and Outcomes**
**Weightage**
**(Total 100%)**
Commissioning and Qualification Activities, Operational Readiness and Continuous Improvement projects - 10%
+ Perform and execute commissioning activities for manufacturing equipment and systems.
+ Support the documentation readiness for procedures, risk assessment and other training documents for the manufacturing equipment and systems.
+ Support continuous improvement initiatives related to routine operations
cGMP Manufacturing Operations - 90%
+ Perform and participate in the routine Product Runs in the Modulus Facility
**Pre-requisites**
**Knowledge, Skills & Competencies / Language**
+ Self-starter with the ability to work independently while contributing effectively within cross-functional teams.
+ Thrives in fast-paced, dynamic environments and is comfortable working under tight deadlines.
+ Excellent verbal communication and presentation skills, with the ability to tailor messages appropriately for different audiences and stakeholders.
+ Proficient in technical writing, with a clear and structured approach to documenting processes and findings.
+ A reliable and collaborative team player who values collective success and mutual support.
**Qualifications / Requirement**
+ Currently pursuing or recently completed a **Degree in Biotechnology, Life Sciences, Chemical, Pharmaceutical Engineering** , or a related field.
+ Strong interest in biologics manufacturing and GMP operations.
+ Willingness to work on site and 12-hour shifts.
+ Good understanding of laboratory safety and basic biotech processes.
+ Ability to work in a team-oriented, fast-paced environment.
+ Familiarity with digital manufacturing systems (e.g., MES, ERP) is a plus.
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (
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Biotechnologist Intern

Sanofi Group

Posted 3 days ago

Job Viewed

Tap Again To Close

Job Description

Sanofi Manufacturing and Supply (M&S) Organization is preparing its future through an ambitious program named Modulus Facility. The facility is at the cornerstone of Sanofi strategy as it aims at creating a new manufacturing concept consisting of a new generation of evolutive multi-product facilities, modular, adaptable, and agile, leveraging new disruptive technologies, to better address the supply of Vaccine and Specialty Care Biologics products. One of these two Modulus Facilities is constructed in Singapore at a new Greenfield site, with a design similar to the one in Neuville (France). The facilities will also have highly digitalized and automated capabilities which is a key enabler for operations using technologies such as autonomous guided vehicles, cobots and cloud systems.
We are seeking motivated and enthusiastic individuals for the role of **Biotechnologist Intern, Manufacturing** . As a member of our **manufacturing operations team** , you will be directly involved in running the manufacturing operations in a state-of-the-art biomanufacturing facility.
This is a hands-on opportunity to contribute to core GMP operations while developing valuable technical and operational experience in biologics manufacturing. The candidate will have a routine operational role consisting of the following:
+ Execute **routine GMP manufacturing operations** in compliance with established Process, Quality, and Safety standards.
+ Maintain **cleanliness and organization** of manufacturing areas via standard housekeeping procedures.
+ Assist in **regulatory readiness activities** , including documentation and audit support.
+ Use key **digital tools and automation platforms** to perform manufacturing tasks and record operations.
+ Participate in **continuous improvement initiatives** to optimize processes and increase operational efficiency.
Sanofi MODULUS Singapore is hiring for Intern _Biotechnologist Intern, Manufacturing_ for the following teams:
+ Upstream Manufacturing Process
+ Downstream Manufacturing Process
+ Central Manufacturing Services (Media & Buffer, Logistics)
**Work Environment**
+ This role is based at our Modulus facility in Tuas, Singapore, requiring full-time presence on-site.
+ The nature of manufacturing operations requires the need for presence on the floor to support and perform manufacturing operations.
+ While we prioritize on-site work to maximize collaboration, we understand the need for flexibility. Ad hoc work-from-home arrangements can be discussed and may be approved based on individual circumstances and business needs.
The successful applicant will be part of a **12-hour rotating shift pattern** , which includes **day and night shifts** , including **weekends** . Shift allowance and company transport is provided at dedicated MRT stations to enable you to commute to and from work safely for staff working on shift.
**Performance Standards: Duties & Responsibilities**
**Key Areas**
**Action Areas, Deliverables and Outcomes**
**Weightage**
**(Total 100%)**
Commissioning and Qualification Activities, Operational Readiness and Continuous Improvement projects - 10%
+ Perform and execute commissioning activities for manufacturing equipment and systems.
+ Support the documentation readiness for procedures, risk assessment and other training documents for the manufacturing equipment and systems.
+ Support continuous improvement initiatives related to routine operations
cGMP Manufacturing Operations - 90%
+ Perform and participate in the routine Product Runs in the Modulus Facility
**Pre-requisites**
**Knowledge, Skills & Competencies / Language**
+ Self-starter with the ability to work independently while contributing effectively within cross-functional teams.
+ Thrives in fast-paced, dynamic environments and is comfortable working under tight deadlines.
+ Excellent verbal communication and presentation skills, with the ability to tailor messages appropriately for different audiences and stakeholders.
+ Proficient in technical writing, with a clear and structured approach to documenting processes and findings.
+ A reliable and collaborative team player who values collective success and mutual support.
**Qualifications / Requirement**
+ Currently pursuing or recently completed a **Degree in Biotechnology, Life Sciences, Chemical, Pharmaceutical Engineering** , or a related field.
+ Strong interest in biologics manufacturing and GMP operations.
+ Willingness to work on site and 12-hour shifts.
+ Good understanding of laboratory safety and basic biotech processes.
+ Ability to work in a team-oriented, fast-paced environment.
+ Familiarity with digital manufacturing systems (e.g., MES, ERP) is a plus.
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (
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