265 Biotechnologist jobs in Singapore

Direct message the job poster from Cordlife Singapore

Deputy Group Director - OD & HR | Certified Human Resources Professional | Expert in Multi-Country OD Interventions and Change Management |…

Job Title: Laboratory Biotechnologist

About the Role

Cordlife is seeking a dedicated and skilled Laboratory Biotechnologist to join our dynamic team. This role is directly responsible for the laboratory processing and storage preparation of clients’ umbilical cord blood units and cord tissue, ensuring adherence to the highest standards of quality and compliance.

Key Responsibilities

• Perform processing and storage of umbilical cord blood units and cord tissue.
• Ensure all laboratory activities comply with documented procedures and protocols.
• Generate clinical reports with accuracy and integrity.
• Maintain sterile technique and laboratory safety standards.
• Support the Laboratory Manager with other tasks and responsibilities as assigned.
• Be available for rostered weekend work and occasional out-of-hours duties.

Requirements

Academic Background

• Diploma in Medical Technology or a related discipline.

Experience & Skills

• Experience with sterile techniques.
• Strong sense of responsibility with the ability to work independently as well as in a team.
• Effective verbal and written communication skills.
• Hepatitis B immunization is mandatory.

Personal Attributes

• Self-motivated, reliable, and able to handle tasks without supervision.
• Team-oriented with strong collaboration skills.

Seniority level

• Seniority level Entry level

Employment type

• Employment type Full-time

Job function

• Job function Health Care Provider
• Industries Biotechnology Research and Hospitals and Health Care

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Cordlife is seeking a dedicated and skilled Laboratory Biotechnologist to join our dynamic team. This role is directly responsible for the laboratory processing and storage preparation of clients’ umbilical cord blood units and cord tissue, ensuring adherence to the highest standards of quality and compliance.

Key Responsibilities

• Perform processing and storage of umbilical cord blood units and cord tissue.
• Ensure all laboratory activities comply with documented procedures and protocols.
• Generate clinical reports with accuracy and integrity.
• Maintain sterile technique and laboratory safety standards.
• Support the Laboratory Manager with other tasks and responsibilities as assigned.
• Be available for rostered weekend work and occasional out-of-hours duties.

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Responsibilities:

• Develop and optimize manufacturing processes for biotechnology products, ensuring scalability and efficiency.

• Operate and maintain bioreactors, fermenters, and other specialized equipment used in the manufacturing process.

• Conduct quality control tests and assessments to ensure compliance with regulatory standards and product specifications.

• Collaborate with cross-functional teams, including research and development, to implement process improvements and drive innovation.

• Maintain accurate documentation and records of manufacturing processes, ensuring traceability and adherence to regulatory guidelines.

• Stay updated with industry trends and advancements in manufacturing technologies and implement best practices accordingly.

Scop of the work:

• Perform activities in GXP environment. Activities including but not limited to, manufacturing operations, Commissioning & Qualification activities, any other activities as instructed by the supervisor.

• To perform and execute GXP operations independently and in accordance with Site safety standards

• To support manufacturing activities by performing verification of Automation or MES recipes

• Lead and drive manufacturing improvement initiates

• Perform update of Standard Operating Procedures and Training Procedures

Requirements:

• Min 2 years of working experience required in similar role.

• Experience in the pharmaceutical industry would be an added advantage.

• Strong knowledge of bioprocessing techniques, including fermentation, purification, and downstream processing.

• Proficiency in operating and troubleshooting bioreactors, centrifuges, chromatography systems, and other related equipment.

• Familiarity with quality control procedures and regulatory compliance in the biotechnology sector, particularly in Singapore.

• Excellent problem-solving skills and ability to work independently and in a team-oriented environment.

• Strong organizational and communication skills.

• This is a one-year contract role with continues extension.
  
  
  Please note: This position is not suitable for Lab Technicians, so we kindly ask that lab technicians refrain from applying

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The incumbent will be involved in day-to-day support in biologics and vaccine manufacturing operation by providing operation/maintenance input and facilitate decision making. He/she will act as user representative/area owner in terms of technical transfer of process and product from R&D and CMC to GMP clinical manufacturing of different modalities and platforms to meet tech transfer objectives and timeline. He/she will commission first of its kind multiproduct cGMP manufacturing suites (mammalian, microbial suites) within project timeline and budget.

Job scope

RESPONSIBILITIES:

• Responsible in ensuring that the manufacturing activities are performed in accordance with EHS guidelines and in a cGMP-compliant manner.
• Provide input to operation and equipment in the tech transfer activities of new product/process.
• Draft, author and/or provide inputs in documentations such as facility fit assessment, user requirements, raw material identification, batch records, SOPs, and process recipes.
• To coordinate with relevant departments, stakeholders in tracking of operation progression to ensure project milestones are met.
• Perform and lead root cause analysis for operational related deviations and investigations using established problem-solving tools.
• Train and coach manufacturing team in process and equipment knowledge to ensure operations are conducted in a safe manner.
• Manage change controls and deviations of GMP runs for clinical manufacturing.
• Support process/equipment qualification/validation activities and studies.
• Front auditors during regulatory audits as the SMEs of the department.
• Perform cleaning of equipment and cleanrooms as and when necessary.

EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:

• Bachelor’s degree in a engineering/scientific discipline (Bio/chemical engineering/life science/biology/chemistry) with 2-6 years relevant industry experience.
• Plant start-up or commissioning and/or operational experience in biologics and/or vaccines
• Biological technology transfer experience will be an advantage
• Experience/knowledge of cGMP practices applicable to upstream/downstream virus manufacturing processes, process development is desirable
• Thorough knowledge of Good Documentation Practices (GDP) and Current Good Manufacturing Practices (cGMP)
• Well-organized and detail-oriented, with ability to effectively prioritize tasks with agility, eager to learn, interact and collaborate effectively with various stakeholders in a team environment and consistently demonstrate reliability and responsibility.
• Good team player with good working ethics, initiative, diplomacy, positive influencing abilities and drive.
• Good oral communication and demonstrable, exemplary writing skills.
• Experience with problem solving and statistical tools will be an advantage

Seniority level

• Seniority level Associate

Employment type

• Employment type Full-time

Job function

• Job function Engineering, Research, and Manufacturing
• Industries Research Services and Biotechnology Research

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Join us to apply for the Biotechnologist, Manufacturing role at Sanofi .

Sanofi's Manufacturing and Supply organization is advancing its future through the Modulus program, which aims to create new, modular, and automated multi-product manufacturing facilities leveraging disruptive technologies. One such facility is being built in Singapore on a Greenfield site, mirroring the design in Neuville, France, with highly digitalized capabilities including AGVs, cobots, and cloud systems.

This role, titled Biotechnologist, Manufacturing , reports to the Manager, Manufacturing, and involves working as part of the pioneering shift team in a state-of-the-art facility, participating in engineering and product validation runs.

The routine operational responsibilities include:

• Performing commissioning and qualification activities of equipment and digital systems.
• Executing routine GMP manufacturing activities according to Process, Quality, and Safety standards.
• Maintaining general housekeeping in manufacturing areas.
• Supporting regulatory and audit readiness.
• Utilizing manufacturing digital applications like ERP, MES, PCS.
• Contributing to continuous improvement projects.

Sanofi Modulus Singapore is hiring for teams in:

• Upstream Manufacturing Process
• Downstream Manufacturing Process
• Central Manufacturing Services (Media & Buffer, Logistics)

The main responsibilities include:

• Commissioning and qualification of manufacturing equipment and systems.
• Supporting documentation for procedures, risk assessments, and training.
• Participating in tech transfer and validation runs.

Qualifications:

• Degree in Engineering or Science.
• Relevant internship or industrial experience in biopharmaceuticals is advantageous.
• Self-motivated, independent, and capable of working in cross-functional teams.
• Strong analytical, problem-solving, and communication skills.
• Willingness to work in a rotating shift pattern including weekends.

Join Sanofi to pursue progress and discover the extraordinary in science and healthcare. We are committed to equal opportunity employment.

Details

• Seniority level: Entry level
• Employment type: Full-time
• Job function: Research, Analysis, IT
• Industry: Pharmaceutical Manufacturing

This job posting is active and accepting applications.

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**_About the job_**
Sanofi Manufacturing and Supply organization is preparing its future through an ambitious program named Modulus. The Modulus Project 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 vaccine business challenges as well as Specialty Care Biologics products. One of these two facilities is implemented in Singapore in a new Greenfield site, with a design identical 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 (AGVs), cobots and cloud systems.
This role will have the title of Biotechnologist, Manufacturing and will report to the Manager, Manufacturing. The successful candidate will be part of the pioneer batch of the manufacturing operations shift team who will directly participate in the Engineering and Product Validation Runs in the state-of-the-art facility.
The candidate will have a routine operational role consisting of the following:
+ Perform and complete ongoing commissioning and qualification activities of equipment, digital and automation related systems.
+ Execute routine GMP manufacturing activities in the manufacturing operations team in accordance with Process, Quality and Safety standards.
+ Perform general housekeeping of the manufacturing areas.
+ Support ongoing regulatory and audit readiness and preparation.
+ User of key digital and automation applications and software related to manufacturing systems such as ERP, MES, PCS, etc.
+ Participation in continuous improvement and optimization projects.
Sanofi Modulus Singapore is hiring for Biotechnologist, Manufacturing for the following teams:
+ Upstream Manufacturing Process
+ Downstream Manufacturing Process
+ Central Manufacturing Services (Media & Buffer, Logistics)
**Main responsibilities:**
+ Commissioning and Qualification Activities, Operational Readiness: 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.
+ Tech Transfer: Participate and complete all related trainings to perform the tech transfer runs.
+ cGMP Manufacturing Operations: Perform and participate in the Engineering Runs and other Product Validation Runs
**_About You_**
+ Degree in an Engineering or Science discipline
+ Starting job grade of the role will be commensurate with the applicant's highest education qualification and any other relevant experience.
+ Candidates with prior internships or industrial attachments in biopharmaceutical and biotechnology organizations would be advantageous. -
+ Self-starter and independent worker who can operate and perform in cross functional teams.
+ Possess strong analytical and critical thinking skills with the ability to problem solve and navigate through complexity and ambiguity.
+ Able to work in fast paced and dynamic conditions with tight timelines.
+ Good presentation and verbal communication skills who can adapt and tailor communication to various stakeholders.
+ Excellent technical writing skills
+ Team Player Biotechnologist will be working in a twelve-hour rotating shift pattern consisting of day and night shifts which will include weekend workdays when the facility is fully operational.
**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 (

ABOUT THE JOB

• Supporting biopharmaceutical manufacturing activities across Upstream, Downstream, and Central Services .
• Executing daily production tasks according to schedules, while ensuring strict compliance with cGMP standards .
• Collaborating with cross-functional teams to troubleshoot and resolve technical or process-related issues.
• Accurately documenting all manufacturing activities in line with regulatory and quality requirements .
• Contributing to continuous improvement initiatives aimed at enhancing efficiency, reliability, and safety of manufacturing processes.

ABOUT YOU

• Bachelor's degree in Biotechnology, Chemical Engineering, Pharmaceutical Engineering, or a related discipline.
• Basic understanding of cGMP regulations and biopharmaceutical manufacturing principles.
• Prior exposure to Upstream, Downstream, or Central Services operations (internships, projects, or entry-level roles) is preferred.
• Strong problem-solving mindset, ability to work effectively in fast-paced, team-oriented environments .
• Eager to learn, adapt, and contribute to both client projects and continuous improvement initiatives.

Roles & Responsibilities

Position: Senior Biotechnologist

At Coalesce Management Consulting, we are a community of people with a strong passion for excellence. We deliver bespoke project solutions within the Life Science and Technology sectors through our community of high-calibre industry specialists.

Job Description:

We are currently expanding our team and are looking for a Senior Biotechnologist to work on projects on site with a client. In summary, you will be collaborating with peers to design and validate new experimental techniques, and adhere to rigorous quality control standards to ensure the integrity and purity of cell cultures.

Key Responsibilities:

• Lead and support operations involving DeltaV and DCS Logics, including handshake protocols and prompt configurations
• Manage and optimize Batch Recipe inputs for efficient bioprocess execution
• Execute and optimize chromatography techniques in a downstream processing capacity
• Collaborate cross-functionally to ensure compliance with SOPs and process documentation
• Contribute to the development and refinement of technical workflows and automation strategies
• Ensure compliance with GMP standards and regulatory requirements

Requirements:

• Bachelor's degree in a relevant life science field (e.g., biology, biotechnology, biochemistry). ·
• Min 5 years of relevant working experience in biotechnology or biopharmaceutical manufacturing
• Excellent communication skills, both written and verbal, in English.
• Ability to multitask and work in a fast paced environment with competing priorities.
• Great team player.
• Strong interpersonal and communication skills and ability to develop close working relationships and work collaboratively with internal and external contacts at all levels

What's In It for You?

• Exposure to the major Pharmaceutical Companies in the industry.
• Annual leave benefits.
• Full Health coverage and benefits.
• Training and Development allowance.

What's Next?

If you are interested in applying for this position, please send an email to

Coalesce Management Consulting operates as an equal opportunity employer. No terminology in this advert is intended to discriminate on the grounds of age, race, religion, sexual orientation, or any other factors with no bearing to employment skills and we confirm that we are happy to accept applications from persons of any background for this role.

Tell employers what skills you have

Ability to Multitask
Management Consulting
FMEA
Risk Assessment
GMP
Investigation
Cleaning Validation
Protocol
Python
Communication Skills
Regulatory Requirements
Terminology
Manufacturing
Commissioning
Mapping
Utility Systems

Roles & Responsibilities

Job Description

80%

• Perform loading and Operating of Autoclave

• Responsible for MFR (Manufacturing Formulation Record)/SOP creation and revision

• Perform monitoring for process and equipment performance during operation as per SOP/MFR, identify and report if there's any atypical events

• Support investigation to event and deviation

• Interface with other departments to resolve issues related to daily operations

• Actively support transfer of new processes and commission/validation of new projects

• Actively support Change Control management

10%

The individual will manage equipment and support facility related projects by

• Support routine safety and GMP walk down and responding to findings (If required)

• Support execution of Corrective/Preventive actions which identified (If required)

• Support change control activities which assigned (If required)

• Act as a SME for investigation and solution

• Liaise with other department for Corrective/Preventive actions which identified

• Support shift change/handover activities

10%

Staff Technical Training and Development

• Meet and maintain training requirements

• Complete assigned training on time

• Provide technical training for area personnel

• Provide input on training material development

• Deputize for shift supervisor's activities

• Provide annual performance self-assessment on development plan

• Responsibility to adhere to any applicable EHS requirements.

• Commitment to a fair and respectful relationship to others and behavior in accordance with Code of Conduct.

Education and Experience Requirements

• Min Degree in Biomedical Sciences / Chemical Engineering or related with up to three years of relevant experience in the biotechnology, pharmaceutical industry

• Demonstrate commitment to cGMP, EHS compliance aspects of clean-room and plant operation

• Able to take initiative with good problem solving skills

• Excellent team player with hands-on attitude

• Able to work on rotating shifts

• Ability to lift, pull or push equipment requiring up to 20kg

• Able to climb ladders and work on platforms

• Able to perform confine space entrant/attendant/Supervisor/Assessor (If required)

• Ability to read/understand Safety Data Sheet (SDS) and handle chemicals as per SOP

• Able to monitor and analyze processing parameters to identify atypical trends

• Able to support Continuous Improvement Projects

• Able to perform as a subject matter expert for equipment and/or systems

If you are interested in any of the positions, do kindly drop your most updated resume to and

Thank You.

Leon Leong De Cong

R

Recruit Express Pte Ltd (Healthcare & Lifesciences Division)

EA License: 99C4599

Tell employers what skills you have

Pharmaceutical Industry
Lifesciences
Healthcare
GMP
Investigation
Formulation
Biotechnology
Technical Training
Change Control
Team Player
Manufacturing
Chemical Engineering
Autoclave
EHS