What Sanofi Jobs are in Singapore?

**_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 ( !
We are an R&D driven, AI-powered biopharma company committed to improving people's lives and creating compelling growth. Our team is guided by one purpose: we chase the miracles of science to improve people's lives.
We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world.
Discover more about us visiting or via our movie We are Sanofi ( a career that makes a difference.
Reinvention is in our DNA. It's what drove our evolution from a small French enterprise to one of the world's leading biopharma companies. Whether it's using AI to shorten drug-discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities.
This is where you grow your career. We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people's lives.

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.
**_About the job_**
Our Team:
The Health, Safety and Environment team is a truly worldwide team, built around collaboration with strong values and a team driven by a partnership mindset.
This is an ambitious team which is highly accountable for the workplace safety and compliance of HSE within Sanofi.
Main responsibilities:
+ The Intern will assist in the implementation HSE Corporate initiatives.
+ He/She will need to support the development of HSE improvement project.
+ At the same time, he/she will need to support the team in terms of HSE documentation and site programs.
+ He/She will also be exposed HSE related work matter which may need his/she involvement.
+ Perform site inspection and compilation of observations.
+ Use of digital tools to create promotional video and online quiz
+ Any other HSE related matters
**_About you_**
+ Education: Bachelors/Diploma in Chemical Engineering/ Manufacturing/ Pharmaceutical or similar degree/diploma courses in related field
+ Soft skills: Strong Problem solving, transversal collaboration and communication skills.
+ Technical skills: competent in using Microsoft office, able to perform data analysis
+ Languages: Fluent in English
**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 ( !
We are an R&D driven, AI-powered biopharma company committed to improving people's lives and creating compelling growth. Our team is guided by one purpose: we chase the miracles of science to improve people's lives.
We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world.
Discover more about us visiting or via our movie We are Sanofi ( a career that makes a difference.
Reinvention is in our DNA. It's what drove our evolution from a small French enterprise to one of the world's leading biopharma companies. Whether it's using AI to shorten drug-discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities.
This is where you grow your career. We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people's lives.

**Job Title:** Supervisor, Manufacturing
**Hiring Manager:** Manager, Manufacturing
**Location:** Tuas, Singapore
**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 Modulus 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.
The manufacturing team in Sanofi Modulus, Singapore is seeking to expand the team and has an open position as Supervisor, Manufacturing, responsible for the operations in either **Central Manufacturing Services (CMS)** or **Process Manufacturing (PM)** team.
The role will report to the Manager, Manufacturing. In this role, you will be responsible to lead the startup and operation of the manufacturing areas to produce engineering and PPQ batches with the aim of commercial production. In line with this, you will be responsible to provide field leadership to the team of biotechnologist who will be your direct reports. The working hour of this role is 12-hour rotating shifts (day and night) and also include weekends and public holidays.
The Supervisor, Manufacturing will (not limited to the following):
+ Ensure compliance with GMP, safety regulations, and company procedures.
+ Train, develop, and evaluate team members' performance.
+ Troubleshoot equipment and process issues.
+ Maintain accurate production records and documentation.
+ Initiate and implement continuous improvement initiatives.
+ Manage inventory and resource allocation in the manufacturing operations.
+ Collaborate closely with cross functional teams to operate the manufacturing processmanufacturing process lifecycle and supporting deviation investigations line including management of changes and CAPA implementation, management
+ As a fronter or Subject Matter Expert (SME) to support the team for regulator inspection audits.
**Performance Standards: Duties & Responsibilities**
Key Areas
Action Areas, Deliverables and Outcomes
Weightage (Total 100%)
Team Management and Leadership 50%
Hire, train and manage direct team reports.
Manufacturing Operations 50%
Lead and perform operations on the production floor.
Ensure compliance to applicable HSE and quality guidelines.
**About You**
**Pre-requisites**
+ Knowledge, Skills & Competencies / Language
+ Team management
+ Self-starter and independent worker who can operate and perform in cross functionalsetting.
+ Possess analytical and critical thinking skills with the ability to problem solve andnavigate through complexity and ambiguity.
+ Able to work in fast paced and dynamic conditions with tight timelines.
+ Excellent analytical, consultative, and diagnostic skills with ability to make sound,data-based business decisions.
+ Effective communication skills necessary to interact with internal stakeholders(includes strong presentation skills).
+ Good technical writing skills.
**Qualifications / Requirement**
+ Bachelor's Degree or equivalent with at least 8 years of relevant experience.
+ Biotechnology/Pharmaceutical with At least 2 years of people leadership experience in Manufacturing area.
+ Experience with cGMP documentation and record maintenance.
+ Strong troubleshooting, problem solving and prioritization skills are required.
+ Familiarity and prior working experience with Single Use Systems would be preferred.
+ Previous work experience in a digitalized and automated facility operated by DeltaVand MES would be preferred.
**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 ( !
We are an R&D driven, AI-powered biopharma company committed to improving people's lives and creating compelling growth. Our team is guided by one purpose: we chase the miracles of science to improve people's lives.
We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world.
Discover more about us visiting or via our movie We are Sanofi ( a career that makes a difference.
Reinvention is in our DNA. It's what drove our evolution from a small French enterprise to one of the world's leading biopharma companies. Whether it's using AI to shorten drug-discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities.
This is where you grow your career. We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people's lives.

Sanofi Manufacturing and Supply (M&S) Organization is preparing its future through an ambitious program named Modulus. 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 vaccine business challenges as well as Specialty Care Biologics products. One of these two Modulus Facilities is constructed in Singapore at 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, cobots and cloud systems.
This role will have the title of _Senior 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 planned for early 2026.
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.
+ Conduct Training activities to the team for specific assigned workflows and procedures.
+ Ensure general housekeeping of all 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.
+ Support continuous improvement and optimization projects.
+ Investigate deviations and exceptions including process abnormalities and critical alarms on QMS. Take immediate actions to minimize product and schedule impact.
Sanofi Tuas Singapore is hiring for _Senior Biotechnologist, Manufacturing_ for the following teams:
+ Upstream Manufacturing Process
+ Downstream Manufacturing Process
+ Central Manufacturing Services (Media & Buffer, Logistics)
**Performance Standards: Duties & Responsibilities**
**Key Areas**
**Action Areas, Deliverables and Outcomes**
**Weightage**
**(Total 100%)**
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.
20%
Tech Transfer
+ Participate and complete all related trainings to perform the tech transfer runs.
30%
cGMP Manufacturing Operations
+ Perform and participate in the Engineering Runs and other Product Validation Runs
50%
**Pre-requisites**
**Knowledge, Skills & Competencies / Language**
+ Good communication skills and a team player
+ Proven ability to work as part of an integrated, networked team, and collaborate across functional, organizational, and location boundaries and be people-first values driven
+ Excellent analytical, consultative, and diagnostic skills with ability to make sound, data-based business decisions.
+ Engaging, dynamic
+ Adaptable, relationship focused.
+ Self-organized.
+ Proactive, Result-oriented.
+ Start-up and /or commissioning, qualification of a biopharmaceutical facility would be an advantage.
+ Familiarity and prior working experience with Single Use Systems would be preferred.
+ Good knowledge and experience in related GMP operations based on the manufacturing team.
+ Good knowledge and interest to work with fully digital and automated systems will be preferred. Systems including but not limited to Manufacturing Execution Systems (MES), Enterprise Resource Systems (ERPs), Autonomous Guided Vehicles (AGVs), robotics, conveyor systems, Quality Management Systems (QMS), etc.
**Qualifications / Requirements**
+ Bachelor's degree (in Engineering / Life Science / Biology / Chemistry) with >3 Years of experience in Biopharmaceutical Manufacturing (biologics or vaccines).
+ Diploma (in Engineering / Life Science / Biology / Chemistry) with >5 Years of experience in Biopharmaceutical Manufacturing (biologics or vaccines).
**Any other requirements of the job**
+ Senior 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 expected to be in mid of 2026.
**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 ( !
We are an R&D driven, AI-powered biopharma company committed to improving people's lives and creating compelling growth. Our team is guided by one purpose: we chase the miracles of science to improve people's lives.
We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world.
Discover more about us visiting or via our movie We are Sanofi ( a career that makes a difference.
Reinvention is in our DNA. It's what drove our evolution from a small French enterprise to one of the world's leading biopharma companies. Whether it's using AI to shorten drug-discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities.
This is where you grow your career. We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people's lives.

**About the job:**
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
Sanofi has added two new Modulus Facilities to our global industrial footprint. These production units represent the future of manufacturing. They allow us to increase our capacities while making production more flexible and respectful of the environment.
Fully digitalized, our Modulus Facilities will enable more responsive and flexible manufacturing across multiple vaccine and biological platforms including mRNA, while minimize our impact to the environment. Our facilities will help improve people's lives by giving them faster access to more treatments.
In this context, we are seeking a highly motivated **Quality Control Analyst II (Microbiology)** to join our team and play a key role in establishing and operating a state-of-the-art QC laboratory at our new Singapore site. This position offers an exciting opportunity to contribute to the successful start-up of a new facility and ensure compliance with global quality standards.
**Main Responsibilities**
+ Perform microbiological (including bioburden) and endotoxin test for water, raw materials and product samples
+ Conduct incubation, observation, and accurate recording of test results
+ Execute environmental monitoring activities including viable and non-viable sampling
+ Perform water sampling including Purified water, WFI and clean steam
+ Perform aseptic sample dispensing
+ Write key documents relating to QC (such as SOPs and risk assessments)
+ Participate in method verification for bioburden and endotoxin tests
+ Maintain accurate and complete records in accordance with GMP data integrity requirements
+ Actively contribute to a culture of continuous improvement and quality excellence
**Education and experience**
+ Education: Bachelor's degree or Diploma in Microbiology, Biological Sciences, or a related scientific discipline
+ Experience: Minimum 2-4 years of hands-on laboratory experience in a GMP-regulated pharmaceutical or biotechnology environment
**Key technical competencies and soft skills**
+ Proficiency in aseptic technique and microbiological testing
+ Experience with environmental monitoring programs
+ Knowledge of endotoxin testing methodologies
+ Understanding of GMP regulations and data integrity principles
+ Experience with electronic documentation systems
+ Meticulous approach to testing, documentation, and data review
+ Works effectively within a team and communicates proactively
+ Thrives in a dynamic, fast-paced regulated environment
**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 ( !
We are an R&D driven, AI-powered biopharma company committed to improving people's lives and creating compelling growth. Our team is guided by one purpose: we chase the miracles of science to improve people's lives.
We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world.
Discover more about us visiting or via our movie We are Sanofi ( a career that makes a difference.
Reinvention is in our DNA. It's what drove our evolution from a small French enterprise to one of the world's leading biopharma companies. Whether it's using AI to shorten drug-discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities.
This is where you grow your career. We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people's lives.

**Position: Technician, Quality Control**
+ Hiring Manager: Manager, QC Raw Material & Lab Service
+ Location: Tuas, Singapore
**About the job:**
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
Sanofi has added two new Modulus Facilities to our global industrial footprint. These production units represent the future of manufacturing. They allow us to increase our capacities while making production more flexible and respectful of the environment.
Fully digitalized, our Modulus Facilities will enable more responsive and flexible manufacturing across multiple vaccine and biological platforms including mRNA, while minimize our impact to the environment. Our facilities will help improve people's lives by giving them faster access to more treatments.
In this context, we are looking for one **Quality Control Technician** to participate in the setting up of the new QC laboratory for our new site based in Singapore.
**Key Accountabilities**
The mission described below, must be exercised in compliance with health, safety and environment of the site rules.
+ Support the routine operations of the QC laboratory.
+ Support project execution phase through deliverables achievement and operations activities.
+ Responsible for waste management, including liaising with waste management vendor.
+ Responsible for sample management, including sample receipt, shipment and disposal.
+ Responsible for raw material and drug substance reserve sample management.
+ Responsible for external laboratory coordination and management.
+ Coordinate and perform raw material sampling.
+ Coordinate and perform general laboratory support activities, including procurement and inventory management.
+ Support QC equipment calibration and preventive maintenance program.
+ Participate and contribute to laboratory continuous improvement.
+ Maintain Sanofi standards and values for safety and quality objectives as well as contribute to laboratory performance.
**About you**
**Education and Experience**
+ Higher NITEC with about 2-3 years of experience in QC laboratory operations or fresh graduates with Diploma/Degree in Pharmaceutical Sciences, Applied Science or related life Sciences or Technology.
+ Experience in laboratory support in the pharmaceutical or biotechnology industry preferred.
Key technical competencies and soft skills:
+ Good understanding of good laboratory practices, good documentation practice and data integrity requirements.
+ Experienced in routine laboratory operations and continuous improvements.
+ Keen to learn new technologies.
+ Fluent in English speaking and writing.
**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 ( !
We are an R&D driven, AI-powered biopharma company committed to improving people's lives and creating compelling growth. Our team is guided by one purpose: we chase the miracles of science to improve people's lives.
We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world.
Discover more about us visiting or via our movie We are Sanofi ( a career that makes a difference.
Reinvention is in our DNA. It's what drove our evolution from a small French enterprise to one of the world's leading biopharma companies. Whether it's using AI to shorten drug-discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities.
This is where you grow your career. We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people's lives.

**Job Title:** Validation Engineer
**Hiring Manager:** Senior Manager Validation (Modulus Singapore)
**Location:** Tuas, Singapore
**About the job**
**Mission**
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. The facilities are 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 is responsible for implementing and maintaining qualification and validation strategies, plans, protocols, and reports, in collaboration with internal and external stakeholders.
The role will report to the Senior Manager, Validation. In this role, the (Senior) Validation Engineer, will play a key role in ensuring all equipment, facilities, cleaning and disinfection are properly qualified, validated and maintained in their Q&V status.
**Key accountabilities**
+ Execute qualification and validation plans, protocols, and reports, in collaboration with internal and external stakeholders.
+ Ensure the compliance of qualification and validation with applicable regulatory requirements and company quality standards.
+ Ensure that assigned equipment and facilities are properly qualified; equipment cleaning and sterilization processes (e.g. autoclave, VHP, SIP) as well as surface disinfection (chemical and UV) are properly validated
+ Ensure the proper documentation, review, and approval of qualification and validation deliverables, such as risk assessments, traceability matrices, test scripts, deviations, and summary reports
+ Conduct periodic reviews of validated systems and perform re-validation as necessary.
+ Identify and drive continuous improvement initiatives and projects to enhance the qualification and validation efficiency and effectiveness fostering a culture of continuous improvement
+ Subject matter expert (SME) for validation topics.
+ Lead and participate in equipment investigations to identify root causes and effectively communicate to the stakeholders on the plans and mitigating actions.
+ Perform assessment for equipment during new product introduction, change controls and other qualifications activities to ensure equipment are in its validated state.
+ Actively seek opportunities for continuous improvement through use of new technologies and best industry practices as well as establishing framework for validation.

**Scope and dimensions**
+ Breadth of responsibility (global and site):
+ Scope is local, focus primarily on activities in Sanofi Tuas site, with some transversal engagement with product donor site or Global experts.
+ Impact on defining, designing, and implementing the framework and best practices for validation lifecycle management.
+ Various interactions specifically with Manufacturing Operations, Quality, MSAT teams and beyond with all project functions involved in the process approach definition (HSE, Quality, Digital, Supply chain) as well as with external contractors and suppliers.
**About you**
**Skills and knowledge expected**
+ Good knowledge of commissioning and qualification activities including use of Kneat
+ Good shopfloor and operational knowledge of GMP, Validation and Biopharmaceutical processes including use of single-use technologies
+ Good communication skills and a team player
+ Proven ability to work as part of an integrated, networked team, and collaborate across functional, organizational, and location boundaries and be people-first values driven
+ Excellent analytical, consultative, and diagnostic skills with ability to make sound, data-based business decisions
+ Engaging, dynamic
+ Adaptable, relationship focused
+ Self-organized
+ Proactive, Result-oriented
**Education and experience**
+ Experiences in Validation and biotech manufacturing or process engineering
+ Demonstrated experience in driving innovation and change to improve efficiencies
+ Bachelor's degree in Engineering, with at least 4 years of related experience
+ Fluent in English (writing and speaking)
**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 ( !
We are an R&D driven, AI-powered biopharma company committed to improving people's lives and creating compelling growth. Our team is guided by one purpose: we chase the miracles of science to improve people's lives.
We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world.
Discover more about us visiting or via our movie We are Sanofi ( a career that makes a difference.
Reinvention is in our DNA. It's what drove our evolution from a small French enterprise to one of the world's leading biopharma companies. Whether it's using AI to shorten drug-discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities.
This is where you grow your career. We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people's lives.

**Job Title:** Supply Chain Intern
**Location:** Tuas
**Reports To:** Head of Supply Chain
**Employment Type:** Internship (Full-time)
**About the Role**
The Modulus Singapore Supply Chain Intern will support the supply chain team in delivering data-driven insights to improve site supply planning and logistics processes. The intern will contribute to building a resilient and adaptable supply chain capable of supporting NPI materials through to commercial supply. Working closely with cross-functional teams including production, manufacturing technology, engineering, safety, and quality, the intern will play an active role in implementing a fit-for-purpose supply & logistics operating model.
**Key Responsibilities**
+ Support the supply chain team in designing and implementing fit-for-purpose supply & logistics strategies
+ Maintain and manage supply planning and material master data; during the project phase, act as supply chain user representative for master data setup, planning parameter definition, UAT, and training development
+ Design and set up reporting metrics for internal performance monitoring and external service providers (e.g. on-time delivery, order fulfillment rates, inventory turns)
+ Build and maintain dashboards and reports using data visualization tools (e.g. Power BI, Excel) to deliver actionable supply chain insights
+ Support value stream mapping to identify process gaps, waste, and improvement opportunities
+ Derive insights from logistics data across availability, sourcing, distribution, and supplier management
+ Ensure adherence to cGMP and all Sanofi Quality, Safety, and Compliance requirements
+ Explore and promote adoption of AI and digital tools within the supply chain function
**What You Bring**
+ Pursuing a degree in Supply Chain Management, Industrial Engineering, Business Analytics, or related field
+ Strong analytical and critical thinking skills
+ Proficiency in Microsoft Excel; experience with Power BI or Tableau is a plus
+ Familiarity with ERP systems (e.g. SAP) and lean/VSM concepts is advantageous
+ Eager to learn new technologies and digital tools including AI
+ Ability to work effectively in multi-disciplinary, multi-cultural teams
+ Detail-oriented, proactive, and a strong team player
**What We Offer**
+ Hands-on exposure to both NPI and commercial supply chain operations
+ Opportunity to contribute to a greenfield project at Modulus Singapore
+ Mentorship from experienced supply chain professionals
+ Access to cutting-edge AI and digital tools in a global pharmaceutical environment
**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 ( !
We are an R&D driven, AI-powered biopharma company committed to improving people's lives and creating compelling growth. Our team is guided by one purpose: we chase the miracles of science to improve people's lives.
We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world.
Discover more about us visiting or via our movie We are Sanofi ( a career that makes a difference.
Reinvention is in our DNA. It's what drove our evolution from a small French enterprise to one of the world's leading biopharma companies. Whether it's using AI to shorten drug-discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities.
This is where you grow your career. We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people's lives.

**About the job:**
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
Sanofi has added two new Modulus Facilities to our global industrial footprint. These production units represent the future of manufacturing. They allow us to increase our capacities while making production more flexible and respectful of the environment.
Fully digitalized, our Modulus Facilities will enable more responsive and flexible manufacturing across multiple vaccine and biological platforms including mRNA, while minimize our impact to the environment. Our facilities will help improve people's lives by giving them faster access to more treatments.
In this context, we are seeking a highly motivated **Quality Control Analyst I (Microbiology)** to join our team and play a key role in establishing and operating a state-of-the-art QC laboratory at our new Singapore site. This position offers an exciting opportunity to contribute to the successful start-up of a new facility and ensure compliance with global quality standards.
**Main Responsibilities**
+ Perform microbiological (including bioburden) and endotoxin test for water, raw materials and product samples
+ Conduct incubation, observation, and accurate recording of test results
+ Execute environmental monitoring activities including viable and non-viable sampling
+ Perform water sampling including Purified water, WFI and clean steam
+ Perform aseptic sample dispensing
+ Write key documents relating to QC (such as SOPs and risk assessments)
+ Maintain accurate and complete records in accordance with GMP data integrity requirements
+ Actively contribute to a culture of continuous improvement and quality excellence
**Education and experience**
+ Education: Bachelor's degree or Diploma in Microbiology, Biological Sciences, or a related scientific discipline
+ Experience: Graduate or professional with 1-2 years of hands-on laboratory experience in a GMP-regulated pharmaceutical or biotechnology setting
**Key technical competencies and soft skills**
+ Proficiency in aseptic technique and microbiological testing
+ Experience with environmental monitoring programs
+ Knowledge of endotoxin testing methodologies
+ Understanding of GMP regulations and data integrity principles
+ Experience with electronic documentation systems
+ Meticulous approach to testing, documentation, and data review
+ Works effectively within a team and communicates proactively
+ Thrives in a dynamic, fast-paced regulated environment
**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 ( !
We are an R&D driven, AI-powered biopharma company committed to improving people's lives and creating compelling growth. Our team is guided by one purpose: we chase the miracles of science to improve people's lives.
We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world.
Discover more about us visiting or via our movie We are Sanofi ( a career that makes a difference.
Reinvention is in our DNA. It's what drove our evolution from a small French enterprise to one of the world's leading biopharma companies. Whether it's using AI to shorten drug-discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities.
This is where you grow your career. We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people's lives.