41 jobs in Sanofi Group

Career Conversion Programmes (CCPs) support mid-career new hires, existing employees or fresh graduates seeking to transition into growth job roles with good longer-term prospects through structured on-the-job training. The program is for 15 months with WSG and Sanofi.
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.
**About the Job**
Having successfully completed commissioning and qualification, the Singapore facility is now in routine manufacturing operations. This role will have the title of Biotechnologist Trainee and will report to the Manufacturing Supervisor. The successful candidate will be part of the manufacturing operations shift team, contributing to steady-state production across Upstream, Downstream, and Central Manufacturing Services (CMS) processes in this state-of-the-art facility.
The candidate will have a routine operational role consisting of the following:
+ Execute routine cGMP manufacturing activities within the Upstream, Downstream, or CMS (Media & Buffer, Logistics) teams, in accordance with Process, Quality and Safety standards.
+ Operate and monitor manufacturing equipment, digital and automation systems in day-to-day production runs.
+ Perform general housekeeping of the manufacturing areas.
+ Maintain ongoing regulatory and audit readiness through consistent adherence to procedures and documentation standards.
+ Act as a key user of digital and automation applications and software supporting manufacturing systems such as ERP, MES, PCS, etc.
+ Participate in continuous improvement and optimization initiatives to enhance routine operational efficiency.
+ Support batch documentation, deviation reporting, and change control activities as part of routine operations.
Sanofi Modulus Singapore is hiring for Biotechnologist Trainee for the following teams:
+ Upstream Manufacturing Process
+ Downstream Manufacturing Process
+ Central Manufacturing Services (Media & Buffer, Logistics)
Main responsibilities:
+ Routine Manufacturing Operations: Perform day-to-day production activities within Upstream, Downstream, or CMS, ensuring compliance with process, quality, and safety requirements.
+ Documentation & Compliance: Maintain and follow standard operating procedures, risk assessments, and training records for manufacturing equipment and systems.
+ Digital & Automation Systems: Operate and troubleshoot digital/automation tools integrated into daily manufacturing processes.
+ cGMP Manufacturing Execution: Support routine batch production, in-process checks, and quality documentation in line with cGMP standards.
+ Continuous Improvement: Identify and contribute to process optimization opportunities within the assigned Upstream, Downstream, or CMS area.
**About You**
+ NITEC/Diploma 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.
**Job Location:**
Sanofi Aventis Singapore - 5 Tuas South Street 2, Singapore
**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.

Launch Your Career Where It Matters Most
What if your internship could directly contribute to protecting lives - not just in the lab, but on the ground, every single day? At Sanofi, we believe that safety and sustainability aren't just compliance checkboxes - they are the foundation of everything we do. As our next **HSE Intern** , you won't be fetching coffee or sitting on the sidelines. You'll be embedded in a high-performing team, tackling real challenges, and leaving a measurable impact on our operations.
This is your opportunity to step into the pharmaceutical industry with purpose, build expertise that sets you apart, and work alongside professionals who are passionate about making the world a safer, cleaner place.
Why This Internship Is Different
Most internships give you a glimpse. This one gives you the **full picture** .
You'll gain hands-on exposure across four dynamic functional areas that form the backbone of world-class HSE operations:
+ **HSE Fieldwork** - Get out of the classroom and into the field. Experience both **field safety and process safety** in a live operational environment, seeing firsthand how safety principles protect people and processes at scale.
+ **HSE Compliance** - Discover how critical documentation drives compliance, accountability, and continuous improvement across a global pharmaceutical operation.
+ **Corporate Sustainability Reporting** - Contribute to Sanofi's environmental mission by working on real sustainability metrics - **waste, energy, water, and cooling** - that feed directly into corporate-level decision-making.
+ **Training & Development Programs** - Help design and deliver in-house HSE training, create safety induction video, shaping the safety culture of an entire site.
Your Mission: Real Responsibilities, Real Impact
You won't be handed a theoretical project and left alone. You'll be an active contributor to initiatives that keep our people safe and our operations sustainable. Here's what you'll own:
️ Operations & Engineering
+ Contribute to **ATEX Compliance Survey** , applying your engineering knowledge to solve real operational challenges
Environmental Reporting
+ Produce **reports** on waste, energy, water, and cooling - ensuring our operations remain fully compliant with environmental standards and your numbers will inform decisions at the highest levels of the organization
️ Safety Initiatives
+ Support **field safety and process safety initiatives** that protect every person who walks through our doors
+ Create **safety induction video** with the **10 life-saving rules**
+ Lead or contribute to at least **one impactful HSE improvement project** , complete with your own documented findings and recommendations - a portfolio piece you'll be proud to show future employers
Compliance & Documentation
+ Perform gap assessments for revised **Sanofi standards** and **ISO14001:2026** to ensure **documents are current, accurate, and audit-ready** , playing a direct role in keeping the site compliant with regulatory standards
+ Prepare documentation that stands up to the scrutiny of **formal audits and inspections**
Training & Culture
+ Help **organize and execute HSE training sessions, Safety Campaigns** for staff across the site, contributing to a culture where safety knowledge is shared, documented, and continuously improved
What You'll Walk Away With
By the end of this internship, you won't just have a line on your CV - you'll have a **toolkit of industry-relevant skills** that accelerate your career:
Deep understanding of **pharmaceutical industry processes and equipment**
Practical knowledge of **HSE department operations** , from field safety to process safety management
Hands-on **experience** and insight into how complex projects are executed in a regulated environment
Exposure to **corporate sustainability frameworks** and environmental reporting at an international scale
A professional network within one of the world's leading pharmaceutical companies
Who We're Looking For
You're ambitious, curious, and ready to roll up your sleeves. You want an internship that challenges you and prepares you for a career that makes a difference.
**You're studying toward a degree in:**
- Chemical Engineering
- Manufacturing Engineering
- Pharmaceutical Sciences
- Or a closely related discipline
You don't need to have all the answers - you just need the drive to find them.
Ready to Make Your Mark?
At Sanofi, our mission is to chase the miracles of science to improve people's lives. Every safe operation, every sustainability milestone, and every well-trained employee brings us closer to that mission. As our HSE Intern, **you'll be part of that story** .
_> *"The best way to predict your future is to create it."* - Join us, and start creating yours._
**Apply now and take the first step toward a career that protects people, preserves our planet, and powers the future of healthcare**
**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**
Sanofi (Tuas) is seeking a motivated and detail-oriented Procurement Intern to join our Procurement team.
This internship offers a valuable opportunity to gain hands-on experience in a dynamic, fast-paced procurement environment within a leading global pharmaceutical company.
The successful candidate will support the procurement team in day-to-day operations, vendor management, and strategic sourcing activities, contributing to Sanofi's mission of delivering health solutions to patients worldwide.
Key Responsibilities
+ Support Procurement Site Lead for the consolidation, prioritization and value creation of all third party spend of Sanofi Modulus Tuas site
+ Collaborate cross-functionally with Key Supplier Operational Leader, Finance, Supply Chain and Global Lead Buyers as required
+ Support Procurement and KSOL in vendor management activities, including maintaining supplier databases and tracking vendor performance
+ Lead, attend meetings (internal and vendor) representing Procurement during the absence of Procurement Site Lead
+ Conduct online research and supplier evaluations to support sourcing decisions and identify potential new vendors
+ Assist in the preparation of procurement reports, dashboards, and presentations for internal stakeholders
+ Provide Procurement related administrative support such as organising vendor interactions, preparing meeting minutes, and timely update of Procurement trackers
**About You**
Required Qualifications
+ Degree or Diploma preferably in Supply Chain Management, Business Administration, or a related field
+ Previous internship or work experience in any field
+ Candidates from Polytechnic or University programmes are welcome to apply
+ Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint), Power BI, Data Analysis
Preferred Qualifications
+ Basic knowledge of procurement processes, supply chain concepts, or sourcing strategies
+ Familiarity with any procurement systems or ERP software (e.g., SAP, Ariba, Oracle)
+ Strong organisational and time management skills with the ability to manage multiple tasks simultaneously
+ Excellent written and verbal communication skills
What We Offer
+ Hands-on experience in a global multinational bio-pharmaceutical company's brand new Modulus facility, a highly automated biopharma factory of the future
+ Exposure to end-to-end procurement processes and best practices
+ Mentorship and guidance from experienced procurement professionals
+ Opportunity to build a professional network across functions and geographies
+ A collaborative, inclusive, and supportive work environment
+ Competitive internship allowance
**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**
Sanofi Manufacturing and Supply is shaping the future of biologics manufacturing through **Modulus** , an ambitious program at the heart of Sanofi's strategy. The Modulus Project is creating a new generation of evolutive, multi-product manufacturing facilities that are modular, adaptable, and agile, leveraging innovative technologies to better support vaccine and Specialty Care Biologics manufacturing.
**Accountabilities**
**Tier 3 Project Support & Coordination**
+ Provide project feasibility evaluation and technical front-end studies input to support decision-making process with site leadership team
+ Coordinate technical inputs across multiple engineering functions (automation, electrical & instrumentation, mechanical, utilities and sustainability) for Tier 3 projects
+ Serve as single point of contact for projects requiring multi-disciplinary engineering support; facilitate cross-functional engineering reviews and ensure alignment between project requirements and site capabilities. Consolidate and communicate engineering recommendations to project stakeholders and site leadership
+ Lead and support project sourcing and 3rd party contractor & supplier management to support capital project delivery
+ Provide support to Manufacturing, Engineering and Tier 3 Capital Projects as required
**Manufacturing-Engineering Interface**
+ Act as technical liaison between Manufacturing (biotechnologists) and Engineering & Maintenance department for equipment and automation troubleshooting
+ Provide advanced technical support to diagnose and resolve complex system issues, minimizing downtime. Decide on advanced troubleshooting methods and issue resolution strategies
+ Communicate issues and resolutions to management, peers and engineering team
+ Translate manufacturing operational issues into technical specifications for engineering teams
+ Bridge communication gaps between process operations and engineering disciplines to ensure effective problem-solving
+ Identify improvement opportunities for critical systems, advise on process improvement initiatives
+ Implementing process improvements to enhance efficiency, safety, and quality
+ Participate and provide technical advice in deviation and root cause investigations
**Technical Excellence & Knowledge Management**
+ Advise on system lifecycle changes, including upgrades, decommissioning, and revalidation requirements
+ Support T1 & T2 (Global Engineering) project integration to site routine, inclusive of technical/project support post qualification and handover to site
+ Capture and institutionalize equipment expertise and maintenance know-how during project handovers from Global Engineering (T1 & T2)
**Education**
+ Degree in Engineering (Chemical / Mechanical / Pharmaceutical / Industrial & Systems)
**Experience, Knowledge and Skills**
+ Only candidate with sound technical knowledge and **hands-on** equipment/process troubleshooting, and equipment commissioning experience should apply
+ Only candidate with prior GxP experience should apply
+ Minimum 3 years for specialist and 6 years for (senior) engineer with experience in Process Engineering, Project Management and Equipment commissioning in biopharmaceuticals or API manufacturing
+ Strong knowledge in process engineering, equipment (DeltaV) automation and instrumentation
+ Experience in frontend feasibility studies, project execution
+ PMP certification will be an advantage
+ Excellent analytical and problem-solving skills to address technical issues.
+ Strong stakeholder & people management skills; ability to efficiently work and deliver high performance in cross-functional matrix organization
**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_**
Sanofi Manufacturing and Supply organization is preparing its future through an ambitious program named Modulus. The Modulus Project is at the cornerstone of Sanofi's strategy, creating a new generation of evolutive, multi-product manufacturing facilities that are modular, adaptable and agile, leveraging disruptive technologies to better address vaccine and Specialty Care Biologics manufacturing needs.
As the **Head of SMS Program** , you will lead the deployment, governance and continuous evolution of the Sanofi Manufacturing System (SMS) across the site. You will be responsible for driving operational excellence, enabling sustainable performance improvements, embedding standardized operating practices, and strengthening continuous improvement capabilities while partnering closely with Site Leadership, Global SMS teams and cross-functional stakeholders.
**As a Head of SMS Program, you will be:**
**Driving site performance and transformation**
+ Lead the deployment and continuous evolution of the Sanofi Manufacturing System (SMS 2.0) across the site.
+ Drive performance transformation initiatives including SMS deployment, performance boosters, continuous improvement programs and Factory 4.0 solutions.
+ Identify operational performance gaps through benchmarking, maturity assessments and data-driven analysis, translating insights into improvement opportunities.
+ Ensure performance initiatives deliver measurable business impact across Quality, Delivery, Cost, Safety and People objectives.
+ Lead change management activities to embed sustainable operational excellence practices across the organization.
**Ensuring impact and sustainability**
+ Establish governance to monitor initiative progress, benefits realization and long-term sustainability.
+ Drive value realization by partnering with Finance, Operations and Procurement to validate and capture savings generated through transformation initiatives.
+ Monitor performance indicators and proactively identify risks requiring corrective actions.
+ Ensure continuous improvement initiatives are standardized, sustained and replicated where applicable across the manufacturing organization.
**Developing SMS operating standards and capabilities**
+ Partner closely with Global SMS ecosystem leaders to develop, deploy and continuously improve SMS operating standards.
+ Support Manufacturing & Supply network initiatives including SMS Maturity Assessments, SMS Trainer activities and cross-site knowledge sharing.
+ Lead the site's SMS capability building strategy by developing structured upskilling roadmaps and continuous learning programs.
+ Foster a culture of operational excellence through coaching, mentoring and capability development at all organizational levels.
**Leading governance and decision making**
+ Manage resource allocation for performance and transformation initiatives.
+ Oversee the site digital budget supporting SMS deployment and Factory 4.0 initiatives.
+ Define execution approaches for operational excellence programs and transformation initiatives.
+ Establish expected value creation targets and confirm realization of business benefits.
+ Lead the development of the site's SMS capability roadmap.
+ Drive periodic reviews and annual upgrades of SMS operating standards in partnership with Global Manufacturing & Supply teams.
**_About You_**
**Experience**
+ Minimum 8 years of experience leading Operational Excellence, Lean, Six Sigma or Continuous Improvement programs within the pharmaceutical or other highly regulated manufacturing industries.
+ Proven experience leading transformation and change management initiatives.
+ Demonstrated experience deploying manufacturing operating systems and driving sustainable operational performance improvements.
+ Experience working within cGMP regulated manufacturing environments.
**Technical & Functional Skills**
+ Strong knowledge of Sanofi Manufacturing System (SMS) operating standards and SMS certification framework preferred.
+ Expertise in Operational Excellence methodologies including Lean Manufacturing, Six Sigma, Agile and Continuous Improvement.
+ Strong understanding of manufacturing financial performance including Profit & Loss, Gross Margin, Cost of Goods Sold (COGS), Business Operating Income (BOI), cash flow and project portfolio management.
+ Knowledge of performance management methodologies and tools including 3P and Shine.
+ Good understanding of data management and digital products supporting SMS operating standards, including eOEE, FaCT and iObeya.
+ Strong project management, stakeholder management and communication skills.
+ Good understanding of cGMP requirements and pharmaceutical manufacturing processes.
**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.
**Main responsibilities:**
+ Being representative of the site in the Business Operating Communities (BOC) related to QC digital core models, led by the global, in his/her scope and ensuring local communication.
+ Executing local deployments of QC digital solutions (core model and local), in accordance with defined deployment plans and validation protocols.
+ Issuing all local documentation related to QC digital solutions in scope, required to ensure their usage and maintenance in an appropriate way.
+ Providing training and support of end-users on QC digital tools (in coordination with Sanofi global teams for core models).
+ Maintaining and updating master data and end-user access to the QC digital tools, according to defined requirements and documentation.
+ Informing his/her manager of any event related to digital systems in scope in a timely manner to ensure investigation and impact assessment are performed appropriately.
+ Participating actively to any investigation, where he/she is involved, to ensure investigations and impact assessment are performed appropriately.
+ Executing assigned CAPAs related to remediation plans, mitigation plans and continuous improvements.
+ Support annual method review in the framework of annual product review
+ Support the invalid assay trending program in the QC laboratory.
+ Lead compendial compliance assessment and adherence for the QC laboratory.
+ Lead periodic analytical method control trend review/ investigation and data evaluation on method performance, recommend method improvements where appropriate.
+ Support the execution of qualification and maintenance operations related to QC equipment of the quality control laboratory to ensure adherence to the committed scheduled plans.
+ Ensuring all **QC equipment are properly qualified and maintained** for their intended use.
+ Contribute to the **compliance of laboratory GXP asset qualification and maintenance** with applicable regulatory requirements and company quality standards.
+ Contribute to the proper documentation, issuance, review, and approval of **qualification and maintenance deliverables** , such as risk assessments, traceability matrices, protocols, reports, deviations, and summary reports.
+ **Investigating** on a timely manner **and resolving** any quality control events, issues or discrepancies from his/her perimeter. Implementing remediation actions from findings and CAPAs.
+ **Providing support** during regulatory inspections and audits by presenting equipment management and Method validation documents and records **.**
+ Leading initiatives for **continuous improvement** in QC support processes related to lab equipment management.
+ Writing/reviewing protocols, user acceptance test (UAT) and reports related to analytical validation/transfers and qualification activities.
+ Participate in Change Control Request facilitation and management in relation to QC test methods.
+ Provide technical system administrator support for QC GXP laboratory computerized systems.
+ Assume role of SME for Labware LIMS and collaborate closely with global site functions to address changes
+ Ensuring laboratory instruments and facilities are kept in a quality and safety status to ensure that they can be used appropriately.
+ Recording all expected raw data, calculations, information, related to his/her tasks, to comply with cGMP and Data integrity requirements.
+ Performing his/her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records, related to these tasks.
**_About you_**
+ _Bachelor's degree in Chemistry, Pharmaceutical Science, Biotechnology, Engineering, or a related field._
+ _Relevant experience in pharmaceutical Quality Control or a regulated GxP laboratory environment._
+ _Experience with QC digital systems, LIMS, computerized systems, equipment qualification, analytical method validation, or method transfer._
+ _Good knowledge of cGMP, data integrity, deviation, CAPA, change control, and validation requirements._
+ _Strong analytical, documentation, communication, and stakeholder management skills._
+ _Able to work independently, support end users, deliver training, and collaborate with local and global teams._
+ _Fluent in written and spoken English._
_Why choose us?_
+ Bring the miracles of science to life alongside a supportive, future-focused team.
+ Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
+ Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
+ Take good care of yourself and your family, with a wide range of health and wellbeing benefits including health insurance, out-patient benefits along with a range of family friendly policies such as maternity, paternity, and solo parent leaves to name a few.
**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**
Sanofi Manufacturing and Supply organization is preparing its future through an ambitious program named **Modulus** . The Modulus Project is at the cornerstone of Sanofi's 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.
As a **Metrology & Periodic Qualification Technician (Electrical & Instrumentation)** , you will play a critical role in ensuring the reliability, accuracy and compliance of electrical systems and process instrumentation across the manufacturing facility. You will be responsible for executing preventive and corrective maintenance, calibration and periodic qualification activities to maximize equipment availability while ensuring compliance with cGMP, regulatory requirements and Engineering standards. You will also support the site's digital transformation initiatives by maintaining highly reliable utility and process equipment that enable safe and uninterrupted manufacturing operations.
**Responsibilities :**
+ Operate, maintain and troubleshoot electrical distribution systems, including HT and LV switchboards, distribution panels, ELV systems and process instrumentation to maximize plant availability.
+ Perform calibration, periodic qualification, maintenance and repair of process and utility instrumentation to ensure equipment reliability and regulatory compliance.
+ Execute preventive, corrective and breakdown maintenance activities in accordance with approved maintenance plans, Standard Operating Procedures (SOPs) and Computerized Maintenance Management System (CMMS) work orders.
+ Plan, schedule and complete maintenance activities while ensuring timely closure of work orders and accurate maintenance documentation.
+ Support commissioning, qualification and handover activities for new facilities, utilities, equipment and electrical systems.
+ Support engineering projects, plant modifications and continuous improvement initiatives to enhance equipment reliability and operational efficiency.
+ Manage critical spare parts for electrical and instrumentation equipment to ensure business continuity.
+ Develop and maintain maintenance procedures, calibration documentation, technical records and training materials.
+ Ensure all maintenance activities comply with cGMP, GDP, EHS requirements, Sanofi Engineering Standards and applicable Singapore electrical standards.
+ Support investigations relating to deviations, CAPAs, maintenance events and equipment failures.
+ Support internal and external regulatory inspections, including FDA, EMA and HSA audits.
+ Coordinate and supervise contractors and vendors to ensure maintenance and project activities are completed safely, on schedule and in compliance with quality standards.
+ Collaborate closely with Automation, Manufacturing, Process Engineering, Quality, Digital and Engineering teams to support reliable manufacturing operations and Industry 4.0 initiatives.
+ Promote a **Safety First, Quality Always** culture while driving continuous improvement across engineering and maintenance activities.
**About You** **:**
**Experience**
+ Diploma or Advanced Diploma in Electrical Engineering, Instrumentation Engineering or a related technical discipline.
+ Minimum **8 years of experience** in Electrical & Instrumentation maintenance, calibration and metrology within pharmaceutical or other highly regulated manufacturing environments.
+ Experience maintaining HT, LV, ELV systems and process instrumentation.
+ Experience performing commissioning, qualification and calibration activities for utility and manufacturing equipment.
+ Experience managing preventive maintenance, corrective maintenance, deviations, CAPAs and CMMS work orders.
+ Experience supporting regulatory inspections and audits within cGMP-regulated manufacturing environments.
+ Experience coordinating contractors and supporting engineering projects.
**Technical Skills**
+ Strong knowledge of Electrical & Instrumentation systems, calibration principles and maintenance best practices.
+ Good understanding of Singapore electrical standards (SS650, SS638) and applicable statutory requirements.
+ Ability to interpret Single Line Diagrams (SLDs), P&IDs, electrical schematics and instrumentation drawings.
+ Good knowledge of pharmaceutical utilities, manufacturing equipment and process instrumentation.
+ Familiarity with Computerized Maintenance Management Systems (CMMS).
+ Strong troubleshooting, analytical and problem-solving skills.
+ Good understanding of cGMP, GDP, EHS and pharmaceutical regulatory requirements.
+ LEW Grade 7 certification will be an added advantage.
+ Strong communication and stakeholder management skills with the ability to work collaboratively across cross-functional teams.
+ Demonstrated commitment to operational excellence, continuous improvement and digital manufacturing initiatives.
**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.

**_About the Job:_**
The Qualification & Validation team, within the Quality function, provides quality oversight of system and process validation lifecycle activities, ensuring compliance with Sanofi quality standards and regulatory requirements.
Our team is responsible for quality oversight of validation activities across a broad scope, including:
+ **Facilities, Utilities & Equipment (FUE)**
+ **Computerized Systems**
+ **Manufacturing Processes**
+ **Decontamination Methods** (sterilization, cleaning, and disinfection)
+ **Transportation**
+ **Analytical Instruments & Procedures**
The team also provides quality oversight of **technology transfer activities** .
**The Role**
As a Qualification & Validation Specialist, you will be a key member of the Qualification & Validation team, serving as a trusted quality partner for validation lifecycle activities at our Singapore Tuas manufacturing site. This role is central to ensuring that our facilities, systems, and processes are qualified and validated to the highest standards - directly safeguarding the quality, safety, and efficacy of the medicines we deliver to patients.
You will work at the intersection of quality, engineering, and manufacturing - applying your technical expertise and risk-based thinking to evaluate, challenge, and approve validation activities. You will be expected to exercise sound judgment in assessing compliance with regulatory requirements and Sanofi quality standards, while collaborating closely with cross-functional teams to drive timely execution of validation deliverables.
This is a role for someone who thrives in a dynamic, regulated environment and is passionate about upholding the highest standards of pharmaceutical quality.
**_What You'll Do:_**
As a Qualification & Validation Specialist, you will play a critical role in ensuring that all qualification and validation activities meet the highest standards of quality and regulatory compliance. Your main accountabilities will include:
+ **Quality Oversight** - Provide quality oversight of qualification and validation tasks within your assigned area, ensuring all activities are executed in accordance with Sanofi standards
+ **Documentation** - Prepare and review qualification and validation documentation, including protocols, reports, risk assessments, and traceability matrices, adhering to pre-defined timelines
+ **Deviation Management** - Ensure proper documentation of deviations, non-conformances, and corrective actions
+ **Change Control** - Evaluate change controls with validation expertise to ensure quality and compliance
+ **Regulatory Compliance** - Ensure all qualification and validation activities comply with regulatory requirements (e.g., FDA, EMA) and Sanofi quality standards
+ **Audit & Inspection Support** - Participate in internal and external audits and health authority inspections, providing necessary documentation and expert support
+ **Cross-functional Collaboration** - Work closely with engineering, manufacturing, and quality control teams to ensure smooth execution of validation activities
+ **Continuous Improvement** - Identify opportunities to improve qualification and validation processes and contribute to ongoing improvement initiatives
**_About You:_**
**Education**
+ Bachelor's degree or higher in **Science, Engineering, Pharmacy** , or a related discipline
+ Additional certifications in Quality Management, Validation, or GMP (Good Manufacturing Practice) are advantageous
**Experience**
+ A minimum **5-7 years of experience** in qualification and validation within the pharmaceutical, biotechnology, or related regulated industry
+ Hands-on experience with validation of: Facilities, Utilities & Equipment (FUE), computerized systems, manufacturing processes, cleaning/sterilization/disinfection methods
+ Experience supporting **regulatory inspections** and **internal/external audits**
+ Familiarity with **technology transfer** activities is a plus
**Technical Competencies**
+ **Regulatory & Industry Standards:** Sound knowledge and understanding of regulatory requirements and industry best practices (e.g., FDA, EMA, ICH, ISO, ASTM, ISPE, PDA) pertaining to management of validation lifecycle
+ **Documentation:** Proficiency in preparing and reviewing validation documentation, including Validation Master Plans, Protocols and Reports (IQ, OQ, PQ), Risk Assessments (e.g., FMEA), Traceability Matrices
+ **Quality Risk Management:** Working knowledge of quality risk management methods and tools, including Failure Mode Effects Analysis (FMEA), Hazard Analysis and Critical Control Points (HACCP), Fault Tree Analysis (FTA), and their application to validation of systems.
+ **Risk- and Science-Based Validation:** Solid technical knowledge in the use and application of **risk-based** and **science-based** approaches to validation, aligned with ICH Q9 and modern validation principles
+ **Quality Systems:** Experience with **deviation handling** , **CAPA management** , and **change control** processes
+ **Paperless validation Tools:** Familiarity with electronic document management systems (e.g., Kneat, Veeva) is an advantage
**Soft Skills**
+ **Communication** : Excellent written and verbal communication skills; able to articulate complex validation concepts clearly
+ **Collaboration** : Strong team player with the ability to work effectively across functions (Engineering, Manufacturing, QC, QA)
+ **Independence & Initiative** : Able to work independently with minimal supervision while maintaining high standards of quality and compliance
+ **Time Management** : Ability to manage multiple priorities and deliver within pre-defined timelines
+ **Continuous Improvement Mindset** : Proactive in identifying opportunities to enhance validation processes and practices, and drive quality excellence
**What Sets You Apart**
+ Experience in **biologics** , **sterile or aseptic manufacturing** environments
+ Exposure to **Health Authority inspections** (e.g., HSA, FDA, EMA)
+ Knowledge of **data integrity** principles (ALCOA+)
+ Familiarity with **Sanofi quality systems and standards**
**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.