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Showing 866 Qa Consulting jobs in Singapore
Job Description
**Specialist Quality Assurance**
**Amgen Singapore Manufacturing**
**HOW MIGHT YOU DEFY IMAGINATION?**
Amgen is one of the world's leading independent biotechnology companies. For over 4 decades, Amgen has pioneered biotechnology breakthroughs, to bring state-of-the-art medicines from laboratory to the patient. Amgen has not only discovered and developed innovative human therapeutics but has invested in cutting edge manufacturing capability and support services to deliver these exciting therapies to medical teams around the world. Japan and Asia Pacific (JAPAC) is the fastest growing region in Amgen. Now we are hiring a **Specialist Quality Assurance** in **Amgen Singapore Manufacturing.**
**Live**
**What you will do**
Responsible for providing oversight and leadership for quality systems execution and operations support, the Specialist Quality Assurance will support manufacturing operations and IPC testing through presence on the floor, and support of complex manufacturing investigations, change control, and unexpected result investigations.
Main Responsibilities:
+ Provide Quality oversight to plant operations, ensuring appropriate application and execution of GMP compliance requirements and Amgen Quality Management System in plant operations through phases of commissioning, process qualification, regulatory approval and market supply
+ Support routine GMP documentation review activities (e.g. electronic batch records, SOPs, logbooks, work orders, batch production reports and validation protocols etc.) and ensure key performance indicator met targeted metrics
+ Co-lead and support the deployment of Amgen quality systems, including management review, validation, change control and CAPA and ensure that the systems are managed in compliance with cGMP expectations
+ Participate in complex root cause investigations for deviations
+ Review and approve deviation investigations, change controls, and other quality records (with focus on highly complex records)
+ Provides Quality Assurance support in New Product Introduction (NPI) team
+ Coach site Quality Assurance professionals on resolution of complex problems
+ Participate in regulatory inspections, and interact directly with regulatory inspectors
+ Supporting other Quality Assurance initiatives/activities such as continuous improvement projects, supplier quality, stability program, product quality review, customer complaint investigation.
**Win**
**What we expect of you**
**Basic Qualifications**
+ Doctorate degree OR
+ Master's degree and 2 years of directly related experience OR
+ Bachelor's degree and 4 years of directly related experience OR
+ Diploma and 8 years of directly related experience
+ 8 years related work experience (manufacturing, process development, or quality assurance) in the pharmaceutical / biologics industry with progressively increasing responsibility and demonstrated experience in project management, quality assurance, and quality systems.
+ Direct experience with bulk manufacturing of biopharmaceuticals/API preferred.
+ Demonstrated proficiency of written and verbal communication skills (including technical writing and presentations) with ability to communicate and collaborate effectively with technical and senior management staff.
+ Experience with regulatory audits and inspections
+ Problem solving skills with the ability to apply logic and assess data to reach decisions and solutions related to compliance and product quality.
**Thrive**
**What you can expect of us**
As we work to develop treatments that take care of others, so we work to care for our teammates' professional and personal growth and well-being.
+ Vast opportunities to learn and move up and across our global organization
+ Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
+ Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
**Your selection for this role will be subject to fulfilling the medical requirements of this job scope. If so, you will be informed of the medical check(s) that you may need to undergo. All medical related expenses incurred from this medical check shall be borne by the company.**
**Apply now**
**for a career that defies imagination**
In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.
**careers.amgen.com**
**Equal Opportunity Statement**
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.
**Amgen Singapore Manufacturing**
**HOW MIGHT YOU DEFY IMAGINATION?**
Amgen is one of the world's leading independent biotechnology companies. For over 4 decades, Amgen has pioneered biotechnology breakthroughs, to bring state-of-the-art medicines from laboratory to the patient. Amgen has not only discovered and developed innovative human therapeutics but has invested in cutting edge manufacturing capability and support services to deliver these exciting therapies to medical teams around the world. Japan and Asia Pacific (JAPAC) is the fastest growing region in Amgen. Now we are hiring a **Specialist Quality Assurance** in **Amgen Singapore Manufacturing.**
**Live**
**What you will do**
Responsible for providing oversight and leadership for quality systems execution and operations support, the Specialist Quality Assurance will support manufacturing operations and IPC testing through presence on the floor, and support of complex manufacturing investigations, change control, and unexpected result investigations.
Main Responsibilities:
+ Provide Quality oversight to plant operations, ensuring appropriate application and execution of GMP compliance requirements and Amgen Quality Management System in plant operations through phases of commissioning, process qualification, regulatory approval and market supply
+ Support routine GMP documentation review activities (e.g. electronic batch records, SOPs, logbooks, work orders, batch production reports and validation protocols etc.) and ensure key performance indicator met targeted metrics
+ Co-lead and support the deployment of Amgen quality systems, including management review, validation, change control and CAPA and ensure that the systems are managed in compliance with cGMP expectations
+ Participate in complex root cause investigations for deviations
+ Review and approve deviation investigations, change controls, and other quality records (with focus on highly complex records)
+ Provides Quality Assurance support in New Product Introduction (NPI) team
+ Coach site Quality Assurance professionals on resolution of complex problems
+ Participate in regulatory inspections, and interact directly with regulatory inspectors
+ Supporting other Quality Assurance initiatives/activities such as continuous improvement projects, supplier quality, stability program, product quality review, customer complaint investigation.
**Win**
**What we expect of you**
**Basic Qualifications**
+ Doctorate degree OR
+ Master's degree and 2 years of directly related experience OR
+ Bachelor's degree and 4 years of directly related experience OR
+ Diploma and 8 years of directly related experience
+ 8 years related work experience (manufacturing, process development, or quality assurance) in the pharmaceutical / biologics industry with progressively increasing responsibility and demonstrated experience in project management, quality assurance, and quality systems.
+ Direct experience with bulk manufacturing of biopharmaceuticals/API preferred.
+ Demonstrated proficiency of written and verbal communication skills (including technical writing and presentations) with ability to communicate and collaborate effectively with technical and senior management staff.
+ Experience with regulatory audits and inspections
+ Problem solving skills with the ability to apply logic and assess data to reach decisions and solutions related to compliance and product quality.
**Thrive**
**What you can expect of us**
As we work to develop treatments that take care of others, so we work to care for our teammates' professional and personal growth and well-being.
+ Vast opportunities to learn and move up and across our global organization
+ Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
+ Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
**Your selection for this role will be subject to fulfilling the medical requirements of this job scope. If so, you will be informed of the medical check(s) that you may need to undergo. All medical related expenses incurred from this medical check shall be borne by the company.**
**Apply now**
**for a career that defies imagination**
In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.
**careers.amgen.com**
**Equal Opportunity Statement**
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.
Is this job a match or a miss?
Apply Now
0
Job Description
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
**The Position**
Reporting to the Head of QC Support Operation, support projects within QC functions for QC equipments and master data maintenace of Laboratory Execution system within schedule and
according to the company policy.
**Key Responsibilities:**
+ As part of the QC Support Operations Team to provide support for routine QC activities including:
- Purchasing, qualification/re-qualification of laboratory equipment and computer systems
- All other tactical support activities required to support the business needs
+ Execute projects which encompass QC equipment qualification related activities following cGMP requirements.
+ Perform data documentation for executed projects following cGMP procedures.
+ Support routine management of equipment and reagent master data in Laboratory Execution Systems (LES)
+ Perform development, verification and deployment of LES recipes or other QC systems
+ Ensure that data, documentation and laboratory processes are in a constant state of regulatory compliance and inspection readiness.
+ Timely resolution of issues, including raising discrepancies, investigations and implementation of CAPAs.
**Education:**
+ Degree in Chemistry, Microbiology, Biochemistry, Life Science or equivalent
**Experience:**
+ 0 - 3 years of related working experience for degree holders or equivalent holders with combination of education and relative work experience is preferred
**Knowledge/Skills/Competencies:**
+ Strong problem solving capability. Able to determine when to escalate issue.
+ Ability to organize and plan effectively. Effective resource management.
+ Demonstrate good verbal and written communication skills in English.
**Who we are**
A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let's build a healthier future, together.
**Roche is an Equal Opportunity Employer.**
**The Position**
Reporting to the Head of QC Support Operation, support projects within QC functions for QC equipments and master data maintenace of Laboratory Execution system within schedule and
according to the company policy.
**Key Responsibilities:**
+ As part of the QC Support Operations Team to provide support for routine QC activities including:
- Purchasing, qualification/re-qualification of laboratory equipment and computer systems
- All other tactical support activities required to support the business needs
+ Execute projects which encompass QC equipment qualification related activities following cGMP requirements.
+ Perform data documentation for executed projects following cGMP procedures.
+ Support routine management of equipment and reagent master data in Laboratory Execution Systems (LES)
+ Perform development, verification and deployment of LES recipes or other QC systems
+ Ensure that data, documentation and laboratory processes are in a constant state of regulatory compliance and inspection readiness.
+ Timely resolution of issues, including raising discrepancies, investigations and implementation of CAPAs.
**Education:**
+ Degree in Chemistry, Microbiology, Biochemistry, Life Science or equivalent
**Experience:**
+ 0 - 3 years of related working experience for degree holders or equivalent holders with combination of education and relative work experience is preferred
**Knowledge/Skills/Competencies:**
+ Strong problem solving capability. Able to determine when to escalate issue.
+ Ability to organize and plan effectively. Effective resource management.
+ Demonstrate good verbal and written communication skills in English.
**Who we are**
A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let's build a healthier future, together.
**Roche is an Equal Opportunity Employer.**
Is this job a match or a miss?
Apply Now
1
Job Description
**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.
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.
Is this job a match or a miss?
Apply Now
2
Job Description
**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.
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.
Is this job a match or a miss?
Apply Now
3
QC Specialist II x 12 hours rotating shift ie 8am to 8pm and 8pm to 8am
Singapore
Danaher Corporation
Posted 19 days ago
Job Viewed
Job Description
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Pall Corporation, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
As a global leader in high-tech filtration, separation, and purification, Pall Corporation thrives on helping our customers solve their toughest challenges. Our products serve diverse, global customer needs across a wide range of applications to advance health, safety and environmentally responsible technologies. From airplane engines to hydraulic systems, scotch to smartphones, OLED screens to paper-everyday Pall is there, helping protect critical operating assets, improve product quality, minimize emissions and waste, and safeguard health. For the exponentially curious, Pall is a place where you can thrive and amplify your impact on the world. Find what drives you on a team with a more than 75-year history of discovery, determination, and innovation.
Learn about the Danaher Business System which makes everything possible.
The QC Specialist is responsible for executing testing, sampling and inspection procedures on raw materials, equipment, in-process materials, and/or finished products to ensure that product specifications and company and regulatory requirements are met.
This position is part of the Quality Control Department reporting to the QC Manager and will be located in Benoi, Singapore.
In this role, you will have the opportunity to:
+ Support IQ, OQ, and PQ activities, instrument calibration, and laboratory equipment setup
+ Perform QC testing and inspections, including sample preparation, go/no‑go decisions, and escalation of failed or high‑risk results
+ Investigate non‑conformances and support continuous improvement initiatives such as PSP, 5S, ESH, and Kaizen
The essential requirements of the job include:
+ Education & experience: Degree in a relevant scientific discipline with preferably a minimum of 3 years' hands‑on experience in routine QC laboratory operations.
+ Operational & compliance capability: Data entry and basic data analysis (Excel/Word), able to support production output, quality escalation, rotating shift work, and perform physical tasks (up to 20 kg) in a controlled white‑room environment.
+ Technical advantage: Prior exposure to ICP‑MS, GC‑MS, Liquid Particle Counter (LPC), and TOC, with solid understanding of GMP, GDP, GLP, and application of quality and specification criteria in QC testing
It would be a plus if you also possess previous experience in:
+ Familiarity on Microsoft software and SAP/other ERP experience (specifically in manufacturing environment or cleanroom environment)
Pall Corporation, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
#LI-onsite #LI-VH1
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Pall Corporation, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
As a global leader in high-tech filtration, separation, and purification, Pall Corporation thrives on helping our customers solve their toughest challenges. Our products serve diverse, global customer needs across a wide range of applications to advance health, safety and environmentally responsible technologies. From airplane engines to hydraulic systems, scotch to smartphones, OLED screens to paper-everyday Pall is there, helping protect critical operating assets, improve product quality, minimize emissions and waste, and safeguard health. For the exponentially curious, Pall is a place where you can thrive and amplify your impact on the world. Find what drives you on a team with a more than 75-year history of discovery, determination, and innovation.
Learn about the Danaher Business System which makes everything possible.
The QC Specialist is responsible for executing testing, sampling and inspection procedures on raw materials, equipment, in-process materials, and/or finished products to ensure that product specifications and company and regulatory requirements are met.
This position is part of the Quality Control Department reporting to the QC Manager and will be located in Benoi, Singapore.
In this role, you will have the opportunity to:
+ Support IQ, OQ, and PQ activities, instrument calibration, and laboratory equipment setup
+ Perform QC testing and inspections, including sample preparation, go/no‑go decisions, and escalation of failed or high‑risk results
+ Investigate non‑conformances and support continuous improvement initiatives such as PSP, 5S, ESH, and Kaizen
The essential requirements of the job include:
+ Education & experience: Degree in a relevant scientific discipline with preferably a minimum of 3 years' hands‑on experience in routine QC laboratory operations.
+ Operational & compliance capability: Data entry and basic data analysis (Excel/Word), able to support production output, quality escalation, rotating shift work, and perform physical tasks (up to 20 kg) in a controlled white‑room environment.
+ Technical advantage: Prior exposure to ICP‑MS, GC‑MS, Liquid Particle Counter (LPC), and TOC, with solid understanding of GMP, GDP, GLP, and application of quality and specification criteria in QC testing
It would be a plus if you also possess previous experience in:
+ Familiarity on Microsoft software and SAP/other ERP experience (specifically in manufacturing environment or cleanroom environment)
Pall Corporation, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
#LI-onsite #LI-VH1
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
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4
Job Description
**Specialist Quality Assurance**
**Amgen Singapore Manufacturing**
**HOW MIGHT YOU DEFY IMAGINATION?**
Amgen is one of the world's leading independent biotechnology companies. For over 4 decades, Amgen has pioneered biotechnology breakthroughs, to bring state-of-the-art medicines from laboratory to the patient. Amgen has not only discovered and developed innovative human therapeutics but has invested in cutting edge manufacturing capability and support services to deliver these exciting therapies to medical teams around the world. Japan and Asia Pacific (JAPAC) is the fastest growing region in Amgen. Now we are hiring a **Specialist Quality Assurance** in **Amgen Singapore Manufacturing.**
**Live**
**What you will do**
Responsible for providing oversight and leadership for quality systems execution and operations support, the Specialist Quality Assurance will support manufacturing operations and IPC testing through presence on the floor, and support of complex manufacturing investigations, change control, and unexpected result investigations.
Main Responsibilities:
+ Provide Quality oversight to plant operations, ensuring appropriate application and execution of GMP compliance requirements and Amgen Quality Management System in plant operations through phases of commissioning, process qualification, regulatory approval and market supply
+ Support routine GMP documentation review activities (e.g. electronic batch records, SOPs, logbooks, work orders, batch production reports and validation protocols etc.) and ensure key performance indicator met targeted metrics
+ Co-lead and support the deployment of Amgen quality systems, including management review, validation, change control and CAPA and ensure that the systems are managed in compliance with cGMP expectations
+ Participate in complex root cause investigations for deviations
+ Review and approve deviation investigations, change controls, and other quality records (with focus on highly complex records)
+ Provides Quality Assurance support in New Product Introduction (NPI) team
+ Coach site Quality Assurance professionals on resolution of complex problems
+ Participate in regulatory inspections, and interact directly with regulatory inspectors
+ Supporting other Quality Assurance initiatives/activities such as continuous improvement projects, supplier quality, stability program, product quality review, customer complaint investigation.
**Win**
**What we expect of you**
**Basic Qualifications**
+ Doctorate degree OR
+ Master's degree and 2 years of directly related experience OR
+ Bachelor's degree and 4 years of directly related experience OR
+ Diploma and 8 years of directly related experience
+ 8 years related work experience (manufacturing, process development, or quality assurance) in the pharmaceutical / biologics industry with progressively increasing responsibility and demonstrated experience in project management, quality assurance, and quality systems.
+ Direct experience with bulk manufacturing of biopharmaceuticals/API preferred.
+ Demonstrated proficiency of written and verbal communication skills (including technical writing and presentations) with ability to communicate and collaborate effectively with technical and senior management staff.
+ Experience with regulatory audits and inspections
+ Problem solving skills with the ability to apply logic and assess data to reach decisions and solutions related to compliance and product quality.
**Thrive**
**What you can expect of us**
As we work to develop treatments that take care of others, so we work to care for our teammates' professional and personal growth and well-being.
+ Vast opportunities to learn and move up and across our global organization
+ Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
+ Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
**Your selection for this role will be subject to fulfilling the medical requirements of this job scope. If so, you will be informed of the medical check(s) that you may need to undergo. All medical related expenses incurred from this medical check shall be borne by the company.**
**Apply now**
**for a career that defies imagination**
In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.
**careers.amgen.com**
**Equal Opportunity Statement**
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.
**Amgen Singapore Manufacturing**
**HOW MIGHT YOU DEFY IMAGINATION?**
Amgen is one of the world's leading independent biotechnology companies. For over 4 decades, Amgen has pioneered biotechnology breakthroughs, to bring state-of-the-art medicines from laboratory to the patient. Amgen has not only discovered and developed innovative human therapeutics but has invested in cutting edge manufacturing capability and support services to deliver these exciting therapies to medical teams around the world. Japan and Asia Pacific (JAPAC) is the fastest growing region in Amgen. Now we are hiring a **Specialist Quality Assurance** in **Amgen Singapore Manufacturing.**
**Live**
**What you will do**
Responsible for providing oversight and leadership for quality systems execution and operations support, the Specialist Quality Assurance will support manufacturing operations and IPC testing through presence on the floor, and support of complex manufacturing investigations, change control, and unexpected result investigations.
Main Responsibilities:
+ Provide Quality oversight to plant operations, ensuring appropriate application and execution of GMP compliance requirements and Amgen Quality Management System in plant operations through phases of commissioning, process qualification, regulatory approval and market supply
+ Support routine GMP documentation review activities (e.g. electronic batch records, SOPs, logbooks, work orders, batch production reports and validation protocols etc.) and ensure key performance indicator met targeted metrics
+ Co-lead and support the deployment of Amgen quality systems, including management review, validation, change control and CAPA and ensure that the systems are managed in compliance with cGMP expectations
+ Participate in complex root cause investigations for deviations
+ Review and approve deviation investigations, change controls, and other quality records (with focus on highly complex records)
+ Provides Quality Assurance support in New Product Introduction (NPI) team
+ Coach site Quality Assurance professionals on resolution of complex problems
+ Participate in regulatory inspections, and interact directly with regulatory inspectors
+ Supporting other Quality Assurance initiatives/activities such as continuous improvement projects, supplier quality, stability program, product quality review, customer complaint investigation.
**Win**
**What we expect of you**
**Basic Qualifications**
+ Doctorate degree OR
+ Master's degree and 2 years of directly related experience OR
+ Bachelor's degree and 4 years of directly related experience OR
+ Diploma and 8 years of directly related experience
+ 8 years related work experience (manufacturing, process development, or quality assurance) in the pharmaceutical / biologics industry with progressively increasing responsibility and demonstrated experience in project management, quality assurance, and quality systems.
+ Direct experience with bulk manufacturing of biopharmaceuticals/API preferred.
+ Demonstrated proficiency of written and verbal communication skills (including technical writing and presentations) with ability to communicate and collaborate effectively with technical and senior management staff.
+ Experience with regulatory audits and inspections
+ Problem solving skills with the ability to apply logic and assess data to reach decisions and solutions related to compliance and product quality.
**Thrive**
**What you can expect of us**
As we work to develop treatments that take care of others, so we work to care for our teammates' professional and personal growth and well-being.
+ Vast opportunities to learn and move up and across our global organization
+ Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
+ Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits
**Your selection for this role will be subject to fulfilling the medical requirements of this job scope. If so, you will be informed of the medical check(s) that you may need to undergo. All medical related expenses incurred from this medical check shall be borne by the company.**
**Apply now**
**for a career that defies imagination**
In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.
**careers.amgen.com**
**Equal Opportunity Statement**
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.
Is this job a match or a miss?
Apply Now
5
Microbiologist (QC Analyst/ Pharma/ Contract)
Posted 6 days ago
Job Viewed
Job Description
Microbiologist (QC Analyst/ Pharma/ Contract)
12 Months Contract
Location : Gul Circle (5 mins walk from MRT)
Basic Salary : Up to $5,500 depending on experience
Industry : Pharmaceutical
Responsibilities
- Executing analytical testing in a timely manner, ensuring adherence to the committed scheduled plans
- Performing his/ her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records, related to these tasks
- Recording all expected raw data, calculations, information, related to his/her tasks, to comply with cGMP and data integrity requirements
- Ensuring that is trained and qualified to the assigned analytical testing that requires to be qualified
- Performing the QC data review of executed tests by other analysts in a timely manner, ensuring adherence to the committed scheduled plans
- Informing his/her manager of any quality or HSE event (deviations, OOx,…) in a timely manner to ensure investigation and impact assessment are performed appropriately
- Participating actively to any investigation, where is involved, to ensure investigations and impact assessment are performed appropriately
- Executing assigned CAPAs related to remediation plans, continuous improvements
- Ensuring that his/her lab/facilities, lab instruments are kept in a quality and safety status to ensure that they can be used appropriately.
- Owning assigned stability studies, in compliance with approved stability program
- Ensuring the issuance and review of all deliverables related to assigned stability studies, such as risk assessment, protocols, reports, data trending, deviations, and summary reports
- Ensuring that sampling and testing related to stability is executed in a timely manner and stability results trend performed on time, including reports issuance
- Ensuring that all expected stability data (including events, change control…) are compiled in a proper way, to provide appropriate data trending and statistical analysis of stability studies, in compliance with associated stability protocols
Additional Accountabilities
- Review analytical results and perform audit trail review before batch release.
- Carry out on-the-job training for General and Specific Analytical Method to QC analysts and chemical technicians, by incorporating cGMP and safety aspects of the procedures.
- Perform troubleshooting of equipment in the laboratory and provide guidance to QC analysts on the troubleshooting.
- Trained and work independently on specific testing method
- Ensure availability of workplace risk assessment and safe working procedures for contractors and the quality personnel. Ensure safe working in all areas of work by practicing and communicating safety message at +QDCI Sanofi Manufacturing System (SMS) Awareness, Life Saving Rules (LSR), GMP/Data Integrity Awareness
- Other responsibilities that are not included in the above are related to quality assignments.
Lim Pey Chyi (Apple) -
Recruitment Consultant (R )
Manpower Staffing Services (S) Pte Ltd
EA Licence: 02C3423
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Apply Now
6
Quality Executive (Training Provided / QA Analyst / Quality Assurance & Control)
Remote
SGD4,000 Monthly
EA RECRUITMENT PTE. LTD.
Posted 6 days ago
Job Viewed
Job Description
MNC Company
Basic $3500 - $4000 + AWS + Variable Bonus
Excellent Welfare and Benefits + Career progression
Working location: Aljunied
Working hours: Monday to Friday (9am to 6pm)
Job Responsibilities:
Develops, implements, supports and/or leads process improvement efforts, quality initiatives, cross-functional efforts and sustainable corrective measures.
Plans, facilitates or executes internal, customer, supplier or certification audits. Ensures corrective actions specific to non-conformance and audit results are appropriately robust and sustainable to maintain certifications.
Collects and analyzes data obtained from internal quality audits, customer and supplier feedback, and process evaluations to identify opportunities to improve processes and procedures and ensure quality goals are achieved.
Works closely and maintains good working relationship with internal department representatives, customers, suppliers, and/or external certification/regulatory representatives.
Trains employees in continuous improvement techniques and the quality management system.
Other duties as assigned.
Job Requirements:
Possess minimum Bachelor’s Degree qualification or equivalent.
Training will be provided for those lesser/without experience.
Candidates are encouraged to apply this position via Apply Now button with the following information in the resume
Work experiences and job responsibilities
Current and Expected salary
Reason for leaving
Date of availability
Education background
We regret that only shortlisted candidates will be contacted.
LIONG ZHAO GUAN (R )
EA Recruitment Pte Ltd
EA License No: 21C0492
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7
QC Validation Specialist (Equipment Qualification/ Pharma/ Contract)
Posted 6 days ago
Job Viewed
Job Description
QC Validation Specialist (Equipment Qualification/ Pharma/ Contract)
Duration: 6 months
Location: Tuas
Salary : Up to $10,000 depending on experience
Our client is a US healthcare and a leading global biopharmaceutical company. They have more than 69,000 employees across 140 countries with a heritage of more than 125 years. Our client is committed to provide patients and customers with a reliable supply of high-quality, safe, and effective medicines and vaccines. Their global supply strategy relies on manufacturing capabilities and expertise to achieve this mission
Responsibilities
- Perform/review system qualification, requalification, relocation, decommissioning and retirement for laboratory equipment in accordance with approved procedures and standard lead time.
- Assume role of Subject-Matter-Expert of laboratory system lifecycle, collaborates closely with cross-functional teams and above-site functions. This includes initiating alignments proactively, sharing expertise, and providing input to ensure alignment and consistency across the organization.
- Author/review Quality Notifications and Test Exception Reports, lead root cause analysis and ensure effective implementation of related actions within the agreed timeframe.
- Conduct troubleshooting of laboratory system lifecycle, identifying and resolving any issues that may impact the business/work efficiency and compliance.
- Identify opportunities and propose solutions to improve efficiency and compliance in processes, standards, and best practices within the team.
- Provide leadership, expert guidance and support to team members, acting as a go-to resource for problem-solving and decision-making.
- Provide skills training to other team members, ensuring they have the necessary knowledge and competencies to perform their duties effectively.
- Any other duties as assigned by reporting manager.
Requirements:
- Diploma or bachelor’s degree in chemical engineering or any other relevant engineering field
- At least 5 years of experience in qualification, requalification, relocation, decommissioning and retirement of Good Manufacturing Practice (GMP) Lab equipment (not limited to Ultraviolet–Visible (UV-Vis) Spectrometer, Total Organic Carbon (TOC) Analyzer, Microplate Reader, Liquid Particle Counter, Capillary Electrophoresis (CE), High-Performance Liquid Chromatography (HPLC), Analytical Balances, Incubators, Particle Counters)
- Experience in GMP environment within the pharmaceutical/chemical manufacturing.
Lim Pey Chyi –
Recruitment Consultant (R )
Manpower Staffing Services (S) Pte Ltd
EA Licence: 02C3423
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8
Job Description
About No deviation
At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation.
We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development – empowering our team members to grow personally and professionally.
Position Overview
The QC Personnel will be responsible for supporting day-to-day Quality Control laboratory activities, including testing, documentation, method validation support, data review, and compliance with GMP requirements. The role requires hands-on experience with laboratory systems such as GLIMS , Veeva , and SAP , as well as experience in analytical method validation activities.
Key Responsibilities
- Perform routine QC testing for raw materials, intermediates, finished products, stability samples, and/or environmental monitoring samples, as applicable
- Execute laboratory testing in accordance with approved SOPs, test methods, specifications, and GMP requirements.
- Ensure all laboratory activities are completed accurately, timely, and in compliance with data integrity expectations.
- Support sample receipt, testing coordination, result entry, and laboratory documentation.
- Support analytical method validation, verification, transfer, and qualification activities.
- Execute validation protocols and document results in accordance with approved acceptance criteria.
- Assist in the preparation, review, and closure of method validation protocols, reports, deviations, and supporting documentation.
- Support troubleshooting of analytical methods and laboratory investigations where required.
- Use GLIMS for sample management, test assignment, result entry, and laboratory workflow tracking.
- Use Veeva for document management, SOP retrieval, document review, training, and quality records where applicable.
- Use SAP for material/sample-related transactions, inventory checks, batch information retrieval, or quality-related processes.
- Ensure proper documentation practices in line with ALCOA+ principles and GMP expectations.
- Support laboratory investigations, OOS/OOT investigations, deviations, CAPA, and change control activities.
- Ensure timely escalation of abnormal results, laboratory issues, equipment issues, or documentation discrepancies.
- Participate in internal audits, external inspections, and laboratory readiness activities.
- Maintain laboratory areas, equipment, reagents, standards, and records in an inspection-ready state
- Support calibration, maintenance, and qualification readiness of laboratory equipment.
- Assist in laboratory process improvements, system updates, and workflow optimization.
- Work closely with QA, Manufacturing, MSAT, Validation, and Supply Chain teams to support product release and compliance requirements.
Required Qualifications
- Diploma or Degree in Chemistry, Pharmaceutical Science, Biotechnology, Microbiology, Life Sciences, or related discipline .
- Minimum 2 to 5 years of QC laboratory experience in a pharmaceutical, biologics, medical device, or GMP-regulated environment.
- Experience with method validation, method verification, or method transfer is required.
- Hands-on experience with laboratory or quality systems such as GLIMS, Veeva, and SAP .
- Experience in QC testing, laboratory documentation, investigations, and GMP compliance.
- Familiar with GMP, GDP, data integrity, ALCOA+, and laboratory compliance requirements.
- Experience with analytical techniques such as HPLC, GC, UV, pH, conductivity, TOC, endotoxin, bioburden, sterility, or other QC methods will be advantageous.
- Able to execute and document method validation activities according to approved protocols.
- Comfortable working with electronic systems for sample tracking, document control, training, and material/batch-related transactions.
Why join us?
- Generous Leave Policy.
- Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
- Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company.
- Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated.
- Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.
How to apply
Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team!
Please submit your resume, outlining your qualifications and experience relevant to the role, here.
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9