136 Pharmaceutical Analysis jobs in Singapore

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies believes that it is a global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 35 years, Eurofins has grown from one laboratory in Nantes, France to ca. 62,000 staff across a decentralised and entrepreneurial network of over 900 laboratories in 62 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2024, Eurofins generated total revenues of EUR 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

Essential Duties and Responsibilities:

• Demonstrates and promotes the company vision
• Regular attendance and punctuality
• Applies GMP/GLP in all areas of responsibility, as appropriate
• Learns to conduct routine analyses in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines.
• Learns how to document work and maintain study documentation and laboratory records.
• Learns how to use laboratory equipment and software appropriate for assigned tasks.
• Attends and participates in project meetings.
• Learns to perform peer review of data.
• Learns to plan assigned workload on a daily basis and effectively schedule multiple assignments.
• Contributes to a cohesive team environment. Plans individual workload in coordination with team members.
• Maintains a clean and safe laboratory work environment.
• Conducts all activities in a safe and efficient manner
• Performs other duties as assigned

Qualifications

Job Requirement:

• Candidate must possess at least Diploma in Chemistry, Food Science or equivalent
• Interacts with operational personnel, scientific personnel, and department management
• May work with potentially hazardous materials
• Will be exposed to potential food allergens (ex. Milk, tree nuts, peanuts, fish, shellfish, etc.)
• Overtime and weekend work as required
• Work requires some standing and sitting for long periods of time, including working within a laboratory hood and standing at a bench top
• Work requires use of PPE (personal protective equipment)
• Will be exposed to potential food allergens

Additional Information

What we offer: As an employer, we’re keen to look after our people with as much dedication as they look after our patients. That’s why we offer competitive salaries, excellent training and exceptional career prospects. We’re a growing and ambitious company, so there is huge potential here to develop with us and enjoy fantastic rewards in your career.

Your data:
As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations.

Eurofins Food Testing is an Equal Opportunities Company.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies believes that it is a global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 35 years, Eurofins has grown from one laboratory in Nantes, France to ca. 62,000 staff across a decentralised and entrepreneurial network of over 900 laboratories in 62 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
In 2024, Eurofins generated total revenues of EUR 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description
Essential Duties and Responsibilities:
Demonstrates and promotes the company vision
Regular attendance and punctuality
Applies GMP/GLP in all areas of responsibility, as appropriate
Learns to conduct routine analyses in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines.
Learns how to document work and maintain study documentation and laboratory records.
Learns how to use laboratory equipment and software appropriate for assigned tasks.
Attends and participates in project meetings.
Learns to perform peer review of data.
Learns to plan assigned workload on a daily basis and effectively schedule multiple assignments.
Contributes to a cohesive team environment. Plans individual workload in coordination with team members.
Maintains a clean and safe laboratory work environment.
Conducts all activities in a safe and efficient manner
Performs other duties as assigned
Qualifications
Job Requirement:
Candidate must possess at least Diploma in Chemistry, Food Science or equivalent
Interacts with operational personnel, scientific personnel, and department management
May work with potentially hazardous materials
Will be exposed to potential food allergens (ex. Milk, tree nuts, peanuts, fish, shellfish, etc.)
Overtime and weekend work as required
Work requires some standing and sitting for long periods of time, including working within a laboratory hood and standing at a bench top
Work requires use of PPE (personal protective equipment)
Will be exposed to potential food allergens
Additional Information
What we offer: As an employer, we’re keen to look after our people with as much dedication as they look after our patients. That’s why we offer competitive salaries, excellent training and exceptional career prospects. We’re a growing and ambitious company, so there is huge potential here to develop with us and enjoy fantastic rewards in your career.
Your data:
As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations.
Eurofins Food Testing is an Equal Opportunities Company.
#J-18808-Ljbffr

Essential Duties and Responsibilities:

• Demonstrates and promotes the company vision
• Regular attendance and punctuality
• Applies GMP/GLP in all areas of responsibility, as appropriate
• Learns to conduct routine analyses in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines
• Learns how to document work and maintain study documentation and laboratory records
• Learns how to use laboratory equipment and software appropriate for assigned tasks
• Attends and participates in project meetings
• Learns to perform peer review of data
• Learns to plan assigned workload on a daily basis and effectively schedule multiple assignments
• Contributes to a cohesive team environment
• Plans individual workload in coordination with team members
• Maintains a clean and safe laboratory work environment
• Conducts all activities in a safe and efficient manner
• Performs other duties as assigned

Job Requirement:

• Candidate must possess at least Diploma in Food Science, Chemistry, Science or equivalent
• Interacts with operational personnel, scientific personnel, and department management
• May work with potentially hazardous materials
• Overtime and weekend work as required
• Work requires some standing and sitting for long periods of time, including working within a laboratory hood and standing at a bench top
• Work requires use of PPE (personal protective equipment)
• Will be exposed to potential food allergens
• Entry level are welcome

Essential Duties and Responsibilities:

• Demonstrates and promotes the company vision
• Regular attendance and punctuality
• Applies GMP/GLP in all areas of responsibility, as appropriate
• Learns to conduct routine analyses in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines
• Learns how to document work and maintain study documentation and laboratory records
• Learns how to use laboratory equipment and software appropriate for assigned tasks
• Attends and participates in project meetings
• Learns to perform peer review of data
• Learns to plan assigned workload on a daily basis and effectively schedule multiple assignments
• Contributes to a cohesive team environment
• Plans individual workload in coordination with team members
• Maintains a clean and safe laboratory work environment
• Conducts all activities in a safe and efficient manner
• Performs other duties as assigned

Job Requirement:

• Candidate must possess at least Diploma in Food Science, Chemistry, Science or equivalent
• Interacts with operational personnel, scientific personnel, and department management
• May work with potentially hazardous materials
• Overtime and weekend work as required
• Work requires some standing and sitting for long periods of time, including working within a laboratory hood and standing at a bench top
• Work requires use of PPE (personal protective equipment)
• Will be exposed to potential food allergens
• Entry level are welcome

about the company
Join a leader in the captivating world of fragrances. They are a well-established company with a rich heritage and a passion for crafting the scents that define brands and create memories. With a strong presence across Asia, Europe, and the Americas, you will be part of a dynamic and multicultural team driving innovation in the fragrance industry.

about the job

• Analyze and deconstruct complex fragrances from a wide range of market products across all categories.
• Employ advanced analytical techniques (GC/MS, FID) to reverse-engineer and reconstitute complete fragrance formulas.
• Lead analytical projects with a high degree of autonomy, from conception through to final reporting.
• Provide critical analytical insights and expert findings to guide the creative teams.
• Maintain state-of-the-art laboratory equipment and act as the subject matter expert for all fragrance raw materials.

about the manager/team
You will be a senior member of our collaborative team in Singapore, working closely with creative Perfumers. Reporting to the Manager, you'll be relied upon for your technical expertise and leadership. A significant part of your role will be mentoring junior analyst and elevating the team's technical capabilities.

skills and experience required

• Bachelor Degree in Chemistry or a related scientific field.
• Minimum 5 years of experience as a Fragrance Analyst or Analytical Chemist in the fragrance industry.
• Proficiency with GC/MS, FID, and related data analysis software (e.g., ChemStation).
• Proven success in fragrance reverse-engineering and formula reconstitution.
• Deep knowledge of synthetic and natural perfumery raw materials.

To apply online please use the 'apply' function and upload your updated resume, alternatively you may contact Florence Pang at

(EA: 94C3609/ R25139901)

Job Description

This is job position is a chemist who will lead the analytical activities in our state-of-the-art analytical laboratory. The successful candidate will be responsible for overseeing daily operations, ensuring data integrity, maintaining instrumentation, and driving analytical excellence across a range of techniques including HPLC, FTIR, DSC, TGA, biocompatibility testing and more.

Key Responsibilities

• Lead all analytical activities within the Characterization Laboratory, including operating, maintaining, and troubleshooting advanced instrumentation including HPLC, FTIR, DSC, TGA, biocompatibility testing, and additional analytical tools as required
• Develop, validate, and implement new analytical methods according to product development requirement and in compliance with regulatory standards
• Interpret and report analytical data with accuracy and clarity
• Create and maintain documentation including testing reports, and work instruction procedures for laboratory equipment
• Ensure on time validation and calibration of various instruments
• Ensure laboratory compliance with safety, quality, and documentation protocols
• Collaborate with Technology, QC, and production teams to support product development and quality assurance
• Manage inventory of reagents, consumables, and calibration standards
• Train and mentor technicians in daily routine work

Qualifications

• Bachelor’s degree in chemistry, analytical chemistry, or related field with minimum 2 years of hands-on experience in an analytical laboratory setting.
• Open for Diploma holder with minimum 5 years of hands-on experience
• Proven expertise in operating and maintaining analytical instruments
• Understanding of method development and validation protocols
• Effective communication skills with all levels of employment both verbally and in writing

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.

About the role:

This position is required perform all tasks associated with the QC analytical lab operations which include chemical analysis, biochemical analysis, equipment calibration/maintenance, records review, records approval, deviation/investigation write up/review, equipment qualification, method validation, method transfer and other tasks as assigned.

How you will contribute:

Core Responsibilities:

• Perform chemistry, biochemistry analysis of in-process samples, bulk drug substance (BDS), non-routine samples.

• Ensure tests assigned are performed in a timely manner in compliance to Standard Operating procedures

• Perform equipment calibration and maintenance.

• Perform review/approval of QC records/ log books.

• Perform trending of lab results.

• Initiate, participate and complete in Out Of Specification (OOS), Invalid test and Lab Deviation Investigation/ Write-Up and assist in timely closure of laboratory invalid results, lab investigation and CAPA with minimum guidance

• Write/revise SOPs, forms, training qualifications (TQ) and risk assessments (RA).

• Act as a Subject Matter Expert (SME) to provide technical advice to QC Personnel in laboratory related troubleshooting, e.g. lab equipment failure, method

• Provide appropriate training for the QC Analytical Team.

• Participate in method validation/ transfer or equipment qualification when necessary

• Ensure proper, safe handling and disposal of wastes; ensuring a safe working environment

General Responsibilities:

• Carry out 5S and ensures good housekeeping of Analytical Lab area.

• Support and participates in Operation Excellence initiatives (such as GEMBA and GMP walk).

• Lead in cross functional investigation.

• Coach and mentor junior Chemist.

• Participate in projects towards improving safety performance and continuous improvement initiatives

• Demonstrate strong technical knowledge and associated regulatory expectation.

• QC Chemist may cover for another QC Chemist of similar functions/areas in his/her absence by signing documents on his/her behalf.

• Assist Supervisor to support internal and external compliance audits.

• Responsibility to adhere to any applicable EHS requirements.

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

• Any other duties as assigned by supervisor

What you bring to Takeda:

Education and Experience Requirements

• The candidate should have at least a Degree in pharmaceutical sciences, life sciences, biology, biotechnology chemistry, chemical engineering, or a related discipline.

• Certification and trainings such as auditor training or QP training will be advantageous.

• A minimum experience of 10 years, with 5 years of supervisory position, in the pharmaceutical or biotechnology in quality assurance, GMP compliance, operations or validation, ideally in a multinational company.

• FDA/EU cGMP know-how and a thorough understanding of ICH guidelines, together with exposure to the international regulatory network.

• Able to logically solve problems in order to find timely solutions.

• An ability to interact and communicate with all types of personalities in an effective and diplomatic manner

• Good decision-making capability

Key Skills and Competencies

• Project Management Skills

o Organization and planning skills

o Analytical and Logical thinking skills

o Ability to work and collaborate within the team and with cross departments

• Technical Skills

o Has substantial knowledge and understanding in terms of regulatory standards requirements e.g. USP, EP, 21CFR, ICH etc.

o Knowledge in Ion Chromatography (IC), High Performance Liquid Chromatography (HPLC), Fluorescence spectrometer (FLS), pH, Conductivity, Gel electrophoresis (SDS Page or Western Blot), Potency and ELISA

o Knowledge in Empower and LIMS.

o Knowledge in Microsoft Office.

• Problem solving o Solves problems and implements corrective actions using six sigma tools.

• Be a subject matter expert in given areas of responsibilities and able to solve issues related to his/her area of expertise.

• Knowledge in safety principles, practices, regulations and procedure related to the work

More about us:

At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.

Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

Empowering our people to shine:

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law.

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description

About the role:

This position is required perform all tasks associated with the QC analytical lab operations which include chemical analysis, biochemical analysis, equipment calibration/maintenance, records review, records approval, deviation/investigation write up/review, equipment qualification, method validation, method transfer and other tasks as assigned.

How you will contribute:

Core Responsibilities:

• Perform chemistry, biochemistry analysis of in-process samples, bulk drug substance (BDS), non-routine samples.

• Ensure tests assigned are performed in a timely manner in compliance to Standard Operating procedures

• Perform equipment calibration and maintenance.

• Perform review/approval of QC records/ log books.

• Perform trending of lab results.

• Initiate, participate and complete in Out Of Specification (OOS), Invalid test and Lab Deviation Investigation/ Write-Up and assist in timely closure of laboratory invalid results, lab investigation and CAPA with minimum guidance

• Write/revise SOPs, forms, training qualifications (TQ) and risk assessments (RA).

• Act as a Subject Matter Expert (SME) to provide technical advice to QC Personnel in laboratory related troubleshooting, e.g. lab equipment failure, method

• Provide appropriate training for the QC Analytical Team.

• Participate in method validation/ transfer or equipment qualification when necessary

• Ensure proper, safe handling and disposal of wastes; ensuring a safe working environment

General Responsibilities:

• Carry out 5S and ensures good housekeeping of Analytical Lab area.

• Support and participates in Operation Excellence initiatives (such as GEMBA and GMP walk).

• Lead in cross functional investigation.

• Coach and mentor junior Chemist.

• Participate in projects towards improving safety performance and continuous improvement initiatives

• Demonstrate strong technical knowledge and associated regulatory expectation.

• QC Chemist may cover for another QC Chemist of similar functions/areas in his/her absence by signing documents on his/her behalf.

• Assist Supervisor to support internal and external compliance audits.

• Responsibility to adhere to any applicable EHS requirements.

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

• Any other duties as assigned by supervisor

What you bring to Takeda:

Education and Experience Requirements

• The candidate should have at least a Degree in pharmaceutical sciences, life sciences, biology, biotechnology chemistry, chemical engineering, or a related discipline.

• Certification and trainings such as auditor training or QP training will be advantageous.

• A minimum experience of 10 years, with 5 years of supervisory position, in the pharmaceutical or biotechnology in quality assurance, GMP compliance, operations or validation, ideally in a multinational company.

• FDA/EU cGMP know-how and a thorough understanding of ICH guidelines, together with exposure to the international regulatory network.

• Able to logically solve problems in order to find timely solutions.

• An ability to interact and communicate with all types of personalities in an effective and diplomatic manner

• Good decision-making capability

Key Skills and Competencies

• Project Management Skills

o Organization and planning skills

o Analytical and Logical thinking skills

o Ability to work and collaborate within the team and with cross departments

• Technical Skills

o Has substantial knowledge and understanding in terms of regulatory standards requirements e.g. USP, EP, 21CFR, ICH etc.

o Knowledge in Ion Chromatography (IC), High Performance Liquid Chromatography (HPLC), Fluorescence spectrometer (FLS), pH, Conductivity, Gel electrophoresis (SDS Page or Western Blot), Potency and ELISA

o Knowledge in Empower and LIMS.

o Knowledge in Microsoft Office.

• Problem solving o Solves problems and implements corrective actions using six sigma tools.

• Be a subject matter expert in given areas of responsibilities and able to solve issues related to his/her area of expertise.

• Knowledge in safety principles, practices, regulations and procedure related to the work

More about us:

At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.

Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

Empowering our people to shine:

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law.

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