496 Quality Control Analyst jobs in Singapore

About the Role:

We are looking for a QC Analyst (Microbiology) to support our QC lab operations, ensuring testing and documentation are completed accurately and in compliance with cGMP standards.

Responsibilities:

• Perform routine microbiological testing of raw materials, drug substances, finished products, and packaging/stability samples.
• Manage sample handling, storage, and documentation.
• Ensure compliance with cGxP, GMP, HSE, and data integrity requirements.
• Support audits, inspections, and laboratory equipment documentation.

Requirements:

• Diploma/Degree in Microbiology, Biotechnology, Life Sciences, or related field.
• Preferably with lab or pharmaceutical industry experience.
• Knowledge of aseptic techniques, microbiological methods, and GxP standards an advantage.
• Strong attention to detail, teamwork, and communication skills.

Why Join Us?

• Be part of a global biotech/pharma company committed to quality and patient safety.
• Gain hands-on laboratory experience in a regulated environment.
• Continuous learning and professional growth opportunities.
• Collaborative and supportive work culture.

Responsibilities:

• Conduct conformance test on raw materials and finished products.
• Create and maintain inspection reports and records
• Ensure raw materials and finished product meat quality specifications before material release
• Reporting quality issues to relevant stakeholders
• Working with other departments (e.g., procurement, production) to address quality issues.
• Communicating with suppliers regarding quality concerns.
• Collaborating with management on quality-related initiatives.
• Support elements of site's quality system, including internal audit, pest control, and sanitation

Requirements:

• Diploma in food science or related field
• Able to commit in minimum 6-month contract role
• Able to start work in short notice
• Work location: Boon Lay
• Working hours: 8am-5pm

Ong Yvonne 

Personnel Reg No: R

Manpower Staffing Services (S) Pte Ltd

EA Licence No: 02C3423

About the Role

We are seeking a QC Analyst to support quality control operations within our biotech drug substance site. The role is responsible for executing laboratory testing, sample management, and equipment maintenance in compliance with cGxP standards, ensuring the quality and timely delivery of products.

Key Responsibilities

• Perform analytical testing and documentation of raw materials, drug substances, drug products, packaging, complaints, and stability samples
• Manage sample storage and stability programs
• Maintain, calibrate, and qualify laboratory equipment
• Ensure compliance with cGxP, data integrity, and HSE guidelines
• Participate in training and contribute to continuous improvement initiatives

Performance Measures

• Accurate and timely completion of analysis and documentation
• Compliance with GMP, SOPs, and regulatory standards
• Readiness for inspections with no critical findings
• Contribution to cost and process optimization

Qualifications & Experience

• Diploma, apprenticeship, or equivalent training in a relevant scientific field (e.g., Chemistry, Biochemistry, Biotechnology, Life Sciences)
• Preferably with 2-5 years of experience in a pharmaceutical laboratory environment (QC, QA, or production)
• Knowledge of GMP/cGxP standards, laboratory techniques, and QC processes
• Strong teamwork, resilience, and problem-solving skills
• Basic proficiency in English

Why Join Us

This role offers the opportunity to directly impact product quality, compliance, and patient safety while working in a collaborative and innovative environment.

About the Role:

We are looking for a QC Analyst (Microbiology) to support our QC lab operations, ensuring testing and documentation are completed accurately and in compliance with cGMP standards.

Responsibilities:

• Perform routine microbiological testing of raw materials, drug substances, finished products, and packaging/stability samples.
• Manage sample handling, storage, and documentation.
• Ensure compliance with cGxP, GMP, HSE, and data integrity requirements.
• Support audits, inspections, and laboratory equipment documentation.

Requirements:

• Diploma/Degree in Microbiology, Biotechnology, Life Sciences, or related field.
• Preferably with lab or pharmaceutical industry experience.
• Knowledge of aseptic techniques, microbiological methods, and GxP standards an advantage.
• Strong attention to detail, teamwork, and communication skills.

Why Join Us?

• Be part of a global biotech/pharma company committed to quality and patient safety.
• Gain hands-on laboratory experience in a regulated environment.
• Continuous learning and professional growth opportunities.
• Collaborative and supportive work culture.

Key Responsibilities
Manage the storage and inventory of laboratory samples
Conduct analytical testing and documentation for APIs, drug substances/products, complaints, packaging materials, and stability samples
Ensure strict compliance with cGxP standards, including data integrity requirements
Execute and document stability testing (if not centralized), including storage, testing, and reporting to cGxP standards
Follow all Health, Safety, and Environment (HSE) guidelines
Identify and report safety risks or potential incidents, and propose preventive solutions
Participate in mandatory training and retraining programs
Support operations during rotating day/night shifts
Role Requirements
Essential Qualifications and Experience
Prior experience in a laboratory setting within the pharmaceutical industry (QA, production), with exposure to aseptic techniques preferred
Proficiency in administrative and documentation tasks compliant with GMP and HSE standards
Demonstrated strengths in:
Breakthrough analysis and problem-solving
Resilience and adaptability
Operational efficiency and continuous learning
Digital fluency and technical skills
Technical Competencies
Hands-on knowledge of laboratory instruments and QC testing procedures
Strong command of GxP, TQM principles, and lab excellence standards
Ability to maintain QC IPC/DS laboratory equipment and systems in accordance with cGMP compliance
Competent in executing product testing within timelines and contributing to validation and method transfer protocols
Skilled in performing routine in-process, release, and stability testing, including documentation review
Capable of supporting lab investigations and leading root cause analysis
Detail-oriented in preparing and verifying QC documentation to ensure accuracy, consistency, and regulatory compliance
Proactively identifies opportunities to optimize testing procedures
Supports audit readiness and participates in internal audits and inspections by health authorities
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Overview
Join our best-in-class QA team at our state-of-the-art Singapore site, where you’ll gain exposure to advanced biopharmaceutical processes, drive quality initiatives, and build your expertise in a collaborative and high-performance environment.
This is a 12-month contractual position under Quality Control team.
Responsibilities
Understanding and execution of biochemical analyses such as cell counts, flow cytometry, ELISA, PCR analysis, and compendial testing (pH, Conductivity, Appearance) as per USP, JP, and EP standards.
Documentation and review of results in accordance with current Good Manufacturing Practices (cGMP).
General lab support including housekeeping, equipment maintenance, inventory of supplies, lab supplies ordering, management of glassware, autoclaving, etc.
Support sample logistics area including retention sample storage, external lab testing, QC documents control, and shipment of QC samples. Prepare and maintain standards and reagents as required by GMP documents. Responsible to follow data integrity requirements.
Actively contribute to operational efficiency and continuous improvement initiatives. Problem solving of analytical methods as well as troubleshooting of equipment.
Involvement in equipment qualification, maintenance and troubleshooting. Support / perform OOS, deviation investigations. Draft investigation reports.
Any other duties as assigned by your Supervisor/Manager.
Qualifications
Degree/Diploma in a relevant science field or equivalent
0-5 years’ experience in Quality Control
Strong knowledge of microbiological laboratory operations in a manufacturing environment
Demonstrates an ability and desire to learn from experience
Good problem solving and analytical skills
Good communication skills
Note: Applications will be considered upon receipt of the application through the provided link.
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Why working at Eurofragance?

In Eurofragance you will be part of the exciting world of smells and fragrances.

You will grow and learn in a company in constant growth and expansion.

You will have the opportunity to develop your career working with top professionals.

You will be part of a Global Company with Headquarters in Spain and subsidiaries in Dubai, Singapore, Mexico, Turkey, and India among others.

You will practice your language skills in a global and multicultural environment.

You will feel you play a role in society thanks to our Corporate Social Responsibility policy and our commitment to the Environment, which we demonstrate on a day-to-day basis with actions such as the Volunteer Day.

We are Passion, Performance & Entrepreneurship, we are Eurofragance

Enjoy a great work environment in Eurofragance

At our company, we're committed to creating an inclusive work environment where everyone feels welcome, regardless of their gender, age, sexual orientation, or any other factor. We encourage candidates from all walks of life to apply for this job vacancy, and we extend a particularly warm welcome to those with disabilities.

JOB MISSION:

The principal objective of this position is to carry out routine tasks related to quality control (QC) of raw materials and finished products to uphold quality standard of the company.

This person will need to prioritize urgencies accordingly and coordinate with relevant departments and/or parties.

MAIN JOB FUNCTIONS:

• Perform routine QC testing, which includes organoleptic, physical-chemical and chromatographic analyses.
• Interpret and evaluate analysis results against established standards and specifications for product releases and/or rejections.
• Assist in the investigations for quality non-conformances.
• Responsible for clear entry of quality data and information.
• Maintain good housekeeping in the laboratory and sample retention room.
• Ensure the smooth operations of the laboratory with periodic checks and in-house maintenance of laboratory instruments/equipment.

EDUCATION & EXPERIENCE REQUIRED:

• Minimally a diploma in science related field(s), preferably chemistry or perfumery.
• Minimum of 1 year of relevant work experience in a laboratory, preferably in a quality control department.
• Knowledge with SAP and/or hands-on experience with gas chromatography is preferred.
• Fresh graduates are welcome to apply.
• Related experiences in a fragrance or flavour industry will also be considered. A basic olfactory test will be carried out

In Eurofragance you will be part of the exciting world of smells and fragrances.
You will grow and learn in a company in constant growth and expansion.
You will have the opportunity to develop your career working with top professionals.
You will be part of a Global Company with Headquarters in Spain and subsidiaries in Dubai, Singapore, Mexico, Turkey, and India among others.
You will practice your language skills in a global and multicultural environment.
You will feel you play a role in society thanks to our Corporate Social Responsibility policy and our commitment to the Environment, which we demonstrate on a day-to-day basis with actions such as the Volunteer Day.
We are Passion, Performance & Entrepreneurship, we are Eurofragance!
Enjoy a great work environment in Eurofragance!
At our company, we're committed to creating an inclusive work environment where everyone feels welcome, regardless of their gender, age, sexual orientation, or any other factor. We encourage candidates from all walks of life to apply for this job vacancy, and we extend a particularly warm welcome to those with disabilities.
JOB MISSION:
The principal objective of this position is to carry out routine tasks related to quality control (QC) of raw materials and finished products to uphold quality standard of the company.
This person will need to prioritize urgencies accordingly and coordinate with relevant departments and/or parties.
MAIN JOB FUNCTIONS:
Perform routine QC testing, which includes organoleptic, physical-chemical and chromatographic analyses.
Interpret and evaluate analysis results against established standards and specifications for product releases and/or rejections.
Assist in the investigations for quality non-conformances.
Responsible for clear entry of quality data and information.
Maintain good housekeeping in the laboratory and sample retention room.
Ensure the smooth operations of the laboratory with periodic checks and in-house maintenance of laboratory instruments/equipment.
Requirements
EDUCATION & EXPERIENCE REQUIRED:
Minimally a diploma in science related field(s), preferably chemistry or perfumery.
Minimum of 1 year of relevant work experience in a laboratory, preferably in a quality control department.
Knowledge with SAP and/or hands-on experience with gas chromatography is preferred.
Fresh graduates are welcome to apply.
Related experiences in a fragrance or flavour industry will also be considered. A basic olfactory test will be carried out
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Quality Control Analyst (QC/Food Science/Contract)
Join to apply for the
Quality Control Analyst (QC/Food Science/Contract)
role at
Manpower Singapore
Quality Control Analyst (QC/Food Science/Contract)
Join to apply for the
Quality Control Analyst (QC/Food Science/Contract)
role at
Manpower Singapore
Conduct conformance test on raw materials and finished products.
Create and maintain inspection reports and records
Ensure raw materials and finished product meat quality specifications before material release
Reporting quality issues to relevant stakeholders
Working with other departments (e.g., procurement, production) to address quality issues.
Communicating with suppliers regarding quality concerns.
Collaborating with management on quality-related initiatives.
Support elements of site’s quality system, including internal audit, pest control, and sanitation
Responsibilities
Conduct conformance test on raw materials and finished products.
Create and maintain inspection reports and records
Ensure raw materials and finished product meat quality specifications before material release
Reporting quality issues to relevant stakeholders
Working with other departments (e.g., procurement, production) to address quality issues.
Communicating with suppliers regarding quality concerns.
Collaborating with management on quality-related initiatives.
Support elements of site’s quality system, including internal audit, pest control, and sanitation
Requirements
Diploma in food science or related field
Able to commit in minimum 6-month contract role
Able to start work in short notice
Work location: Boon Lay
Working hours: 8am-5pm
Seniority level
Seniority level Entry level
Employment type
Employment type Contract
Job function
Job function Quality Assurance
Industries Staffing and Recruiting
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