404 Quality Control Analyst jobs in Singapore

Roles & Responsibilities

About SCG

SCG Cell Therapy Pte Ltd is a Singapore based clinical-stage biotechnology company focusing on the development of novel immunotherapies for patients with pathogenic infections and associated cancers.

WHAT WE'LL OFFER YOU:

• The opportunity is based at the global headquarters of a fast-growing pre-IPO company dedicated to making positive differences in people's health. SCG is a company that provides employees with clear motivational goals and has a strong and positive employer brand in our field.
• A chance to develop your skills and advance in your career in a rapidly evolving business environment. This position is new in our organization, and thus you will have an excellent opportunity to impact the role and its responsibilities, build up a strong team and grow together with the company. This position offers significant career growth opportunity as the business is entering into a fast growth phase and high visibility to senior level management.
• A culture that is transparent, ambitious, international and where a team of experienced professionals with diverse backgrounds share a passion for helping patients and families in need.

Job Description

The candidate will perform routine assays and assist the QC team leader in validating new assays used for in-process and final product release testing. The candidate will also be expected to support the routine maintenance and upkeep of the QC laboratory, and contribute to the continuous improvement of QC processes.

Core responsibilities

• Conduct scheduled in-process and product release testing
• Evaluate test data and generate test reports
• Conduct environmental monitoring of cleanrooms
• Draft standard operating procedures and QC related work instructions
• Support routine QC laboratory operations
• Contribute to the continuous improvement of QC procedures and processes
• Assist in the development, optimization and qualification of new test methods
• Apply good documentation practices on all records

Role requirements

• Diploma or Degree in the chemical or life sciences
• Candidates with cleanroom experience preferred
• Experience with cleanroom environmental monitoring would be advantageous
• Experience with cell and tissue cultures, flow cytometry, qPCR and plate-based fluorescence assays would be advantageous
• Assay development experience is a plus
• Experience with regulatory audits is a plus
• Candidates familiar with GDocP, cGMP, and GLP principles preferred

Tell employers what skills you have

qPCR
Cell
Preventive Maintenance
Assay Development
Raw Materials
Chemistry
Biotechnology
Flow Cytometry
Audits
Team Leader
Life Sciences
Laboratory
Test Data
Cell Therapy
Calibration
GLP

Job Title: Quality Control Specialist

Responsibilities and Tasks:

• Perform routine and non-routine lab testing for raw materials, in-process samples, and finished products.
• Make decisions based on QC test results and troubleshoot issues as needed.
• Provide technical support and guidance to production staff and assume laboratory leadership during off-hours.
• Maintain laboratory equipment, calibration records, and quality documentation.
• Lead short-term QC projects and investigations into customer complaints.
• Communicate results clearly with cross-functional teams to ensure product quality.
• Mentor and support new team members in laboratory procedures and safety protocols.

Requirements and Qualifications:

• Degree in Chemistry or a related field.
• Internship or hands-on experience in a QC or laboratory environment preferred.
• Strong analytical skills and attention to detail.
• Effective communication skills and ability to remain composed under pressure.
• Able to work independently during night/weekend shifts.

Benefits and Compensation Package:

• Shift allowances for 12-hour rotating shifts – Day/Night
• Permanent role with comprehensive benefits package

Roles & Responsibilities

• Conduct quality checks on final product according to established procedures.
• Keep proper record of all analysis results.
• Identify and raise a nonconformance form when the product quality does not meet the specification.
• Provide support to the Production, R&D or Sales departments on an ad-hoc basis.
• Perform calibration and maintenance of lab equipment as planned.
• Properly store and label all retained samples and documentation in the designated storage area.
• Ensure compliance to statutory and corporate requirements related to Health, Safety, Environment and Quality.

By sending your job application/resume to us, it shall be deemed that you have agreed and hereby give your consent to MANFIELD in collecting, using and/ or disclosing your personal data for the purpose of accessing and processing your job application and/ or for future job opportunities within MANFIELD and/ or with the client(s) of MANFIELD. If you wish to withdraw your consent, please notify us. Kindly visit our company website for more information on the Privacy Policy.

WE REGRET TO INFORM THAT ONLY SHORTLISTED CANDIDATES WILL BE NOTIFIED

Manfield Employment Services Pte Ltd (Lic. No: 95C2823)

Posting Personnel: Quennie Chen

EA Personnel Reg No.: R1222837

Tell employers what skills you have

Troubleshooting
Housekeeping
Inventory
Information Management
ISO
Chromatography
Investigation
Purchasing
Raw Materials
ISO 9001
LIMS
Reagent
Laboratory
Manufacturing
Analytical Instruments
Calibration

• Conduct quality checks on final product according to established procedures.
• Keep proper record of all analysis results.
• Identify and raise a nonconformance form when the product quality does not meet the specification.
• Provide support to the Production, R&D or Sales departments on an ad-hoc basis.
• Perform calibration and maintenance of lab equipment as planned.
• Properly store and label all retained samples and documentation in the designated storage area.
• Ensure compliance to statutory and corporate requirements related to Health, Safety, Environment and Quality.

By sending your job application/resume to us, it shall be deemed that you have agreed and hereby give your consent to MANFIELD in collecting, using and/ or disclosing your personal data for the purpose of accessing and processing your job application and/ or for future job opportunities within MANFIELD and/ or with the client(s) of MANFIELD. If you wish to withdraw your consent, please notify us. Kindly visit our company website for more information on the Privacy Policy.

WE REGRET TO INFORM THAT ONLY SHORTLISTED CANDIDATES WILL BE NOTIFIED

Manfield Employment Services Pte Ltd (Lic. No: 95C2823)

Posting Personnel: Quennie Chen

EA Personnel Reg No.: R1222837

About SCG

SCG Cell Therapy Pte Ltd is a Singapore based clinical-stage biotechnology company focusing on the development of novel immunotherapies for patients with pathogenic infections and associated cancers.

WHAT WE'LL OFFER YOU:

• The opportunity is based at the global headquarters of a fast-growing pre-IPO company dedicated to making positive differences in people's health. SCG is a company that provides employees with clear motivational goals and has a strong and positive employer brand in our field.
• A chance to develop your skills and advance in your career in a rapidly evolving business environment. This position is new in our organization, and thus you will have an excellent opportunity to impact the role and its responsibilities, build up a strong team and grow together with the company. This position offers significant career growth opportunity as the business is entering into a fast growth phase and high visibility to senior level management.
• A culture that is transparent, ambitious, international and where a team of experienced professionals with diverse backgrounds share a passion for helping patients and families in need.

Job Description

The candidate will perform routine assays and assist the QC team leader in validating new assays used for in-process and final product release testing. The candidate will also be expected to support the routine maintenance and upkeep of the QC laboratory, and contribute to the continuous improvement of QC processes.

Core responsibilities

• Conduct scheduled in-process and product release testing
• Evaluate test data and generate test reports
• Conduct environmental monitoring of cleanrooms
• Draft standard operating procedures and QC related work instructions
• Support routine QC laboratory operations
• Contribute to the continuous improvement of QC procedures and processes
• Assist in the development, optimization and qualification of new test methods
• Apply good documentation practices on all records

Role requirements

• Diploma or Degree in the chemical or life sciences
• Candidates with cleanroom experience preferred
• Experience with cleanroom environmental monitoring would be advantageous
• Experience with cell and tissue cultures, flow cytometry, qPCR and plate-based fluorescence assays would be advantageous
• Assay development experience is a plus
• Experience with regulatory audits is a plus
• Candidates familiar with GDocP, cGMP, and GLP principles preferred

PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their cost-effective and high-standard healthcare products. At PharmEng Technology, we strive to cultivate the best working environment where empowerment, passion and perseverance are nurtured while serving our clients to achieve their unique business goals. We are seeking an experienced Quality Control Analyst with experience in pharmaceutical company/Life Science industries for a role in Singapore.

Key Responsibilities:

• Sample storage and management
• Prepare and support analytical testing
• Analytical testing and documentation
• Perform lab housekeeping activities
• Perform administrative documentation
• Comply with all HSE guidelines
• Detect and report potential accident, risks and propose solutions
• Responsible for participating in initial training and retraining

Qualifications:

• Proficient in English.
• Previous experience working in a laboratory environment in the pharmaceutical industry (quality assurance, production).
• Nitec or Diploma holders

This position is for 12-hr day shift, 2-3-2 basis.

Why PharmEng Technology?

Our consultants come from different areas of the Pharmaceutical/Biotech/Medical Device industries and have extensive experiences obtained from world-class organizations in North America, Europe, and Asia. At PharmEng Technology, we value everyone’s unique talents and work together to support our clients. We offer continuous career growth, competitive wages, opportunities for travel and a team mentality that sets us apart from our competitors. It is the growth of our staff that continues to grow our company globally.

EEOC Statement

At PharmEng Technology, we don’t just accept difference — we celebrate it, we support it, and we thrive on it for the benefit of our employees, our clients, and our community. PharmEng Technology is proud to be an equal opportunity workplace.

Roles & Responsibilities

Job Summary:

We are seeking a skilled QC Analyst with 3–6 years of experience in pharmaceutical quality control laboratories. This role will support analytical testing, stability programs, and GMP compliance activities to ensure the integrity and timely release of pharmaceutical products and materials. The ideal candidate will have hands-on experience with cGMP practices, analytical instrumentation, and strong documentation skills.

Key Responsibilities:

• Analytical Testing: Perform routine and non-routine testing of raw materials, intermediates, drug substances/products, packaging materials, and complaint samples.

• Stability Programs: Manage sample storage, execute stability testing, and ensure documentation complies with regulatory standards.

• Compliance & Documentation: Ensure activities are aligned with cGMP/cGLP, ALCOA+ principles, and data integrity requirements.

• Equipment Management: Operate, calibrate, maintain, and qualify laboratory instruments and systems.

• HSE & Lab Safety: Follow health, safety, and environmental guidelines; proactively identify and mitigate risks.

• Support Investigations: Participate in deviation investigations, CAPAs, and audit readiness.

• Collaboration: Work cross-functionally with QA, production, and R&D for continuous improvement and issue resolution.

Requirements:

• Diploma or Bachelor's degree in Chemistry, Pharmaceutical Sciences, or related field.

• 3–6 years of hands-on experience in a GMP pharmaceutical QC lab setting.

• Knowledge of analytical techniques such as HPLC, GC, UV, FTIR, etc.

• Experience with LIMS and other quality systems (preferred).

• Strong understanding of regulatory requirements (FDA, EMA, ICH).

• Proven ability to document results accurately and follow SOPs.

• Strong attention to detail and commitment to quality.

• Good communication and teamwork skills.

To Apply, please kindly email your updated resume to

Regret to inform that only shortlisted candidates will be notified.

CEI: R25127749

EA License: 14C7275

Tell employers what skills you have

FTIR
Quality Control
HPLC
GMP
Documentation Skills
Raw Materials
Chemistry
LIMS
Analytical Techniques
Regulatory Requirements
Instrumentation
Teamwork Skills
UV
Laboratory
Audit
Calibration

**Position: Quality Control Senior Analyst (Raw Material)**
+ Hiring Manager: Manager, QC Raw Material & Lab Service
+ Location: Tuas, Singapore
**About the job:**
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
Sanofi has added two new Evolutive Facilities to our global industrial footprint. These production units (EVF) 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 Evolutive Facilities (EVF) will enable more responsive and flexible manufacturing across multiple vaccine and biological platforms including mRNA, while minimize our impact to the environment. Our EVFs will help improve people's lives by giving them faster access to more treatments.
In this context, we are looking for one Quality Control Senior Analyst (Raw Material) to support raw material testing and participate in the setting up of the new QC laboratory for our new site based in Singapore.
**Main responsibilities:**
+ Responsible for QC test for raw material samples including compendial tests and identification tests.
+ Participate in method validation/ verification for raw material testing.
+ Perform QC sampling of incoming raw materials.
+ Author/ revise raw material specification and other QC related documents.
+ Support the laboratory start-up activities, participate in equipment qualification activities including generation of user requirement specifications.
+ Support laboratory activities such as housekeeping and equipment maintenance.
+ Train newcomers for QC lab activities and testing
+ Participate and contribute to laboratory continuous improvement.
+ Contribute to laboratory performance (eg, deviation/OOS rate, sample turnaround time)
**Education and Experience**
+ Bachelor's or Master's Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology or related life Sciences or Technology with at least 4-5 years of experience in QC lab operations and raw material testing.
+ Experience in method validation/ verification in the pharmaceutical or biotechnology industry preferred.
**Key technical competencies and soft skills:**
+ Good understanding of good laboratory practices, good documentation practice and data integrity requirements.
+ Discipline and assertiveness in decision-making and execution in laboratory start-up activities. Experienced in routine laboratory operations and continuous improvements.
+ Experienced/participated in method transfer, method validation and method verification for raw material testing will be advantageous.
+ Experienced in start-ups will be advantageous.
+ Fluent in English speaking and writing.
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (

Roles & Responsibilities

Salary: Up to $4500

Duration: 1 Year

Working Days & Hours: 5 days Office Hours

Location: TUAS

Key Responsibilities:

• Job Responsibilities
• To prioritize and perform the various testing/analysis (EM and bioassays i.e. air sampling, surface viable sampling, total particulate sampling etc.) in timely manner.
• Analysis of bulk product according to Standard Operating Procedures and Test Methods.
• Documentation of results in accordance with current Good Manufacturing Practices (cGMP).
• Problem solving of analytical methods as well as troubleshooting of equipment.
• Involvement in method transfers and validation.
• Involved in equipment qualification and technical selection of QC equipment and/or standards and reagents.
• Generation of required trending and reporting information, document revision and update.
• Support / Perform OOS, deviation investigations. Draft investigations reports.
• General lab support including housekeeping, equipment maintenance, inventory of supplies, lab supplies ordering, management of glass wares, autoclaving etc.
• Any other duties as assigned by your Supervisor/Manager

Job Requirements:

• Minimum Degree in Biochemistry, Microbiology or other related fields
• Relevant experience would be good

Interested candidates, please submit your resume to:

Ally Audrey Lok Xin Woon

Recruit Express Pte Ltd (Healthcare & Lifescience)

Company EA Licence number : 99C4599

Personnel EA License: R21102307

Tell employers what skills you have

Biochemistry
Sampling
Troubleshooting
Housekeeping
Inventory
Healthcare
Microbiology
Problem Solving
Equipment Maintenance
Equipment Qualification
Air Sampling
Manufacturing