1,374 Qc Analyst jobs in Singapore

Job Description & Requirements

• Conducts daily laboratory analysis of raw materials, quality control stability sample testing, in-process testing, finished products and other related testing.
• Prepare test solutions, volumetric solutions, standardization of volumetric solutions and reference standards.
• Able to plan, schedule and assisting in supervising QC testing for finished product, raw materials & stability products.
• Assist to ensure QC testing of products are completed on time, review / approve test report and able to forward the test reports /or samples to QA when required.
• Able to conduct laboratory investigation when required.
• Ensures and maintains cleanliness and safety of the QC laboratory according to the Good Laboratory Practices.
• Performs routine calibration & preventive maintenance for analytical instrument and report any deviation.
• Assists the QC team in new assigned projects.
• Performs products validation, cleaning validation and method validation.
• Conducts microbiological testing and environment monitoring as backup if assigned.
• Any other ad hoc tasks assigned.

Requirements:

• Minimum Diploma holder in Chemistry / Chemical Engineering / Bioscience / Life Science / Pharmaceutical / QA & QC.
• Some prior experience preferred in QA & QC.

Other information :

• 5 days work week .
• Permanent position with 2 years lock-in period.

Adecco is partnering with a reputable pharma MNC.

• Focus: Perform analytical testing, stability studies, and laboratory equipment maintenance in a GMP QC environment
• Office location: Singapore
• Working hours: 12h rotating shifts (work 3 days, off 2 days)

• Min Diploma or equivalent in Chemistry, Pharmaceutical Sciences, or related discipline
• 1-3 years of hands-on experience in a pharmaceutical QC laboratory
• Proficient in analytical testing of APIs, drug substances, and stability samples
• Experience in GMP environments with strong knowledge of GxP and data integrity requirements
• Familiar with lab instrumentation, equipment qualification, and calibration processes
• Detail-oriented, with strong documentation and organizational skills
• Ability to identify and suggest process improvements to enhance testing efficiency
• Strong teamwork and communication skills, with readiness to support audits and inspections

As QC Analyst (chemistry), you will be responsible for executing analytical testing and supporting lab operations to ensure timely product release and compliance with regulatory standards.

• Conduct routine analytical testing and documentation for raw materials, drug substances, and packaging materials
• Perform testing and sample management for stability studies in accordance with cGMP standards
• Maintain and calibrate laboratory equipment and support qualification activities
• Ensure accurate documentation and data entry in compliance with data integrity requirements
• Collaborate with QA and cross-functional teams to support timely batch release
• Participate in internal audits and health authority inspections when required
• Contribute to identifying and implementing lab process improvements
• Comply with all health, safety, and environmental (HSE) regulations

• Send your resume to:
• Email Topic: Job Application - QC Analyst (Chemistry)
• We regret to inform that only shortlisted candidates will be contacted.

Lim Jia Yi

EA License Number: 91C2918

Personnel Registration Number: R

Lim Jia Yi

EA License No: 91C2918

Personnel Registration Number: R

• Adecco is partnering with a reputable pharma MNC.

# The Opportunity

• Focus: Support microbiological testing and sample management in a GMP-regulated QC laboratory
• Office location: Tuas
• Working hours: 12h rotating shifts (work 3 days, off 2 days)

# The Talent

• Min Diploma or equivalent in Microbiology, Biotechnology, or relevant scientific discipline
• 1-2 years of hands-on experience in a microbiology or pharmaceutical QC lab
• Familiar with microbiological testing techniques and aseptic handling
• Knowledge of GxP regulations, data integrity, and lab safety standards
• Previous experience as a QC Microbiology Analyst or Lab Technician preferred
• Strong attention to detail, documentation accuracy, and willingness to learn
• Clear and concise communication skills; able to follow written procedures effectively

# Main Functions

As QC Analyst - Microbiology, you will support daily operations in the QC microbiology lab, ensuring timely testing, data accuracy, and regulatory compliance.

• Conduct microbiological testing on drug substances, raw materials, and stability samples
• Manage sample storage, labeling, and dispatch in accordance with GMP standards
• Support lab operations including documentation, SAP data entry, and equipment upkeep
• Ensure timely execution of testing and sample handling with minimal deviation
• Participate in lab inspections, audits, and contribute to a state of inspection readiness
• Complete all required training and contribute to continuous improvement initiatives
• Comply with HSE and quality guidelines in all laboratory activities

# Next Step

• Send your resume to:
• Email Topic: Job Application - QC Analyst Microbiology
• We regret to inform that only shortlisted candidates will be contacted.

Lim Jia Yi

EA License Number: 91C2918

Personnel Registration Number: R

Lim Jia Yi

EA License No: 91C2918

Personnel Registration Number: R

Responsibilities:

• Ensure compliance to statutory and corporate requirements related to Health, Safety, Environment and Quality.
• 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.

Requirements:

• GCE 'O' Level / Nitec / Higher Nitec / Diploma
• Entry Level - No prior experience required - OJT will be provided
• Willing to work in Jurong Island

___

HOW TO APPLY :

Interested candidates, please submit your resume by clicking on "Quick Apply"

Please provide following information in the resume for immediate processing

1) Reasons for leaving current and/or last employment

2) Last drawn and/or current salary

3) Expected salary

4) Date of availability and/or Notice Period

All applications will be treated in strictest confidence and only shortlisted candidates will be notified

Joni

EA License No : 03C5391

EA Reg No : R

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 analyses 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 and local language

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.

Responsibilities:

• Conduct conformance test on raw materials and finished products.
• Create and maintain inspection reports and records
• Ensure raw materials and finished product meet 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:

• ITE/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

Job Description & Requirements

• Conducts daily laboratory analysis of raw materials, quality control stability sample testing, in-process testing, finished products and other related testing.
• Prepare test solutions, volumetric solutions, standardization of volumetric solutions and reference standards.
• Able to plan, schedule and assisting in supervising QC testing for finished product, raw materials & stability products.
• Assist to ensure QC testing of products are completed on time, review / approve test report and able to forward the test reports /or samples to QA when required.
• Able to conduct laboratory investigation when required.
• Ensures and maintains cleanliness and safety of the QC laboratory according to the Good Laboratory Practices.
• Performs routine calibration & preventive maintenance for analytical instrument and report any deviation.
• Assists the QC team in new assigned projects.
• Performs products validation, cleaning validation and method validation.
• Conducts microbiological testing and environment monitoring as backup if assigned.
• Any other ad hoc tasks assigned.

Requirements:

• Minimum Diploma holder in Chemistry / Chemical Engineering / Bioscience / Life Science / Pharmaceutical / QA & QC.
• Some prior experience preferred in QA & QC.
• Preferred to have experience in HPLC, UV, IR, Dissolution tester.

Other information :

• 5 days work week .
• Permanent position with 2 years lock-in period.

• Perform testing of incoming raw material samples (e.g., FTIR, identity by wet chemistry, reagent preparation, sample receiving).
• Manage and store raw material samples in compliance with cGMP.
• Perform analytical testing and documentation for raw materials, API, drug substances/products, packaging materials, complaints, and stability samples.
• Conduct stability testing, sample storage, and documentation (if not centralized).
• Maintain QC Raw Materials laboratory in full cGMP compliance.
• Execute method validation/verification and routine release testing for raw materials.
• Perform data entry and review of RM packages for batch release.
• Support laboratory improvement projects, investigations (OOS, deviations), and change controls.
• Prepare for and participate in internal audits and health authority inspections.
• Undertake other duties or projects as assigned by the Section Manager.

• Comply with all HSE policies and guidelines.
• Identify, report, and propose solutions for potential hazards and risks.
• Actively participate in initial and ongoing safety training.

We are assisting our client, a globally renowned leader in specialty chemicals , to hire a dedicated QC Analyst . This is an exciting opportunity to advance your laboratory career with a company that values sustainability, innovation, and employee development.

Join a high-performing, supportive team within a well-established organization with strong operations in Singapore, and play a key role in ensuring product quality and operational excellence.

What's In It for You?

• Salary : Up to $3,500 basic + $900 fixed allowance (for experienced candidates)
• Benefits : Permanent role with AWS + Variable Bonus
• Location : Jurong Island (transport provided from designated points)
• Shifts : 12-hour rotating shifts (Morning/Night) or permanent 12-hour day shift options

Why Join?

• Global Brand, Local Impact – Be part of a respected multinational with a strong footprint in Singapore.
• Career Growth – Access structured training, skill development, and long-term career opportunities.
• Team Culture – Work in a collaborative, safety-first environment.

Key Responsibilities

• Perform routine & non-routine quality testing on raw materials, in-process, and finished products.
• Record and report test results in compliance with QA standards.
• Investigate quality issues and support resolution of supplier/customer concerns.
• Manage calibration and maintenance of laboratory equipment.
• Support training of new lab technicians.
• Ensure full compliance with SHE (Safety, Health & Environment) and QA protocols.

Key Requirements

• Diploma / Degree in Chemistry or related discipline.
• Minimum 2 years' QC or laboratory experience in the chemical industry.
• Willingness to work 12-hour shifts .
  Strong attention to detail, safety mindset, and teamwork spirit.

Ready to make a meaningful impact in a cutting-edge chemical lab? Submit your CV in MS Word format to -

EA Reg No.: R

Triton AI Pte Ltd | EA License No.: 21C0661