102 Lab Qc Analyst Microbiological Up To 4500 6 12 Mth East Sg jobs in Singapore

Up to $4500/mth

6 / 12 mth (can renew/convert)

Good Culture + Benefits!

Job Details

• Working hours: Office Hours

• Location: East

Job Descriptions

• Responsible for ensuring the laboratory operations in accordance to ISO 17025 and cGMP requirements
• Leads, designs and performs method development (i.e. bioassay and mycoplasma) and validation of new test procedures for incoming projects
• Functions as Technical Reviewer for A2LA accredited tests and non-accredited tests
• Evaluates analytical results to form interpretations of data and renders scientific opinions for client-driven projects
• Serves as subject matter expert (SME) in area of specialization, established standards for regulatory compliance
• Serves as technical liaison with Customers with regards to technical services and performs Customer site visits where required
• Participates in internal Quality Audits, System Audits, Audits conducted by external agencies and Regulatory Authorities
• Maintains confidentiality of all Client information according to internal SOPs, Quality Service Agreements, and regulatory requirements

Requirements

• Bachelor of Science or any related field; MSc. preferred but not essential
• Minimum 2-6 years of relevant QC microbiological experience working in an ISO17025 / GMP laboratory environment
• Experience in method validation and development, method transfer, qualification activities in regulated laboratory
• Good knowledge of ISO 17025, cGMP and other regulatory guidelines
• Good understanding/working knowledge of Project Management and Measurement Uncertainty (MU)

*Interested applicants, please apply with your resume with reason(s) for leaving previous employment(s), notice period, last drawn and expected salary.

All applications will be treated with strictest confidentiality. We regret that only shortlisted candidates will be notified.

RecruitFirst Pte Ltd E.A. 13C6342

Joseph Yap Shi Hao (R1767577)

Are you ready to take your lab career to the next level with a globally renowned company that values sustainability, innovation, and employee development? This is your opportunity to join a high-performing, supportive team within a well-established chemicals company with a strong presence in Singapore. They are looking for a QC Analyst who’s passionate about quality and eager to play a key role in supporting manufacturing operations through precise and timely laboratory analysis.

Why Join This Company?

• Global Brand, Local Impact – Be part of a respected multinational company with strong operations in Singapore.
• Career Growth – Enjoy structured training, skill development, and long-term career stability.
• Team Culture – Thrive in a collaborative, safety-first work environment.

What’s In It for You?

• Salary : Up to $3,500 basic + $900 fixed allowance (for experienced candidates)
• Location : Jurong Island – Transport provided from designated pick-up points
• Type : Full-Time Permanent Role with AWS + Variable Bonus
• Shift : 12-hour rotating shifts

Responsibilities:

• Perform routine and 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
• Handle calibration and maintenance of lab equipment
• Support training for new lab technicians
• Maintain strict adherence to SHE (Safety, Health & Environment) and QA protocols

Key Requirements:

• Diploma in Chemistry or related discipline
• Minimum 2 years of QC or laboratory experience in the chemical industry
• Comfortable with 12-hour rotating shift work
• Detail-oriented, safety-conscious, and a strong team player

Ready to make a meaningful impact in a cutting-edge chemical lab?

Submit your resume (in MS Word format) to

EA Reg No.: R1983718
Triton AI Pte Ltd | EA License No.: 21C0661

• Basic Salary: Up to $3,000 + Fixed Allowance: $1,000
• Shift Allowances (12-hour rotating shifts - Day/Night)
• Company Transport Provided from Jurong East to Jurong Island
• Permanent Role with AWS (13th-month bonus) + Variable Bonus

• Conduct 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 where needed
• Provide technical support and guidance to plant operators and assume QC lab leadership during off-hours
• Maintain lab 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 lab procedures and safety

• Degree in Chemistry or related field
• Internship or hands-on experience in a QC or lab environment preferred
• Strong problem-solving skills and attention to detail
• Effective communicator with the ability to stay composed under pressure
• Able to work independently during night/weekend shifts

• Basic Salary: Up to $3,000 + Fixed Allowance: $1,000
• Shift Allowances (12-hour rotating shifts – Day/Night)
• Company Transport Provided from Jurong East to Jurong Island
• Permanent Role with AWS (13th-month bonus) + Variable Bonus

Key Responsibilities:

• Conduct 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 where needed
• Provide technical support and guidance to plant operators and assume QC lab leadership during off-hours
• Maintain lab 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 lab procedures and safety

Key Requirements:

• Degree in Chemistry or related field
• Internship or hands-on experience in a QC or lab environment preferred
• Strong problem-solving skills and attention to detail
• Effective communicator with the ability to stay composed under pressure
• Able to work independently during night/weekend shifts

How to Apply:

Submit your updated CV (in MS Word format) to

Triton AI Pte Ltd
EA License: 21C0661 | Registration No: R1875181

• JUrong Island
• 8.30am to 8.30pm (12 hours rotating shift- Day & Night shift
• Working hours: 8:30am-8:30pm or 8:30pm-8:30am (shift pattern is 222, Eg, Mon and Tues work from 8:30am to 8:30pm. Wed and Thurs (off), Fri and Sat work from 8:30pm to 8:30am continuously.

Allowances: Meal allowance $150/month, shift allowance $550/month.

• Perform accurate and timely laboratory tests and analyses.
• Support daily lab operations and coordinate section activities in the absence of the team leader.

Specific Responsibilities:

• Conduct tests and analyses in accordance with established standards, policies, and procedures, ensuring accurate record-keeping.
• Carry out field assignments or perform testing at site laboratories as required.
• Prepare and standardize reagents and test solutions.
• Review and re-test any suspicious or abnormal results.
• Act as a laboratory representative during third-party and refinery testing.
• Maintain a clean and safe working environment, ensuring proper care of equipment, apparatus, and materials.
• Support the practical training of new analysts when assigned.
• Perform shift work and overtime as necessary.
• Carry out any additional tasks assigned by the supervisor.
• Adhere to high standards of ethics and integrity in accordance with industry best practices.

Requirements:

• Min Diploma in Science, Chemistry, Chemical Engineering, or a related discipline.

Interested applicants may email resume to

Chooi Kelly (CEI Registration No: R25136207)

Recruit Express Pte Ltd (EA: 99C4599)

We regret only shortlisted candidates will be contacted

QC Analyst (Lab/ Shift/ Jurong/ 1 Yr Contract)

More information:

• Salary Up to $4,000 depending on experience
• Location : Gul Circle
• Shift Work with shift and transprot allowance
• Immediate Vacancy

Our client, a well known MNC company in BioPharmaceutical Industry, located in the West is looking for QC Analyst.

Job Purpose

• Reporting to QC Chemist, the incumbent will carry out QC analyses in compliance with Laboratory and Analytical Methods ensuring quality, cGMP, heath, safety and environmental standard are met. Assist in other functions such as documentation and preparation of standard operating procedures.

Responsibilities

• Assist in carrying out on the job training of other QC Analysts, incorporating cGMP and safety procedures.
• Perform and carry out analytical testing in compliance with specifications, Analytical Methods, Laboratory Methods and pharmacopoeia requirements.
• Assist in monitor the calibration and maintenance program for laboratory instruments / equipment and ensure compliance with established schedules.
• Assist in qualification of laboratory equipment and validation of analytical methods.
• Ensure that analyses are carried out and reported in accordance with GLP (Good Laboratory Practices). Ensure that analyses are completed on time and are consistent with business requirements.
• Assist in conducting OOS and atypical results investigation.
• To ensure that qualification, preventive maintenance and calibration of laboratory equipment are carried out.
• Report and trend test results.
• Planning and assurance of cGMP compliant quality testing and documentation according to schedule.
• Prepare laboratory reagents in compliance with GLP and laboratory SOP requirements. Source reagents / laboratory consumables keeping in view department budget targets.
• Assist in other functions such as preparation of standard operating procedures and Assist documentation etc and participate in departmental activities as and when required. Maintenance and development of all required laboratory documents (i.e. raw data sheets, log books).
• Responsible for electronic raw data handling in compliance with regulations and guidelines.
• Responsible for inspection and audit preparedness with respect to cGMP and EHS issues.
• Ensure safe working in the laboratory by practicing and communicating safety.
• Other responsibilities that are not included in the above but are related to quality control and in accordance to internal guidelines and SOP

Requirements:

• Preferably possess a years’ hands-on anlaytical testing experience in a lab environment, from the pharmaceutical industry.
• Familiar with analytical equipments (eg. HPLC, GC etc)
• Must be willing to work shift on rotational basis.
• Must be analytical, methodical and quality conscious.
• Good knowledge of FDA regulations and cGMP.
• Preferably possess a Diploma in chemistry/ chemical process technology / bio-process technology; or a ITE graduate.

Lim Pey Chyi - Apple.lim @ manpower.com.sg .

Recruitment Consultant (R2090579)

Manpower Staffing Services (S) Pte Ltd
EA Licence: 02C3423

QC Analyst (Lab/ Shift/ Jurong/ 1 Yr Contract)

More information:

• Salary Up to $3500 depending on experience
• Location : Gul Circle
• Shift Work with shift and transprot allowance
• Immediate Vacancy

Our client, a well known MNC company in BioPharmaceutical Industry, located in the West is looking for QC Analyst.

Job Purpose

• Reporting to QC Chemist, the incumbent will carry out QC analyses in compliance with Laboratory and Analytical Methods ensuring quality, cGMP, heath, safety and environmental standard are met. Assist in other functions such as documentation and preparation of standard operating procedures.

Responsibilities

• Assist in carrying out on the job training of other QC Analysts, incorporating cGMP and safety procedures.
• Perform and carry out analytical testing in compliance with specifications, Analytical Methods, Laboratory Methods and pharmacopoeia requirements.
• Assist in monitor the calibration and maintenance program for laboratory instruments / equipment and ensure compliance with established schedules.
• Assist in qualification of laboratory equipment and validation of analytical methods.
• Ensure that analyses are carried out and reported in accordance with GLP (Good Laboratory Practices). Ensure that analyses are completed on time and are consistent with business requirements.
• Assist in conducting OOS and atypical results investigation.
• To ensure that qualification, preventive maintenance and calibration of laboratory equipment are carried out.
• Report and trend test results.
• Planning and assurance of cGMP compliant quality testing and documentation according to schedule.
• Prepare laboratory reagents in compliance with GLP and laboratory SOP requirements. Source reagents / laboratory consumables keeping in view department budget targets.
• Assist in other functions such as preparation of standard operating procedures and Assist documentation etc and participate in departmental activities as and when required. Maintenance and development of all required laboratory documents (i.e. raw data sheets, log books).
• Responsible for electronic raw data handling in compliance with regulations and guidelines.
• Responsible for inspection and audit preparedness with respect to cGMP and EHS issues.
• Ensure safe working in the laboratory by practicing and communicating safety.
• Other responsibilities that are not included in the above but are related to quality control and in accordance to internal guidelines and SOP

Requirements:

• Preferably possess a years’ hands-on anlaytical testing experience in a lab environment, from the pharmaceutical industry.
• Familiar with analytical equipments (eg. HPLC, GC etc)
• Must be willing to work shift on rotational basis.
• Must be analytical, methodical and quality conscious.
• Good knowledge of FDA regulations and cGMP.
• Preferably possess a Diploma in chemistry/ chemical process technology / bio-process technology; or a ITE graduate.

Lim Pey Chyi - Apple.lim @ manpower.com.sg .

Recruitment Consultant (R2090579)

Manpower Staffing Services (S) Pte Ltd
EA Licence: 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.

The Company

Our client, a well-established insurance company, is seeking an experienced Financial Reporting Manager for a 12-month contract. The role will be responsible for managing end-to-end financial and regulatory reporting, strengthening internal controls, and supporting ongoing finance transformation efforts in a fast-paced environment.

The Role

· Lead end-to-end financial reporting processes, ensuring compliance with local regulatory and group requirements.

· Oversee technical accounting operations, including control design and documentation.

· Prepare and review financial statements and support submissions to regulatory bodies such as MAS and CPF.

· Partner with audit and compliance teams to manage audit readiness and remediation plans.

· Support ongoing transformation efforts, bringing in best practices and streamlined workflows.

· Guide and mentor junior team members while promoting accountability and excellence.

Your Profile

· Degree in Accounting, Finance, or a related field; professional certifications such as CPA, ACCA, or CA are highly preferred.

· Strong understanding of SFRS and relevant regulatory frameworks.

· Proven experience in financial reporting, including preparation and review of financial statements.

· Prior exposure to regulatory reporting (ie MAS, CPF submissions) within the insurance or financial services sector.

· Solid background in technical accounting and familiarity with internal control frameworks.

· Demonstrated leadership capabilities, ideally in a managerial or supervisory role.

· Strong analytical and financial planning skills with attention to detail.

· Excellent communication and interpersonal skills, with the ability to engage stakeholders across departments.

Ability to work independently and perform under pressure in a fast-paced, deadline-driven environment.

Apply Today

Please send your resume, in WORD format only and quote reference number GO13260062 , by clicking the apply button. Please note that only short-listed candidates will be contacted.

Robert Half International Pte Ltd. Co. Registration no.: 200612189E | EA Licence No.: 07C5595 | Gabriela De Brito Lopes Prestes Oxby EA Registration no.: 1989404