Total 796 qc engineer job vacancies in Quality Assurance / Control category

Our esteemed client in the Manufacturing industry is seeking a QC Technician to join their dynamic team:

• Employment Type: Permanent
• Position: QC Technician
• Location: West (Transport provided from designated pickup point)
• Working Hours: Monday to Friday, 8am to 5.15pm during the first3 months; thereafter, the schedule will change to a 12-hour MORNING shift from 8am to 8.30pm
• Salary Package: Up to $2,900 + Allowances + AWS + Bonus

Job Responsibilities:

• Conduct daily Quality Control (QC) testing for raw materials, in-process manufacturing, and recurring inspections.
• Assist in root cause analysis for product complaints and production rejects, review records, and conduct stability studies.
• Support supervisors in meeting Quality Assurance (QA) targets, such as First-Time Right (FTR) and performance indices.
• Assist in upholding ISO 9001 standards, managing documentation, conducting internal audits, and ensuring good laboratory practices.

Job Requirements:

• Minimum a Nitec in a Chemical-related discipline.
• Prior QC experience within a chemical manufacturing environment is highly preferred.
• Possess prior experience in operating lab equipment such as Gas Chromatographs, Differential Scanning Calorimeters, Autotitrators, and Karl Fischer Titrators.
• Comfortable working on a 12-hour rotating shift schedule.

Ready to apply? Here’s how: 

• Click the APPLY button, or 
• Email your resume (in MS Word or PDF format) to adelin@intuitrecruitment.com. Include the job title in your email subject line for prompt processing. 

Only shortlisted candidates will be notified. 

By submitting your application, you consent to the collection and use of your personal data under Personal Data Protection Act (PDPA). 

Adelin Chong | EA Personnel Reg No.: R1875641 

Intuit Recruitment Pte Ltd | EA License No.: 25C2793 

Overview:
The Quality Control (QC) Technician ensures that products meet quality standards before shipment. This role involves visual and functional inspections, documentation, and communication with production and engineering teams.

Key Responsibilities:

• Perform visual inspections on mechanical and electronic components
• Conduct functional tests using standard testing equipment
• Troubleshoot test equipment problems and perform minor repairs
• Meet daily production QC targets
• Document findings and report non-conformities
• Work with Engineering to understand specifications and tolerances
• Support continuous improvement efforts in quality and process control
• Ensure compliance with internal and regulatory standards
• Maintain cleanliness and organization in the work area

Requirements:

• Technical education or certification in electronics/mechanics (IPC, OSHA, SMTA cert preferred)
• 1–3 years of experience in a QC role in a manufacturing environment
• Familiarity with testing tools and quality procedures
• Strong documentation and communication skills
• Good English (reading/writing technical material)
• Able to see/identify small components on close-up, clearly

Oversee and manage QA/QC activities for workshop fabrication, structural steel works, welding, and site installation.

Conduct inspections to ensure compliance with approved drawings, specifications, codes, and project quality requirements.

Perform visual welding inspections and verify compliance with approved WPS, PQR, and relevant standards.

Monitor fabrication activities in the workshop to ensure workmanship and dimensional accuracy meet project requirements.

Manage material receiving inspections, material control, identification, and traceability throughout the fabrication and construction process.

Maintain complete material traceability records, including Mill Test Certificates (MTCs), inspection records, and material tracking documents from procurement to final installation.

Coordinate and witness NDT activities and ensure all inspection and testing requirements are properly executed and documented.

Prepare and maintain quality documentation, inspection reports, material records, NCRs, and project quality dossiers.

Liaise with clients, consultants, subcontractors, suppliers, and project teams on quality-related matters.

Ensure quality requirements are implemented and maintained from project start-up to project handover and completion.

Review Inspection Test Plans (ITP), Method Statements, quality procedures, and related project documentation.

About No deviation

At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation.

We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development – empowering our team members to grow personally and professionally.

Position Overview

The QC Personnel will be responsible for supporting day-to-day Quality Control laboratory activities, including testing, documentation, method validation support, data review, and compliance with GMP requirements. The role requires hands-on experience with laboratory systems such as GLIMS, Veeva, and SAP, as well as experience in analytical method validation activities.

Key Responsibilities

• Perform routine QC testing for raw materials, intermediates, finished products, stability samples, and/or environmental monitoring samples, as applicable
• Execute laboratory testing in accordance with approved SOPs, test methods, specifications, and GMP requirements.
• Ensure all laboratory activities are completed accurately, timely, and in compliance with data integrity expectations.
• Support sample receipt, testing coordination, result entry, and laboratory documentation.
• Support analytical method validation, verification, transfer, and qualification activities.
  
• Execute validation protocols and document results in accordance with approved acceptance criteria.
  
• Assist in the preparation, review, and closure of method validation protocols, reports, deviations, and supporting documentation.
  
• Support troubleshooting of analytical methods and laboratory investigations where required.
• Use GLIMS for sample management, test assignment, result entry, and laboratory workflow tracking.
• Use Veeva for document management, SOP retrieval, document review, training, and quality records where applicable.
• Use SAP for material/sample-related transactions, inventory checks, batch information retrieval, or quality-related processes.
• Ensure proper documentation practices in line with ALCOA+ principles and GMP expectations.
• Support laboratory investigations, OOS/OOT investigations, deviations, CAPA, and change control activities.
• Ensure timely escalation of abnormal results, laboratory issues, equipment issues, or documentation discrepancies.
• Participate in internal audits, external inspections, and laboratory readiness activities.
• Maintain laboratory areas, equipment, reagents, standards, and records in an inspection-ready state
• Support calibration, maintenance, and qualification readiness of laboratory equipment.
• Assist in laboratory process improvements, system updates, and workflow optimization.
• Work closely with QA, Manufacturing, MSAT, Validation, and Supply Chain teams to support product release and compliance requirements.

Required Qualifications

• Diploma or Degree in Chemistry, Pharmaceutical Science, Biotechnology, Microbiology, Life Sciences, or related discipline.
• Minimum 2 to 5 years of QC laboratory experience in a pharmaceutical, biologics, medical device, or GMP-regulated environment.
• Experience with method validation, method verification, or method transfer is required.
• Hands-on experience with laboratory or quality systems such as GLIMS, Veeva, and SAP.
  
• Experience in QC testing, laboratory documentation, investigations, and GMP compliance.
• Familiar with GMP, GDP, data integrity, ALCOA+, and laboratory compliance requirements.
• Experience with analytical techniques such as HPLC, GC, UV, pH, conductivity, TOC, endotoxin, bioburden, sterility, or other QC methods will be advantageous.
• Able to execute and document method validation activities according to approved protocols.
• Comfortable working with electronic systems for sample tracking, document control, training, and material/batch-related transactions.

Why join us?

• Generous Leave Policy.
• Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
• Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company.
• Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated.
• Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.

How to apply

Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team!

Please submit your resume, outlining your qualifications and experience relevant to the role, here.

Oversee and manage QA/QC activities for workshopfabrication, structural steel works, welding, and site installation.

Conduct inspections to ensure compliance with approveddrawings, specifications, codes, and project quality requirements.

Perform visual welding inspections and verify compliancewith approved WPS, PQR, and relevant standards.

Monitor fabrication activities in the workshop to ensureworkmanship and dimensional accuracy meet project requirements.

Manage material receiving inspections, material control,identification, and traceability throughout the fabrication and constructionprocess.

Maintain complete material traceability records, includingMill Test Certificates (MTCs), inspection records, and material trackingdocuments from procurement to final installation.

Coordinate and witness NDT activities and ensure allinspection and testing requirements are properly executed and documented.

Prepare and maintain quality documentation, inspectionreports, material records, NCRs, and project quality dossiers.

Liaise with clients, consultants, subcontractors, suppliers,and project teams on quality-related matters.

Ensure quality requirements are implemented and maintainedfrom project start-up to project handover and completion.

Review Inspection Test Plans (ITP), Method Statements,quality procedures, and related project documentation

Job Description

• Industry/ Organization Type: Engineering
• Position Title: QC Technician
• Working Location: Tampines
• Working Hours: 5.5 days (Mon to Fri 9AM – 7PM, Sat 9AM – 1PM)
• Salary Package: Basic Salary up to $2,200 + AWS + Bonus
• Duration: Permanent

Key Responsibilities

• Perform in-process, final, and incoming inspections of precision parts using measurement tools such as calipers, micrometers, height gauges, and CMM machines.
• Carry out dimensional and visual inspections to ensure products conform to engineering drawings and customer specifications.
• Record inspection results accurately on quality forms and maintain proper documentation for traceability and audits.
• Detect and report non-conformities or defects, and assist in root cause analysis and corrective actions.
• Ensure adherence to quality procedures, work instructions, and safety standards throughout the production process.
• Any other ad-hoc duties as assigned

APPLY NOW!!!

• Minimum 1 year working experience in related field
• Candidates with Mechanical Engineering background are preferred

Kindly apply through ANY of the following methods:

• Submit your application by clicking the APPLY button;
• Email your resume to Job@anradus.com.sg. Please indicate #77167 on the email subject.

Anradus Application Policy: We value each application and ensure every resume is reviewed. Our process is efficient, typically concluding within 3 working days. If you do not receive communication from us within this timeframe, it's likely that your application has not been shortlisted by our client. In such cases, we recommend continuing your job search to maximize your opportunities.

Anradus Pte Ltd | EA License No. 20C0161 | Rachael Lee | EA Reg No.: R2093131

Job Description

• Industry/ Organization Type: Manufacturer – Dairy Products
• Position Title: QC Technician
• Working Location: Tuas
• Working Hours: 5 days (Mon to Fri: 8:00am – 8.00pm)
• Salary Package: Basic + OT + Performance Bonus, (Gross $3000 - $3500)
• Duration: Permanent

Key Responsibilities

• Conduct sensory checks on raw materials and finished goods, including flavour, odour, and colour.
• Perform solubility testing for applicable products.
• Ensure all LOT testing is completed before product release or lab submission.
• Record test results accurately and report any quality issues promptly.
• Ensure QC/QA approval is completed for all test results.
• Support the preparation and implementation of lab SOPs.
• Prepare, submit, and track samples sent to external labs, including Setsco.
• Review, verify, and file external lab test results.
• Assist with trial samples, customer samples, reference samples, and retention samples.
• Ensure proper sample labelling, traceability, and storage.
• Conduct start-up, changeover, and routine production quality checks.
• Perform hygiene, GMP, environmental, and hand swab checks.
• Handle product changeover, first-off checks, rejection procedures, and related records.
• Review production records, work orders, and data logger results.
• Maintain accurate lab testing, billing, and traceability records.
• Ensure compliance with GMP, HACCP, food safety standards, and internal SOPs.
• Maintain lab cleanliness, equipment, and consumables stock.
• Perform other duties as assigned by the QA Manager or Management.

APPLY NOW!!!

• 3 to 5 years of QC or laboratory experience in food manufacturing is preferred.
• Experience in sensory evaluation and laboratory testing will be an advantage.
• Good knowledge of GMP, HACCP, and food safety systems.
• ISO 22000 and Food Safety Level 1 & 3 certification will be an advantage.
• Able to work in production or warehouse environments and handle physical tasks.
• Able to work 12-hour rotating day and night shifts.
• Proficient in Microsoft Office.

Kindly apply through ANY of the following methods:

• Submit your application by clicking the APPLY button;
• Email your resume to Job@anradus.com.sg. Please indicate #82057 on the email subject.

Anradus Application Policy: We value each application and ensure every resume is reviewed. Our process is efficient, typically concluding within 3 working days. If you do not receive communication from us within this timeframe, it's likely that your application has not been shortlisted by our client. In such cases, we recommend continuing your job search to maximize your opportunities.

Anradus Pte Ltd | EA License No. 20C0161 | Angel Lim | EA Reg No.: R1769781

Location: Tuas
Salary: $2500 Max + $200 Transport allowance + 1 Month completion bonus
Duration: 12 Months

Working Hours:
- 5-day work week
- Mon - Thurs (8am-5pm)
- Fri (8am-3.30pm)

Job Description:
Reporting to the department owner, you will assist in the day-to-day operations of the Quality Control Department to ensure quality is achieved and maintained.
- Support in daily operations of the Quality Control lab
- Preparation of daily olfactive session for incoming raw materials and finished products.
- Keep daily record and appropriate documentation on all laboratory work performed.
- Support in routine analytical testing.
- Ensure compliance to SHE policy and procedure.
- Ensure adherence to company policies and regulations, including LSRs, GMP, ISO9001, ISO14001, ISO45001, and workplace safety protocols.

Job Requirements:
- Min. Diploma/Degree in Food Science, Chemistry, Biology, Microbiology, Biochemistry, or any other relevant field.
- Adapt well to fast paced environment.
- Familiar with standard GLP and Lab Documentation=


If interested, please send updated resume via email  jacelynchua@recruitexpress.com.sg 

Melissa Zhang Zhiqi (Mezzo)

(CEI.No: R2197564 | Recruit Express Pte Ltd (Healthcare & Life Science) | 99C4599)

jacelynchua@recruitexpress.com.sg

Job Description

• Industry/ Organization Type: Precision Manufacturing
• Position Title: QC Technician
• Working Location: Loyang
• Working Hours: 5 days (Mon - Fri, 8.00am - 5.45pm)
• Salary Package: Basic salary up to $2,000 + Performance Bonus
• Duration: Permanent Role

Key Responsibilities

• Prepare and submit first article samples for approval.
• Create packaging specifications.
• Develop inspection plans for products.
• Support inspection processes for in-process, incoming, and outgoing parts.
• Train inspectors and operators on quality check points and measurement methods.
• Work with Production, Toolroom, and Suppliers to address quality issues.
• Ensure documents and records comply with ISO quality standards.
• Assist Engineers as needed.
• Manage and maintain all measuring and testing equipment.
• Help Engineers update monthly quality control reports, such as supplier performance.
• Assist Engineers or Managers in collecting and compiling data for reports.
• Support other quality-related tasks as required.

APPLY NOW!!!

• Minimum 2 years of relevant experience.
• Able to read engineering drawings.
• Good reporting and administrative skills.
• Able to work independently with minimal supervision.
• Experience with OGP Smartscope, CMM, or other measuring tools.

Kindly apply through ANY of the following methods:

• Submit your application by clicking the APPLY button;
• Email your resume to Job@anradus.com.sg. Please indicate #75340 on the email subject.

Anradus Application Policy: We value each application and ensure every resume is reviewed. Our process is efficient, typically concluding within 3 working days. If you do not receive communication from us within this timeframe, it's likely that your application has not been shortlisted by our client. In such cases, we recommend continuing your job search to maximize your opportunities.

Anradus Pte Ltd | EA License No. 20C0161 | Angel Lim | EA Reg No.: R1769781

Our client is one of the leading players in the Medical Industry. Due to business needs, they are now recruiting a Chemist to be part of their team for ongoing transformation projects. They are located in the West.

Responsibilities of Chemist:

• Lead and implement technical testing methods to ensure compliance with regulatory standards for medical device and pharmaceutical products, including those outlined in USP, for markets in the US, EU, and China.
• Supervise a team of chemists across R&D, Technology Transfer, and Projects, emphasizing experience in Product Development and the ability to deliver cost-effective, reliable technologies for sterile medical device production, ophthalmic solutions, and related products.
• Lead technology transfers and projects, ensuring smooth transitions from lab-scale research to R&D scale and eventually to plant scale.
• Develop and optimize testing methods for new materials and finished products to meet regulatory standards.
• Identify and select chemicals that enhance product shelf-life.
• Provide guidance to the QC team on good laboratory practices, equipment handling, and result interpretation.
• Spearhead the development of new chemicals and oversee their technology transfer.

Requirements:

• Minimum Degree in Chemistry or other relevant field of studies
• Minimum 1-2 years of relevant working experience in relevant industry (ISO13485)

Interested candidates who wish to apply for the advertised position, please click APPLY NOW or email an updated copy of your resume/cv.
We regret that only shortlisted candidate will be notified.

Email: Jobs@recruitpedia.sg

EA License No: 19C9682
EA Personnel No: R2198636
EA Personnel Name: Oh Puey Xin

Are you a detail-driven science graduate looking to build a meaningful career in quality assurance? Here's your chance to join a reputable multinational chemical company on Jurong Island — where your analytical skills will directly impact product quality, safety, and operational excellence.

Role Details

• Remuneration Package: Up to $4,000 + Monthly Allowances $1,000 (Experienced Candidates)

• Annual Bonus: AWS + Company Variable and Performance Bonus

• Location: Jurong Island (company transport provided to/from Jurong Island)

• Employment Type: Permanent, Full-Time

• Shift: 12-Hour Rotating Shifts

• Career Growth: Structured development within a global MNC

Key Responsibilities:

As a QC Analyst, you'll be at the heart of laboratory operations — ensuring every product that leaves the facility meets the highest quality and safety benchmarks.

• Conduct routine and non-routine QC analysis on raw materials, in-process samples, and finished products

• Interpret QC results and make sound, independent decisions to support process control

• Collaborate with cross-functional teams to uphold compliance with quality standards

• Take full ownership of the QC laboratory outside of regular hours

• Lead short-term projects including non-routine analysis and customer complaint investigations

• Maintain calibration records and ensure all lab equipment is in optimal condition

• Communicate results accurately and promptly to relevant departments

• Mentor and guide new team members

Key Requirements:

• Degree in Chemistry or a related discipline

• Minimum 2 years of QC experience within laboratory environment

• Familiarity with quality management systems and laboratory techniques

• Strong analytical mindset with sharp attention to detail

• Comfortable working independently in a fast-paced, shift-based environment

• Good verbal and written communication skills

Ready to Take the Next Step?

Submit your CV in MS Word format to connie@triton-ai.com

We regret that only shortlisted candidates will be notified.

Reg No. R1875181| Triton AI Pte Ltd | Licence No. 21C0661

Primary Goals/Objectives:

To provide an effective testing and analytical service to the plant ensuring that products manufactured are tested to specification on time and plant quality and safety goals are met.

Ensure that all raw material, in-process and finished product testing and method transfer testing is carried out per schedule and per GMP. Ensure that records are maintained to appropriate requirements.

Major Responsibilities:

• Perform biochemistry, analytical and raw material of in-process and marketed products for lot release in accordance with quality standards and procedures.
• Responsible for housekeeping duties in the lab. Perform Quality Tag Out for laboratory equipment such as freezer, water bath and etc.
• Support laboratory operations including but not limited to method transfer, equipment qualification, calibration, cleaning and maintenance, purchase and receipt of reagents and consumables, waste management, reagent and media preparation, critical reagent management and document management.
• Review lot release data, identify testing discrepancies and participate in laboratory investigations.
• Participate in inspection and ensure that the laboratory and documents are in a constant state of regulatory compliance and inspection readiness.
• To assist in writing SOP documents, Change plan or change records (document revisions) supporting continuous improvement of test procedures and assay sheet design.
• To carry out completion and review of GMP Documentation of data sheets or LIMS software.
• To carry out QC sample receipt, assay and release procedures.
• Support Audit preparation and any audit related activity
• Reading and understanding the test procedure and the requirements per USP, JP and EP.

Requirements:

• min. Bachelor Degree in Biochemistry and above
• Possess 2-3 years of prior lab analyst experience in bio-chemistry related functions
• Able to do 12 hour rotating day and night shift

Interested candidates, please forward your resume to jalenetan@recruitexpress.com.sg

Consultant: Jalene Tan (R26160390)
Recruit Express Pte Ltd (99C4599)

• Ensure finished goods comply with customer-specified drawing specifications.
• Conduct quality inspections for incoming and outgoing deliveries to verify conformance to specifications.
• Perform dimensional, functional, and other tests using designated measuring equipment, test tools, or checklists.
• Monitor and ensure timely fulfillment of scheduled deliveries.
• Identify and isolate defective products, reporting and highlighting any variances or defects.
• Conduct continuous in-process quality control checks on warehouse floor crates.
• Perform any other ad-hoc duties assigned by the superior.

We regret only shortlisted candidates will be contacted. All applications will be handled confidentially. By submitting your application, you agree to the collection, use, retention, and disclosure of your personal information to prospective employers.

Wecruit Pte Ltd

EA License No: 20C0270

Job Title: In-Process QC Checker (East / AWS + VB)
Job Location: East
Job Hours: 5 days, 8.30am to 6pm

The Opportunity:

• Our client is an established supplements and manufacturing organization that provides an extensive range of products and services to both local and global companies within the health & wellness sector
• Suitable for candidates with production, inspection or QC-checking experience
• Opportunity to learn quality control procedures in a GMP /HACCP factory setting
• Good fit for candidates who are careful, responsible and comfortable with routine checks

Job Responsibilities:

• Perform in-process quality checks during production
• Check product appearance, weight, quantity, sealing, labelling and packaging condition
• Conduct routine inspection based on production schedule and QC requirements
• Record inspection results accurately in QC checklists or production records
• Identify and report defects, abnormalities or non-conforming products to supervisor
• Ensure products are checked according to SOPs and quality standards
• Assist in basic sampling of products or materials when required
• Monitor cleanliness and hygiene practices at the production area
• Support basic finished product checks before packing or release
• Work closely with production operators and supervisors on quality-related matters
• Maintain cleanliness of QC checking area and tools
• Follow GMP, HACCP, hygiene and workplace safety requirements

Job Requirements:

• ITE Nitec / Diploma in any discipline
• No specific food science or pharmaceutical qualification required
• Prior experience in QC checking, production inspection, manufacturing or factory work will be an advantage
• Candidates without QC experience but with good attitude and willingness to learn may be considered

Please submit your updated resume in Word format by clicking the “Apply Now” button or alternatively you can email your resume to Darren.wong(at)cosmosrecruit.com

We regret that only shortlisted candidates will be notified.

Darren Wong Shin Loong
Cosmos Recruit Pte Ltd
www.cosmosrecruit.com
EA License Number: 22C1269
EA Personnel Reg Number: R1985061

Primary Goals/Objectives:

To provide an effective testing and analytical service to the plant ensuring that products manufactured are tested to specification on time and plant quality and safety goals are met.

Ensure that all raw material, in-process and finished product testing and method transfer testing is carried out per schedule and per GMP. Ensure that records are maintained to appropriate requirements.

Major Responsibilities:

• Perform biochemistry, analytical and raw material of in-process and marketed products for lot release in accordance with quality standards and procedures.
• Responsible for housekeeping duties in the lab. Perform Quality Tag Out for laboratory equipment such as freezer, water bath and etc.
• Support laboratory operations including but not limited to method transfer, equipment qualification, calibration, cleaning and maintenance, purchase and receipt of reagents and consumables, waste management, reagent and media preparation, critical reagent management and document management.
• Review lot release data, identify testing discrepancies and participate in laboratory investigations.
• Participate in inspection and ensure that the laboratory and documents are in a constant state of regulatory compliance and inspection readiness.
• To assist in writing SOP documents, Change plan or change records (document revisions) supporting continuous improvement of test procedures and assay sheet design.
• To carry out completion and review of GMP Documentation of data sheets or LIMS software.
• To carry out QC sample receipt, assay and release procedures.
• Support Audit preparation and any audit related activity
• Reading and understanding the test procedure and the requirements per USP, JP and EP.

Requirements:

• min. Bachelor Degree in Biochemistry and above
• Possess 2-3 years of prior lab analyst experience in bio-chemistry related functions
• Able to do 12 hour rotating day and night shift

Interested candidates, please forward your resume to jalenetan@recruitexpress.com.sg

Consultant: Jalene Tan (R26160390)
Recruit Express Pte Ltd (99C4599)