Total 716 Quality Assurance / Control job vacancies

Quality Control Inspector (Beauty & Wellness Products) | 5 Days

Location: East Singapore
Salary: SGD 2,500 – SGD 3,000
Working Hours: Monday to Friday, Office Hours

About the Role

Our client is a reputable logistics and distribution company specializing in beauty, skincare, cosmetics, and wellness products. They are seeking a detail-oriented Quality Control Inspector to ensure products meet quality standards before distribution to customers and retail channels.

Key Responsibilities

• Conduct visual inspections on incoming and outgoing beauty, skincare, cosmetic, and wellness products.

• Verify product packaging, labeling, batch numbers, expiry dates, and product appearance.

• Check products for defects, damages, leakage, contamination, or discrepancies.

• Ensure products comply with quality standards, company requirements, and regulatory guidelines.

• Prepare inspection reports and document any quality issues identified.

• Coordinate with warehouse, operations, and customer service teams on quality-related matters.

• Support product quarantine, rejection, and corrective action processes when required.

• Maintain accurate inspection records and quality documentation.

• Ensure proper handling and storage of products to maintain product integrity.

Requirements

• Minimum GCE N/O Level, NITEC, or Diploma in any discipline.

• Prior experience in Quality Control, Quality Assurance, Product Inspection, Warehouse Operations, FMCG, Cosmetics, Beauty, Pharmaceutical, or Consumer Products industries will be advantageous.

• Good attention to detail with a strong sense of responsibility.

• Basic computer skills and ability to prepare simple reports.

• Able to work independently and follow inspection procedures.

• Familiarity with beauty, skincare, cosmetic, or wellness products will be a plus.

Why Join

• Stable 5-day work week.

• Opportunity to work with established beauty and wellness brands.

• Supportive working environment.

• Training and career development opportunities.

Interested candidates are invited to submit their updated resume to ivytan@jobally.com.sg for consideration.

EA Licence No: 18C9228

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

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

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

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

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)

Job Responsibilities

• Verify incoming electronic components against purchase orders and customer requirements.

• Perform quality inspections according to customer specifications and datasheet requirements.

• Receive, stock, and organize incoming inventory.

• Input and maintain product information within the receiving system.

• Identify, document, and process non-conforming products in accordance with quality management procedures.

• Label conforming products according to customer packaging requirements.

• Prepare and complete inspection reports accurately.

• Resolve discrepancies relating to incoming products and documentation.

• Pull and prepare stock for shipping activities.

• Support quality assurance processes and continuous improvement initiatives.

• Adhere to workplace health, safety, and quality standards.

Requirements

• Minimum 2 years of inspection experience, preferably within the electronics or electronic components industry.
• Experience working in a computer-based operational environment.
• Proficient in Microsoft Word and Excel.
• Basic understanding of electronic components, processors, keyboards, and related hardware is advantageous.
• Strong attention to detail with a commitment to accuracy and quality.
• Able to work effectively in a fast-paced environment.
• Good verbal and written communication skills in English.
• Ability to follow established quality, safety, and operational procedures.

We regret that only shortlisted candidates will be notified.

By sending us your personal data and/or resume, you are deemed to consent to Recruit Fast Pte Ltd or its agents to collect, use and disclose your personal data and/or resume for the purpose of processing and administrating this job application.

Sharmaine Yoong

Recruit Fast Pte. Ltd. (EA License: 23C1828)

EA Personnel: R24124011

Company Overview

Poli Medical Company Pte Ltd is a Singapore-based pharmaceutical manufacturer with an HSA-certified GMP facility. Established in 1971, it specializes in natural herbal supplements, contract manufacturing, and distribution of health and food supplements under the TruLife brand.

Job Summary

A Quality Control Executive inspects, tests, and samples materials and products to detect defects and deviations from specifications. You will monitor production operations, review documentation, and recommend corrective actions to ensure product safety and quality compliance.

Responsibilities

• Inspect materials, parts, and products on the production floor and in the warehouse to identify defects and deviations from specifications
• Conduct incoming inspections and accurately record inspection results for traceability
• Assist the Quality Team with daily inspection activities, including monitoring temperature and humidity controls to maintain product integrity
• Review and verify production documentation such as batch records to ensure compliance with quality standards
• Perform quality assurance inspections on incoming and outgoing goods to maintain product quality
• Monitor production quality by recording inspection and test results, identifying trends, and recommending process adjustments to prevent defects
• Communicate inspection findings clearly and collaborate with production teams to implement corrective actions promptly

Required competencies and certifications

• Diploma or Degree in Food Science, Food Technology, or related disciplines

Preferred competencies and qualifications

• Strong analytical and problem-solving skills applied to quality control processes
• Excellent interpersonal and communication skills for effective reporting and teamwork

QC Validation Specialist (Equipment Qualification/ Pharma/ Contract)

Duration: 6 months

Location: Tuas   

Salary : Up to $10,000 depending on experience

Our client is a US healthcare and a leading global biopharmaceutical company. They have more than 69,000 employees across 140 countries with a heritage of more than 125 years. Our client is committed to provide patients and customers with a reliable supply of high-quality, safe, and effective medicines and vaccines. Their global supply strategy relies on manufacturing capabilities and expertise to achieve this mission

Responsibilities

• Perform/review system qualification, requalification, relocation, decommissioning and retirement for laboratory equipment in accordance with approved procedures and standard lead time.
• Assume role of Subject-Matter-Expert of laboratory system lifecycle, collaborates closely with cross-functional teams and above-site functions. This includes initiating alignments proactively, sharing expertise, and providing input to ensure alignment and consistency across the organization.
• Author/review Quality Notifications and Test Exception Reports, lead root cause analysis and ensure effective implementation of related actions within the agreed timeframe. 
• Conduct troubleshooting of laboratory system lifecycle, identifying and resolving any issues that may impact the business/work efficiency and compliance.
• Identify opportunities and propose solutions to improve efficiency and compliance in processes, standards, and best practices within the team.
• Provide leadership, expert guidance and support to team members, acting as a go-to resource for problem-solving and decision-making.   
• Provide skills training to other team members, ensuring they have the necessary knowledge and competencies to perform their duties effectively.
• Any other duties as assigned by reporting manager.

Requirements:

• Diploma or bachelor’s degree in chemical engineering or any other relevant engineering field
• At least 5 years of experience in qualification, requalification, relocation, decommissioning and retirement of Good Manufacturing Practice (GMP) Lab equipment (not limited to Ultraviolet–Visible (UV-Vis) Spectrometer, Total Organic Carbon (TOC) Analyzer, Microplate Reader, Liquid Particle Counter, Capillary Electrophoresis (CE), High-Performance Liquid Chromatography (HPLC), Analytical Balances, Incubators, Particle Counters)
• Experience in GMP environment within the pharmaceutical/chemical manufacturing.

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

Recruitment Consultant (R2090579)

Manpower Staffing Services (S) Pte Ltd

EA Licence: 02C3423

Working Hours

12 hour rotating day and night shift

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 equipments 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.

Qualifications:

• Bachelor of Science majoring in Chemistry, Biochemistry or related scientific degree

• At least 1-3 years relevant experience depending on qualification, preferably in the bio-pharmaceutical / Pharmaceutical industry

• Good working knowledge of cGMP and regulatory requirements related to Quality is preferred

• Knowledge of cGLP / cGMP, FDA, EMA and ICH guidance’s and industry standards for analytical development and characterization.
  

  Interested applicants, please email your updated CV to rachel.lim@recruitexpress.com.sg or WA 97527630 for more information.

  We regret to inform that only shortlisted candidates will be contacted.

  EA Personnel: Lim Ruo Yi, Rachel (R23116144)

  Company EA license No.: Recruit Express Pte Ltd (99C4599)

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
• Office hours are available for Senior roles

Interested candidates please send your updated resume in MS word format to:

kate.leau@recruitexpress.com.sg
Subject: Senior QC Chemist (Bio)


EA Personnel: Kate Leau Wei Xuan (R1552331)
Company Registration No.: 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

1. QC Technician (Monthly Rotation) /Up to $3,500 @Joo Koon

• Morning (7am - 3pm); Afternoon (3pm - 11pm ($8.50/day); Night (11pm - 7am ($14/day)

• Develop and implement quality control processes and procedures

• Inspect, audits, and tests on raw materials, in-process components, and finished products.

• Identify quality issues and non-conformities, implement corrective and preventive actions.

• Utilise SPC techniques to analyse production processes, identify trends, and detect variations.

• Generate & analyse SPC charts and data to assess process stability and make recommendations.

• Ensure compliance with QMS requirements including ISO 9001 standards

• Participate in audits to verify adherence to QMS procedures and standards

• Calibrate measurement and inspection equipment used in quality control activities.

• Maintain records of quality control activities, inspection results, and non-conformities
  

  
  

  Interested applicants, send in your updated resume by clicking “Apply Now”.

  Lin Weikang
  EA Personnel No: R21102570
  EA License No: 23C1894

The QC Technician is responsible to inspects incoming raw materials, electronic, mechanical components as well as manufactured/ OEM products to ensure they meet design specifications before being released to production. Completes appropriate paperwork necessary for conforming and non-conforming materials.

How You’ll Make an Impact:

• Perform inspection or testing of product to ensure conformity to defined specifications, QC checklist and/or drawings.
• Document inspection result and perform system transaction in the SAP after buyoff or inspection.
• Perform inspection and document results of FAI samples submitted from supplier.
• Initiate Quality Notification via SAP for Non-Conforming products detected during inspection
• Carry out any other administrative job function. (eg collating of DHR)

What You Bring:

• Minimum Secondary school/ NITEC/ Diploma in any engineering or related course of studies
• At least 2 years of working experience in manufacturing is preferred.
• Experience in performing inspection of parts, such as PCBA, electrical and mechanical parts with reference to engineering drawing/specification.

• 8:30am - 5:30pm (Monday to Friday)

• Budget: $2500 - $3000

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

Consultant: Huang Jingsheng Kevyn (R1333338)
Recruit Express Pte Ltd (99C4599)

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION:
Join Thermo Fisher Scientific's Quality Assurance team and contribute to our mission to make the world healthier, cleaner and safer. As a Quality Engineer II, you will ensure compliance with quality standards and regulatory requirements across our manufacturing operations. You'll collaborate with cross-functional teams to drive continuous improvement initiatives, lead investigations, and implement corrective actions to maintain our high standards of product quality. This role offers exposure to innovative technologies and the opportunity to directly impact patient care through quality oversight of critical products.

RESPONSIBILITIES

• Retrieve complaints from various database and update complaint log.

• Review and process complaints in a uniform and timely manner.

• Review technical complaint threshold report and initiate escalated complaint(s) from various databased into Trackwise System.

• Lead in the resolution of customer complaint and quality issues on manufacturing floor to provide voice of customers to operations and translate customer's feedback into innovative solutions.

• Identify and establish incoming and outgoing Product QC inspection criteria and provide training to QC Technicians.

• Participate in Product Qualification activities by reviewing test protocols and reports to ensure product quality meet the specified requirements.

• Issue RMA (Return Material Authorization) for units that requires to be returned for FA (Failure Analysis) and ensure it returns for FA.

• Perform failure analysis on product failures and work with Engineering to resolve product faults.

• Establish DMRI (Device Master Record Index).

• Review change orders, deviation and risk management for products.

• Provide management with quality data and trends in product performance in meeting customer requirements.

• Participate in internal audits to ensure the effective implementation of Quality Management System.

• Act as Operation QA Representative for NPI (New Product Introduction) project and Transfer project.

• Act as customer representative, attend to customer enquires/ feedback, assist in customer visit, coordinate, and lead the team in customer audits.

• Lead in quality initiatives program to address system inadequacies which may include quality programs, tracking, analyzing, reporting and problem solving to achieve continual quality improvement objectives.

• Supports company goals and objectives, policies, and procedures in compliance with quality systems, cGMP and FDA regulations.

• Ensure that systems and procedures are in compliance with ISO13485, MDSAP, FDA 21CFR Part 820, IVDR, ISO9001, ISO14001 and ISO45001 requirement.

• Support plant-wide activities and special projects, as assigned.

REQUIREMENTS:

• Advanced Degree with no prior experience, or Bachelor's Degree plus 2 years of quality assurance experience in GMP/ISO regulated environments, preferably in medical devices, pharmaceuticals or biotechnology

• Preferred Fields of Study: Life Sciences, Engineering, Chemistry or related scientific/technical field

• Strong knowledge of quality systems, cGMP regulations, and standards including ISO 13485, 21 CFR Part 820

• Expertise in quality tools and methodologies including risk management, root cause analysis, CAPA, and change control

• Demonstrated experience leading investigations, analyzing quality data, and implementing effective corrective actions

• Excellent documentation and technical writing skills for developing SOPs, Work Instructions and reports

• Strong proficiency in quality management software (TrackWise, SAP QM, etc.) and Microsoft Office suite

• Experience conducting internal audits and supporting external regulatory inspections

• Demonstrated ability to build consensus and collaborate across functions

• Strong verbal and written communication skills

• Ability to work independently while contributing effectively in team environments

• Strong attention to detail with analytical and problem-solving capabilities

• Experience with statistical analysis tools and quality metrics reporting

• Project management skills and ability to prioritize effectively

Test Engineer (Hardware / Equipment)

The Role:

• Perform qualification/buy-off data collection oftest hardware/equipment eg. on changekit / load board/ test handler/ post testscanner based on release criteria.
• Perform Test Hardware In/Out activities includingbut not limited to SA creation, coordination with warehouse team,Incoming/Outgoing QC checks, Packing/Unpacking.
• Ensure that all test hardware is properly labelledand update hardware inventory for any movement and change of status. 
• Perform ESD test measurement on test hardwareand facility as required.
• Ensure that test hardware adheres to 5S requirements.

Job Requirements:

• Degree or Diploma in Electronics Engineering / ElectricalEngineering / Semiconductor Technology with 2 – 4 years of relevant workingexperience in semiconductor testing
• Fresh Degree graduates are welcome to apply
• Proficient in MS Word, MS Excel and MS Powerpoint

Role and Responsibilities

1. Engineering & Design

· Understand customer requirements provided through project kick-off documents such as customer standards, project specifications, basis of designs, sequence of operations, equipment interfacing points lists, schematic drawings and layout plans.

· Work together with equipment suppliers and subcontractors to formulate ACMV control systems solution proposal to meet customer requirements.

· Identify key engineering design and further develop solution proposal into the necessary, material, schematics drawing, layout plans, typical details, control panel designs, system sequence of operation, points list and methods statement technical documents for submission and approval.

· Understand and define testing & commissioning strategies, work with other parties for troubleshooting and solution identification during site implementation.

2. Planning & Coordination

· Consider manpower and resource planning to develop timelines, detail work schedule and implementation plans for ACMV control scope of engineering construction projects.

· Effectively coordinate with cross-functional teams, equipment vendors and sub-contractors to meet project requirements.

· Maintain clear documentation throughout progressive project phases.

3. Compliance & Safety

· Understand, apply and comply to local standards or codes of practice as well as relevant industry standards.

· Understand, execute and ensure site compliance to company directed and project required safety management systems.

4. Stakeholder Communication

· Effectively liaise with and manage external stakeholders such as customers, consultants and main contractors to understand and meet project requirements and fulfil project deliverables.

· Provide project planning and progress updates through the update of project implemented trackers.

· Prepare training and handover materials, operation maintenance manuals.

5. Others

·  All other ad-hoc tasks as assigned by reporting manager.

Qualifications and Education Requirements

· Relevant Qualification in Mechanical/ Electrical/ Mechatronics Engineering or equivalent.

· For experience candidates, preferably to possess minimum 3 years relevant experience in the Industrial Engineering industry.

· Open to candidates with no previous working experience for junior position

·  Outgoing with strong interpersonal and effective communication skills.

·   Ability to work independently and target oriented in a fast-paced environment.

·   Ability to interact effectively with Clients, Consultants, project members and managers at all levels

Working days: 5-day work week 
Working hours: 9am to 6pm
Work location: Boon Lay
Salary: $2300 - $2800

Responsibilities:

• Ensure the food manufacturing process comply with food safety standards, specifications, and government and industry regulations.
• Assist in the implementation and maintenance of ISO 22000, FSSC 22000, Halal and SFA documentation and standards.
• Conduct routine inspections of production processes to ensure compliance with regulatory standards and perform routine in-process checks on products.
• Support regulatory inspection, customer audits and visits and to follow-up with corrective action and documents, when necessary.
• Responsible for reporting any non-conformance of products / process and timely reporting to the Executive / Manager.
• Other ad-hoc duties as required.

Requirements:

• Knows how to use MS Office.
• Able to work in chilly environment (10°C to 15°C).
• Preferably a Diploma in Food Science, Food Technology or equivalent.
• Preferably knowledgeable in local & international food safety standards

The Supreme HR Advisory Pte. Ltd || 14C7279

Chua Jie Ying (Cai Jie Ying), Evelynn || EA Personnel License R24120580

Quality Engineer

Company Overview / Employee Value Proposition

For over 27 years, ACP has led ICT innovation in Singapore, partnering with major government agencies and corporations. As an exclusive distributor in Southeast Asia, ACP drives digital transformation with a skilled team and a legacy of trusted, high-quality technology solutions.

Job Summary
We are seeking a passionate and driven Test Engineer who thrives on complex system integration challenges. In this role, you will go beyond test execution. You will help architect, develop, and automate the testing framework for our next-generation e-payment ecosystem, playing a key role in shaping the future of digital finance.

Responsibilities:

• Responsible for the end-to-end testing activities of an integrated e[1]payment system;
• Carry out the activities in the testing lifecycle including test planning, analyzing business and system requirements;
• Designing and developing the test cases and procedures or test automation solution;
• Preparing the test environment;
• Executing the test procedures;
• Logging and tracking defects to closure; and
• Conducting test reviews with internal and external stakeholders

Qualifications

• Recognised degree or equivalent in Information Technology or Engineering with at least 3 years’ relevant experience in executing testing or developing test automation solution involving devices (UI-based or embedded) and/or back-office systems;
• Possess a strong interest and self-motivation to carry out testing with the objective to contribute towards a better quality software/system;
• Good written and verbal communication skills in English
• Able to work well both independently as well as in a team;
• Familiarity with the full system development lifecycle from requirement, development, to testing and deployment;
• Relevant experience and competence with the tools used for test management, configuration management and defect tracking;
• Familiarity with database administration;
• Certification in software testing;
• Experience in micro-payment or Automatic Fare Collection systems using Smart Card; and
• Skilled in executing testing or developing test automation solution, he/she shall also possess either one of these sets of skills: Either
• i. Good capability in developing effective test cases and procedures from analysing business requirements and system use cases; and
• ii. Competent in executing testing activities (including System Testing, System Integration Testing, User Acceptance Testing) which include preparation of the test environment, test execution, recording of test results, conducting of test reviews with both internal and external stakeholders, to logging of and following up on defects to closure.
• Or/And
• i. Competent and having a keen interest in software development, particularly in the area of test automation;
• ii. Relevant experience and competence with at least one test automation tool, to develop test automation application and scripts; and
• iii. Good capability in developing design documents and user manuals which could effectively describe and provide clear instructions on the test automation solution to the end users who include testers and stakeholders.

Join Velocity Electronics as our next Quality Engineer in Singapore.

If you are driven to elevate quality standards and strengthen operational performance that support business success — we want to meet you.

What can you expect to do?

The Quality Engineer ensures product conforms to our customers’ requirements and assists with responding to customer concerns related to product quality in order to deliver exceptional experiences and outcomes.

You will be responsible for:

• Perform final quality control (QC) checks on inspected product to ensure it conforms to our customers’ requirements
• Provide training and technical support and assist with responding to customer concerns related to product quality
• Conduct internal QMS and ESD audit

In addition, you will:

• Review inspection results and, as needed, perform supplemental inspections on product to determine acceptability of product
• Document results of final QC checks in Velocity’s ERP system
• Communicate inspection findings to the Purchasing and Sales teams and advise on the actions necessary to resolve issues (if applicable)
• Coordinate with the Operations Manager to ensure Inspectors are performing inspections to standard
• Conduct inspection skills and technical trainings for quality inspectors
• Provide technical support to Sales and Purchasing Departments
• Assist the Quality Manager in Customer Corrective Action Request
• Perform other duties as requested by management

What is the experience and knowledge needed to be successful in this role?

Our ideal candidate is:

• Exceptional judgment
• Detail-oriented and thorough
• Strong written and verbal communication skills
• Problem solver
• Able to effectively coordinate and communicate with others
• Adaptable and flexible
• Able to work on several projects simultaneously
• Independent

Skills and Experience:

• Bachelor’s degree preferred; Diploma holders with relevant experience will also be considered
• Minimum 5 years of experience performing quality inspection on electronic components with demonstrated ability to make valid conformance decisions
• Expert product knowledge, experience working with complex ERP systems
• Understanding of basic math, including percentages and tolerances

This position will be located in our Singapore Office, APAC Regional Headquarters.

Please note that applicants must have the legal right to work in Singapore, as visa sponsorship is not available for this role.

Why Join Us

At Velocity Electronics, our core values—Be Amazing Today, Demonstrate Mutual Respect and Trust, Act Courageously, and Own Your Outcomes—drive our success.

If you thrive in a fast-paced, results-oriented environment and are motivated to exceed targets, you will be empowered to take ownership of your success, build meaningful relationships, and drive growth through innovative solutions.

Join a top independent electronic components distributor serving the world’s leading contract manufacturers and OEMs.

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.

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, 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

About You:

• Bachelor of Science majoring in Chemistry, Biochemistry or related scientific degree
• At least 1-3 years relevant experience depending on qualification, preferably in the bio-pharmaceutical / Pharmaceutical industry
• Good working knowledge of cGMP and regulatory requirements related to Quality is preferred 
• Problem-solving and troubleshooting skills
• Highly motivated and independent
• Possess good interpersonal and communication skills
• Knowledge of cGLP / cGMP, FDA, EMA and ICH guidance and industry standards for analytical development and characterization
• Must be able to do rotating 12-hour shift work (day and night shifts)

1 year contract, subject to extension