692 Quality Control jobs in Jurong West

We are looking for a Quality Control (QC) Technician who will be responsible for performing document management, defect analysis, quality inspections, and reporting to ensure product quality and compliance with standards. The role involves coordination with various departments and external partners to maintain high-quality standards across all stages of production and shipment.

• Perform document review, revision, circulation, training, and retention for both hard copy and soft copy; maintain document storage area housekeeping.
• Conduct failure analysis on field return samples and in-process defect samples.
• Arrange test samples for testing at Batam factory, Japan headquarters, and external test labs.
• Perform incoming material quality inspections and liaise with vendors regarding non-conformity issues.
• Conduct finished goods outgoing quality inspections, packaging, and prepare quality documentation for shipment.
• Carry out quality patrol inspections to monitor ongoing quality standards.
• Lead quality-related meetings and disseminate meeting minutes.
• Evaluate new and changed samples for quality, and present findings using PowerPoint.
• Update daily, weekly, and monthly quality reports.
• Communicate with BT factory on special shipment instructions and follow up until issues are resolved.

• NTC (National Trade Certificate) or equivalent diploma/NITEC in relevant fields such as Electronics, Mechanical, Quality Assurance, or related technical disciplines.

• Understanding and practical application of quality management systems and tools such as ISO 9001, SPC (Statistical Process Control), FMEA (Failure Mode and Effects Analysis), FTA (Fault Tree Analysis), and 8D methodology.
• Ability to interpret technical drawings and specifications.
• Proficiency in operating measurement microscopes and other inspection tools.
• Ability to work in a clean room environment, including wearing appropriate protective gear.
• Fluent in English and Chinese (both spoken and written) for effective communication and documentation with shipping vendors across China region.
• At least 1 year of working experience in a similar electronic or manufacturing environment, particularly in quality inspection, defect analysis, or QC-related tasks.
• Open to fresh graduates without prior experience, provided they demonstrate relevant skills and knowledge.

• Open-mindedness and adaptability to job changes.
• Effective communication and presentation skills.
• Willingness to work overtime if required.

• Great exposure to a large MNC
• Hybrid work arrangement
• Medical, Dental & Leave benefits
• Access to the Company Gym and Karaoke room
• Company-sponsored training for professional development
• Work location within walking distance from Bedok MRT
• Work hours: Mon to Fri (8am - 5pm)

Join Panasonic Industry, a company with over 100 years of expertise in device technologies, committed to transforming society by delivering innovative solutions that exceed customer expectations. Be part of a team that drives meaningful, impactful change through advanced technological solutions.

• Responsible for overseeing and implementing quality control processes to ensure the processed metals meet customer expectations and complies with industry standards and regulations.
• Support the Assurance Supervisor in daily operations of maintaining and improving our quality management processes and systems, and ensuring compliance with all quality and safety protocols.

• Perform regular quality assessments on all incoming materials from vendors
• Ensure all finished products to be exported meet the specifications required and complies with industry standards
• Resolve quality-related issues in a timely manner
• Identify areas for process improvement and efficiency in quality control procedures
• Maintain inventory update of materials
• Document inspection outcomes by ensuring all completed detailed reports submitted to management are accurate
• Ensure all equipments are maintained according to SOP and overseeing repairs when not in good running condition
• Ensure the team completes the assigned daily work schedule and production target is achieved
• Ensure all employees follow workplace safety rules

Quality assurance is an essential aspect of our organization. We are seeking a dedicated individual to assume the role of Quality Assurance & Quality Control Assistant in our derma laboratory department based in Singapore.

The primary responsibilities of this position involve maintaining quality standards by approving incoming materials, in-process production, finished products, and recording the results. Additionally, the successful candidate will be responsible for upholding safety regulations and supervising the production process to ensure that all our products meet GMP quality expectations.

Key areas of responsibility include:

· Perform regular quality assessments on all incoming materials from vendors and outgoing products for delivery.

· Manage and qualify products and material quality to meet compliance and industry standards.

· Recommend improvements to the production process to ensure quality control.

· Resolve quality-related issues in a timely manner.

· Maintain QC records.

· Approve all finished products by confirming specifications and conducting required tests.

· Return products for re-work if needed and complete documentation to confirm re-work.

· Document and update inspection results by completing reports and logs.

· Keep measurement equipment operating by following operating instructions and calling for repairs.

· Maintain a safe working environment by adhering to standards and procedures and complying with legal regulations.

· Devise sampling procedures and directions for recording and reporting quality data.

· Plan, conduct, and monitor testing and inspection of materials and products to ensure finished product quality.

· Document internal audits and other quality assurance activities.

· Investigate customer complaints and non-conformance issues.

· Perform related performance testing including stability tests.

The ideal candidate should possess excellent communication and leadership skills, as well as a keen attention to detail. If you are a motivated and organized individual who is passionate about delivering high-quality results, we encourage you to apply.

Join to apply for the Quality Control Specialist role at Cytiva

Join to apply for the Quality Control Specialist role at Cytiva

Direct message the job poster from Cytiva

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.

You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.

Learn about the Danaher Business System which makes everything possible.

The Quality Control Specialist is responsible for ensuring products and processes meet established quality standards and regulatory requirements. This role involves conducting inspections, testing, and audits, as well as supporting continuous improvement initiatives to maintain high levels of product quality and operational efficiency.

This position reports to the Quality Control Manager and is part of the Quality department located in Singapore, 25 Tuas South Street 1 and will be an on-site role.

What you will do:

• Leading/providing oversight in OOS investigation, deviation report writing and CAPA planning
• Provide general oversight on QC routine operations, ensuring that the product and raw material testing schedules are on-track with minimal backlog
• Approximately 30% of time dedicated to performing Quality Control (QC) testing activities, 70% of time focused on supporting various QC operational activities
• Driving adherence to quality KPI’s and ensure timely reporting of data and trend to relevant stakeholders
• Ensure that validation of new QC laboratory equipment and method is performed
  
  

• University graduate (Science) with reasonable work experience OR equivalent relevant work experience
• Possess at least 3 to 5 years of experience working in a QC Laboratory environment
• Extremely detail and accuracy-oriented with good written and verbal communication skills
• Experience in writing Laboratory Investigation details, Deviation records with root cause analysis and Change Control records
• Knowledge and experience of a GxP environment or other regulated industry
  
  

• Computer literate (Word, Excel, Oracle database, Electronic Documentation System) to create spreadsheets, e-mail, memos, graphic, and technical writing skills (create and edit procedures)
• Reasonable laboratory experience operating laboratory equipment, i.e. UPLC, Endotoxin plate readers, pH meters, microbial testing etc.
  
  

• Seniority level Not Applicable

• Employment type Full-time

• Job function Quality Assurance
• Industries Biotechnology Research, Medical Equipment Manufacturing, and Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at Cytiva by 2x

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

Job Duties and Responsibilities

1. Lead a team of QC Executives to provide support on quality systems, processes, and procedures to ensure compliance with FM Contract, Company’s, and ISO policies.

2. Responsible for preparing and conducting quality control checks in a systematic manner, investigations for potential quality non-conformance, compliance concerns and recommend follow-up actions to mitigate such issues.

3. Prepare report for management review and facilitate for follow-up actions required.

4. Supervise and manage contractors, sub-contractors and provide liaising duties with clients to ensure service delivery, ad-hoc works, and all scheduled maintenances are performed on time.

5. Attend regular maintenance meetings on behalf of the Company with Clients and Clients’ Representatives.

6. Lead the internal audit program for operation site include identifying opportunities for quality systems’ improvements and meet company’s quality objectives.

Required Qualifications

1. Minimally Diploma in any Engineering field, Facilities or Estates Management or equivalent, preferably with knowledge in ISO Standards 9001, 14001 and/or 41001.

2. Certified QMS Auditor / Lead Auditor in ISO or equivalent will be advantageous.

3. Pro-active, independent yet service and team-oriented, and able to perform under pressure with minimal supervision.

4. Strong interpersonal and communication skills with ability to work cross-functionally with different departments to meet timeline and objectives.

5. 5.5 work days

6. Location: Tengah Air Base

Job Description

Job Scope & Responsibilities :

• Handle full set of accounts
• Perform monthly financial closing
• Coordinate and liaise with external parties such as auditors, tax agents, and tax authorities
• Manage all duties related to Human Resources
• Prepare monthly payroll and submit CPF contributions
• Handle IRAS AIS, IR8A, corporate tax, income tax, etc.
• Manage MOM WPOL/EPOL matters
• Perform other administrative duties as required
• Undertake any ad hoc duties as assigned

Job Requirements :

• Candidate must possess at least a diploma or equivalent
• Proficiency in both English and Chinese Mandarin (reading, writing, and speaking) is required, as the role involves liaising with Mandarin-speaking associates
• Minimum of 2 years of relevant work experience

Bring more to life.

Are you ready to accelerate your potential and make a real difference within the fields of life sciences, diagnostics, and biotechnology?

At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.

You’ll thrive in a culture of belonging where your unique viewpoint matters. By harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our customers undertake activities ranging from fundamental biological research to developing vaccines, medicines, and cell and gene therapies.

At Cytiva, you will have the opportunity to improve yourself and us—working on meaningful challenges with caring colleagues, customers, and patients. Take your next step toward a life-changing career.

Learn about the Danaher Business System , which makes everything possible.

The Quality Control Specialist is responsible for ensuring products and processes meet quality standards and regulatory requirements. This involves conducting inspections, testing, audits, and supporting continuous improvement initiatives to maintain high product quality and operational efficiency.

This position reports to the Quality Control Manager and is based on-site in Singapore, 25 Tuas South Street 1.

• Leading oversight of OOS investigations, deviation report writing, and CAPA planning.
• Monitoring QC routine operations to ensure testing schedules for products and raw materials are on track with minimal backlog.
• Approximately 30% of time dedicated to performing QC testing activities; 70% supporting QC operational activities.
• Driving adherence to quality KPIs and ensuring timely data reporting and trend analysis.
• Validating new QC laboratory equipment and methods.

• University graduate in Science or equivalent relevant experience.
• 3 to 5 years of experience in a QC Laboratory environment.
• Detail-oriented with strong written and verbal communication skills.
• Experience in laboratory investigations, deviation records, root cause analysis, and change control.
• Knowledge of GxP or similar regulated environments.

• Proficiency with Word, Excel, Oracle, and electronic documentation systems.
• Laboratory experience with equipment such as UPLC, endotoxin readers, pH meters, and microbial testing.

#LI-SS3 #LI-Onsite

Join our team today. Together, we’ll accelerate the impact of science and technology. We partner globally to solve complex challenges and bring science to life.

For more information, visit .

At Danaher, we value diversity and believe in the power of different perspectives, both visible and not, in our workforce and markets.

Join to apply for the Quality Control Inspector role at Weatherford .

Job Description

Under direct supervision, assists with monitoring, testing, and inspecting all processes involved in the production of a product and the product itself. Ensures that quality standards are met for every component of the product or service provided by the company.

Responsibilities

• Inspect products using established inspection tools and techniques.
• Perform and document First Article, In-Process, and Final inspections to ensure customer requirements and quality standards are met.
• Inspect materials and products received from outside sources for compliance with quality standards and customer specifications.
• Complete all assigned technical and safety trainings timely.
• Work in the field (outdoor conditions), assisting with material movements for inspection.
• Clean drilling tools and rig equipment for inspection.
• Maintain cleaning machinery, including mechanical brushing units, steam cleaners, and high-pressure jetting equipment.
• Ensure safety and environmental control over cleaning machinery and work areas.
• Report unsafe conditions or acts to the supervisor.
• Perform work in accordance with approved plans, schedules, and programs.
• Operate equipment and fixed assets responsibly and correctly.
• Apply Weatherford and client company Quality, Health, Safety & Environment policies and systems.
• Follow all safety rules and company policies.
• Carry out work assignments to the highest quality standards.
• Perform other duties as assigned by the supervisor within the physical constraints of the job.

Qualifications

• Secondary school graduation or technical education is a plus.
• At least 3 years of related QC inspection experience.
• Good verbal and written communication skills in English.
• Knowledge of products and inspection processes.
• Ability to use measurement devices such as tape measures, micrometers, callipers, and scales.
• Ability to read and understand blueprints and charts.
• Effective teamwork skills.
• Physical ability to respond to emergency situations immediately.

• Mid-Senior level

• Full-time

• Quality Assurance

• Oil and Gas

Join to apply for the Quality Control Specialist role at myGwork - LGBTQ+ Business Community

1 day ago Be among the first 25 applicants

Join to apply for the Quality Control Specialist role at myGwork - LGBTQ+ Business Community

Get AI-powered advice on this job and more exclusive features.

This job is with Danaher, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.

You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.

Learn about the Danaher Business System which makes everything possible.

The Quality Control Specialist is responsible for managing a team of QC associates and ensuring that QC routine operations are carried out as per plan.

This position reports to the Quality Control Manager and is part of the Quality department located in Singapore, 25 Tuas South Street 1 and will be an on-site role.

What You Will Do

• Leading/providing oversight in OOS investigation, deviation report writing and CAPA planning
• Provide general oversight on QC routine operations, ensuring that the product and raw material testing schedules are on-track with minimal backlog
• Driving adherence to quality KPI's and ensure timely reporting of data and trend to relevant stakeholders
• Ensure that validation of new QC laboratory equipment and method is performed
• Developing and maintaining specialized technical expertise in order to provide support for existing products and ongoing GxP operations as required
  
  

• University graduate (Science) with reasonable work experience OR equivalent relevant work experience
• Possess at least 3 to 5 years of experience working in a QC Laboratory environment
• Extremely detail and accuracy-oriented with good written and verbal communication skills
• Experience in writing Laboratory Investigation details, Deviation records with root cause analysis and Change Control records
• Knowledge and experience of a GxP environment or other regulated industry
  
  

• Computer literate (Word, Excel, Oracle database, Electronic Documentation System) to create spreadsheets, e-mail, memos, graphic, and technical writing skills (create and edit procedures)
• Reasonable laboratory experience operating laboratory equipment, i.e. UPLC, Endotoxin plate readers, pH meters, microbial testing etc.
  
  

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Quality Assurance
• Industries Medical Device

Referrals increase your chances of interviewing at myGwork - LGBTQ+ Business Community by 2x

Johor Bahru, Johore, Malaysia 10 hours ago

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.