239 Quality Control jobs in Tuas

QUALITY CONTROL INSPECTOR

The main duties of the job will be to:

Responsibilities

1. Perform assigned inspection and test activities across Wilhelm group facilities.
2. Perform applicable incoming, in-process and final inspection as per quality plan
3. Operate Coordinate Measuring Machine and Faro Arm equipment
4. Verifying compliance with applicable test specifications, codes, standards and customer specification
5. Prepare and submit required quality report(s), certification or documentation
6. Ensure clear identification of product inspection status

Requirements

• Good diploma in Engineering or equivalent
• Possess minimally UT/MPI/DPI ASNT or PCN NDT Level II certification
• Minimum 2 years of QAQC work experience
• Proficient in reading drawings/blueprints
• Previous experience in and/or familiarity with the oil & gas industry preferred

If you are shortlisted for the position(s), you should hear from us within 30 days of the closing date of the advertisement.

• Handle callers' enquiry, orders or complaints
• Processing order received from telephone or emails etc
• Prepare work/production order to Production /Lab
• Prepare Delivery orders and Invoices.
• Ensure all Delivery orders are given to the delivery driver on time
• Compile and data input of all daily ink production Sales /BOM into SAP System
• Prepare quotations for local customers
• Support Sales and Marketing team on phone sales calls and appointment/travel arrangement
• Assist in updating monthly stock inventory and data entry for accounts
• Preparation of Technical Data sheet and support Lab on Quality control on incoming materials
• Preparation of Import and Export shipping documents

COMPANY OVERVIEW:

At Alcon, we are inspired by the meaningful work we do to help people see brilliantly. As the global leader in eye care, we boldly innovate, champion progress, and act with speed. We recognize and celebrate the contributions of our people, offering career opportunities that empower growth and fulfillment. Together, we go above and beyond to make a lasting impact on the lives of our patients and customers. We cultivate an inclusive culture and invite diverse, talented individuals to join us in shaping the future of eye care.

ROLE SUMMARY:

As a Technician II, Quality Control Lab – Chemistry, you will play a key role in supporting manufacturing operations by performing chemical analyses, maintaining laboratory equipment, and ensuring compliance with regulatory standards. This is an excellent opportunity for individuals passionate about laboratory work and quality assurance in a dynamic, regulated environment.

In this role, a typical day will include:

• Perform testing and/or inspection on raw material, in-process material, finished products and monitoring activities.
• Review/Approve testing documentation and test records. Maintain integrity, accuracy and completeness of QC data and records.
• Meet quality objectives set by management & comply to Alcon, QMS and Safety requirements.
• Timely completion of all compliance activities without overdue, including but not limited to NCI, OOS, CAPA, Effectiveness Check, CR, training, periodic review.
• Timely report non-conformance or out-of-specification events. Lead or assist in root cause analyses for product defects and quality lapses, and take effective actions to prevent recurrence.
• Drive and promote the continuous improvement culture. Challenge current processes, identify improvements and drive the effort to implement lab system/process while maintaining compliance and reducing human Intervention.
• Review and assess external standard and/or regulatory requirements pertaining to quality control activities and implement necessary changes to ensure compliance
• Perform basic equipment troubleshooting.

WHAT YOU'LL BRING TO ALCON:

• Diploma (with at least 3 years) or Degree (with at least 1 year) in Chemistry, Biotechnology, or a related scientific discipline.
• Prior experience in a GMP-regulated laboratory environment is preferred.
• Familiarity with analytical techniques such as HPLC, UV-Vis etc.
• Strong attention to detail, documentation skills, and commitment to quality.
• Ability to work effectively in a team-oriented and fast-paced environment.
• Willingness to work rotational shift schedule across 3x shifts.

HOW YOU CAN THRIVE AT ALCON:

At Alcon, we are committed to fostering a work environment where our employees can grow, innovate, and excel. Here's how you can thrive in your role with us:

• Career Growth & Development – Gain access to continuous learning opportunities, leadership training, and career advancement programs to support your professional journey.
• Collaborative Culture – Work alongside passionate and diverse teams in a dynamic and inclusive environment that encourages innovation and teamwork.
• Impactful Work – Be part of a purpose-driven company that is improving lives by advancing eye care solutions worldwide.
• Recognition & Rewards – Your contributions are valued and recognized through competitive compensation, performance incentives and career progression opportunities.
• Global Exposure – Join a world-class organization with opportunities to collaborate across international teams and gain global industry insights.
• Work-Life Balance & Well-Being – Enjoy employee wellness programs, flexible work arrangements and initiatives that support your well-being.

At Alcon, we empower our people to make a difference while growing their careers in an exciting and supportive environment. Join us and see brilliance in every opportunity

ALCON Careers

See your impact at

ATTENTION: Current Alcon Employee/Contingent Worker

If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.

Find Jobs for Employees

Find Jobs for Contingent Worker

At Alcon, we are inspired by the meaningful work we do to help people see brilliantly. As the global leader in eye care, we boldly innovate, champion progress, and act with speed. We recognize and celebrate the contributions of our people, offering career opportunities that empower growth and fulfillment. Together, we go above and beyond to make a lasting impact on the lives of our patients and customers. We cultivate an inclusive culture and invite diverse, talented individuals to join us in shaping the future of eye care.

ROLE SUMMARY:

As a Technician II, Quality Control Lab – Chemistry, you will play a key role in supporting manufacturing operations by performing chemical analyses, maintaining laboratory equipment, and ensuring compliance with regulatory standards. This is an excellent opportunity for individuals passionate about laboratory work and quality assurance in a dynamic, regulated environment.

In this role, a typical day will include:

•    Perform testing and/or inspection on raw material, in-process material, finished products and monitoring activities.

•    Review/Approve testing documentation and test records. Maintain integrity, accuracy and completeness of QC data and records.

•    Meet quality objectives set by management & comply to Alcon, QMS and Safety requirements.

•    Timely completion of all compliance activities without overdue, including but not limited to NCI, OOS, CAPA, Effectiveness Check, CR, training, periodic review.

•    Timely report non-conformance or out-of-specification events. Lead or assist in root cause analyses for product defects and quality lapses, and take effective actions to prevent recurrence.

•    Drive and promote the continuous improvement culture. Challenge current processes, identify improvements and drive the effort to implement lab system/process while maintaining compliance and reducing human Intervention.

•    Review and assess external standard and/or regulatory requirements pertaining to quality control activities and implement necessary changes to ensure compliance

•    Perform basic equipment troubleshooting.

WHAT YOU'LL BRING TO ALCON:

•    Diploma (with at least 3 years) or Degree (with at least 1 year) in Chemistry, Biotechnology, or a related scientific discipline.

•    Prior experience in a GMP-regulated laboratory environment is preferred.

•    Familiarity with analytical techniques such as HPLC, UV-Vis etc.

•    Strong attention to detail, documentation skills, and commitment to quality.

•    Ability to work effectively in a team-oriented and fast-paced environment.

•    Willingness to work rotational shift schedule across shifts.

HOW YOU CAN THRIVE AT ALCON:

At Alcon, we are committed to fostering a work environment where our employees can grow, innovate, and excel. Here's how you can thrive in your role with us:

•   Career Growth & Development – Gain access to continuous learning opportunities, leadership training, and career advancement programs to support your professional journey.

•Collaborative Culture – Work alongside passionate and diverse teams in a dynamic and inclusive environment that encourages innovation and teamwork.

•    Impactful Work – Be part of a purpose-driven company that is improving lives by advancing eye care solutions worldwide.

•    Recognition & Rewards – Your contributions are valued and recognized through competitive compensation, performance incentives and career progression opportunities.

•    Global Exposure – Join a world-class organization with opportunities to collaborate across international teams and gain global industry insights.

• Work-Life Balance & Well-Being – Enjoy employee wellness programs, flexible work arrangements and initiatives that support your well-being.

At Alcon, we empower our people to make a difference while growing their careers in an exciting and supportive environment. Join us and see brilliance in every opportunity

At Alcon, we're passionate about enhancing sight and helping people see brilliantly. With more than 25,000 associates, we innovate fearlessly, champion progress, and act swiftly to impact global eye health. We foster an inclusive culture, recognizing your contributions and offering opportunities to grow your career like never before. Together, we make a difference in the lives of our patients and customers. Are you ready to join us?

This role is part of Alcon's Quality & Regulatory Affairs function, a team that ensures our products are in compliance with global, local, and internal regulations and meet the strictest standards of quality as we help people see brilliantly.Technician II, Quality Control Lab - Microbiology (Science/Tech/Engineering Path), is primarily responsible for handling complex microbiological tasks, analyzing samples, and developing methods to support product validation and compliance.

Specifics Include:

• Handle complex microbiological tasks, supporting operations and contributing to efficiency within defined procedures
• Analyze various microbiological samples, ensuring accuracy and precision of analyses
• Recommend corrective actions and develop methods to support product and process validation, product release, and compliance with regulatory and company standards
• Make minor decisions within the scope of tasks, requiring enhanced technical skills and problem-solving abilities
• Collaborate with affiliated departments to integrate lab results into the manufacturing process, driving problem-solving and innovation through scientific principles
• Adhere to GxP regulations by strictly following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation, ensuring rigorous quality control, and completing all required training
• Meet individual job requirements and contribute to the overall compliance of the organization by committing to continuous improvement and regulatory adherenceAll associates must adhere to GxP regulations by strictly following Standard Operating Procedures (SOPs), maintaining accurate and complete documentation, ensuring rigorous quality control, and completing all required training. Associates are responsible for meeting their individual job requirements and contributing to the overall compliance of the organization. Compliance with regulatory requirements and a commitment to continuous improvement are essential to our operations.

Qualifications: Associate shall have the appropriate education and experience to successfully perform the responsibilities/activities of this role.

ATTENTION: Current Alcon Employee/Contingent Worker

If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.

Find Jobs for Employees

Find Jobs for Contingent Worker

Responsibilities:

• Ensure adherence to the Change Control management systems and processes.
• Develop competency and proficiency in the QA Change Control process and the associated tools, supporting the delivery of training for change users as needed.
• Evaluate Change Control requests for process, validation, regulatory and product impact.
• Coordinate the review and approval process of change requests to ensure timely execution of changes.
• Ensure all site changes are managed appropriately to meet the expectation of the global change control board (if applicable) and meets site project timelines.
• Participate in cross functional and cross site change management forums.
• Collaborate with departments to ensure change control activities are executed efficiently and effectively, to provide supporting assistance to stakeholders in the process.
• Ensure completion of required change control actions prior to lifting lot disposition restrictions.
• Assist in the development and delivery of training materials and qualifications for Change Control processes and Change Management applications.
• Perform Change Records review in support of Annual Product Review activities.
• Ensure maintenance and continuous improvement of change control and processes.
• Support regulatory inspections and provide audit support with team, which may include presentations and facility, utility, equipment documentation review.
• Compliance with cGMP and site safety & security regulations at all times
• Any other duties as assigned by supervisor or manager.

About You:

• Bachelor's degree or higher in Biologics, Pharmacy, Pharmaceutical Engineering, Bioengineering, or other relevant fields.
• 3+ years of experience in a GMP-regulated biopharmaceutical or pharmaceutical
• manufacturing environment.

Job Type: Contract

Contract length: 12 months

Pay: $4, $8,000.00 per month

Experience:

• Change Control management systems: 3 years (Preferred)
• biopharmaceutical or pharmaceutical: 3 years (Preferred)
• qualifications for Change Control processes: 3 years (Preferred)

Working location: Tuas, Gul Circle

Working Hours : Mon - Fri 830am-6pm

Job Responsibilities:

1) Perform QC inspections for manufacturing department in-process parts

2) Have at least Zeiss CMM setting knowledge and programming knowledge

3) Provide support on new project CMM programming

4) Able to interact with other departments on observations and corrections

5) Ensure the fundamental quality plan is established, well understood and executed by all QC personnel

6) Monitor test production, and to perform quality planning, quality target and performance management

7) Recording inspection results by completing reports, summarizing re-works and wastes and inputting data into quality database

8) Investigate and assist production personnel, regarding product or process failure and determining their origin and cause, and to report recommendations to Superior

9) Training the production team on quality control measures to improve product excellence

10) Provide training and support to quality assurance team on systems, policies, procedures, and core processes

11) Able to read precision machining drawings and GD&T

12) Keeping measurement equipment operating accurately by following calibration requirements and calling for repairs

13) Actively support safety measurement in the workplace

14) Responsible for QC department document filing system

15) Had knowledge in milling or lathing is a plus

16) Other responsibilities may be assigned from time to time

Qualification :

At least 2 years of working experience in Precision Engineering field

Requirements :

1) Able to lead a group of QC to perform daily task and confirm to quality performance as per specification

2) Responsible for the on-site audit of customer and supplier, audit checklist and follow up the closure of non-conformance

3) Knowledge of ISO 9001:2015 Quality Management System

4)Able to communicate in Mandarin, in order to liaise with Mandarin speaking associate

Responsibilities:

• Support QA Manager to maintain Quality system
• Perform internal audit and ensure that quality system is in place at all times.
• Initiate root cause analysis and continuous improvement
• Maintain and conduct regular reviews of calibration and PM for instruments and equipment
• Responsible for the Corrective and Preventive Action relating to customer complaint
• Responsible for generating of Work Instruction which deem required for Guiding QA Op
• Ensure QA activities and operation is according to written procedures
• Generate monthly report/summary of OQA rejects, customer returns, RMA, external and interl 8D and revised specs and procedures
• Liaise with external auditors and certification bodies in conducting audits
• Perform any other duties, as assigned by superior

Requirements:

• Possess at least a Diploma in QA Engineering or equivalent.
• 1-2 years of relevant working experience in a manufacturing environment
• Able to operate or use basic measuring tools or equipments.
• Must have knowledge in QMS (ISO9001, ISO14001, IATF16949) and application in Quality Tools (FMEA, Control Plan, SPC, 8D problem-solving discipline structure
• Proficiency in Microsoft application (Excel, Word, and PowerPoint)
• Possess relevant knowledge of application of various QC analytical and troubleshooting tools.
• Able to work independently and willing to learn
• Self-driven and holds a positive learning attitude
• Good communication and interpersonal skills

Our client, a well-known Japanese company is looking for candidates for the position of Quality Assurance (QA) Engineer.

Responsibilities:

• Direct and Supervise WIP and Final Inspections
• Handle and Approve First Article Submission
• Understand and Ensure Compliance with customer's requirements
• Monitor, maintain and continually improve quality standards
• Resolve Quality issues with internal and external parties
• Supervise and maintain calibration of measuring equipment
• Review on non-conformances & approve disposition actions
• Create 8D reports
• Provide periodical quality review and trainings
• Involve in First Article Product and process development
• Assist in maintaining ISO Management System, reports, follow-up and closure
• Any other duties as assigned by the management.

Requirements:

• Diploma in Mechanical/ Manufacturing or related Engineering Field
• Minimum 3 years in related fields
• Knowledge on measuring and statistical techniques
• Must possess the knowledge on CMM (Coordinate Measuring Machine)
• Responsible, Positive Attitude and able to work well as a team
• Able to lead a team of quality operators

We regret that only shortlisted candidates will be notified.

PERSOLKELLY Singapore Pte Ltd | EA License No. 01C4394 | UEN No E

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