257 Quality Control jobs in Singapore

Quality Control Supervisor / Manager | 5 Days | Up to $4.5k | Redhill - 4769

Singapore, Singapore THE SUPREME HR ADVISORY PTE. LTD.

Posted 4 days ago

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full time
Quality Control Supervisor / Manager | 5 Days | Up to $4.5k | Redhill

Location: Jalan Kilang ( Nearest mrt Redhill )
Working days: 5 days ( Mon - Fri )
Working hours: 8:30am - 6pm
Salary : $,500 - 4,500

Job Duties and Responsibilities:

Quality Functions:
  • Responsible for the operations of the Quality Control Lab.
  • Ensure that all lab analyses (starting materials, packaging materials, intermediates and finished products, stability samples etc.) are done in a timely manner, according to established test method and to provide accurate results.
  • Prepare or revise Standard Operating Procedures (SOPs) relevant to product quality.
  • Prepare or revise Specifications, Test Methods and Quality Control Procedures for all starting materials, intermediates and finished products.
  • Ensure the maintenance of reference and retention samples
  • Ensure that on-going stability studies are conducted for finished products as per cGMP requirements
  • Perform sampling and testing of Starting Materials (Packaging) in accordance with Standard Operating Procedures (SOPs) in a timely manner.
  • Perform Product testing in accordance with Standard Operating Procedures (SOPs) in a timely manner.
  • Perform Analytical Method Validation and Cleaning Method Validation
  • Assist in validation or revalidation of manufacturing processes
  • Handle installation, operation, calibration and maintenance of lab instruments.
  • Maintain good lab practice, lab safety, inventories and housekeeping programs.
  • Participate in the investigation of product complaint in evaluation of returned goods relating to product quality.
  • Perform supplier qualification.
  • Conduct and coordinate Out-Of-Specification/Deviations/atypical results investigation.
  • Review Changes, Deviations, Corrective and /or Preventive Actions as Area/Process Owner.
  • Ensure that the required initial and continued training is carried out to quality control personnel.
  • Maintain all Quality Control documents and records.

Requirements:
  • Candidate must possess a Degree in a relevant Science field or related discipline
  • Lab experience in a Chemistry related field
  • Hands-on experience in GC
  • Must have experience in Analytical Method Validation
  • Knowledge of GLP


The Supreme HR Advisory Pte Ltd | 14C7279

Ong Boon Kiet (Travys) | R22104769

Senior Recruitment Consultant
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Quality Control Executive (FRESH GRADS WELCOMED)

Singapore, Singapore MOLEAC PTE. LTD.

Posted 4 days ago

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Job Descriptions

full time
Department: CMC

Location: Singapore

ESSENTIAL DUTIES & RESPONSIBILITIES

Quality Control

• Conduct incoming material QC check as per Acceptable Quality Limits (AQL) plan and Standard Operating Procedure (SOP)

• Assist to track and update external QC lab testing status and report documentation for raw materials, excipients and finished products in Production-QC tracker

• Conduct batch release documentation according to established specifications and requirements of raw materials and finished product to ensure commercial order fulfilment

• Assist to track and update Stability Studies reports status to provide support to product Stability Studies program.

• Provide support in QC testing invoice verification prior to submission for finance processing.

• Provide support in QC systems improvement and development according to cGMP and Pharmacopeia standards.

• Ensure smooth product release to support production planning.

Production support

• Work closely with supply chain on in/out flowing goods and ensure proper inventory levels of materials

• Coordinating and arranging of production / packing jobs with contract manufacturers and updating of its progress in the production tracker

• Liaising with Contract Manufacturers, vendors and suppliers to prepare delivery notes and/or collection notes to facilitate stock movement

• Provide support in verification of invoices from suppliers and service providers prior to submission for finance processing.

• Ensure Good Distribution Practices (GDP) compliance and provide support to the department on system improvements and work processes.

Qualifications:

• Higher Nitec / Diploma in pharmaceutical sciences, chemical engineering, or other chemistry-related disciplines.

• Good written and verbal communication skills. (This role requires liaising with suppliers/manufacturers in China).

• Good time and task management and coordination skills

• Good attention-to-detail skills
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QUALITY CONTROL MANAGER

Singapore, Singapore LI LI SHUN WOODWORK PTE. LTD.

Posted 4 days ago

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Job Descriptions

full time
Job Description

Job Scope & Responbilities :

* Handle for full set of account

* Financial month end closing

* Coordinate and liaise with external parties like auditors, tax agents and tax authorities

* Responsible for all duties related to Human Resources,

* Monthly payroll preparation, CPF submission

* Responsible of IRAS AIS,IR8A, Corporate tax, Income tax etc.

* MOM WPOL/EPOL/ matter

* Handling other admin duties

* Perform any other ad hoc duties when required.

Job Requirements :

* Candidate must possess at least diploma or equivalent.

* Language: Bilingual in English and Chinese Mandarin (read, write and speak) as the incumbent needs to liaise with Mandarin-speaking associates in the course of work.

* At least 2 Year(s) of working experience in the related field is required for this position.
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Quality Control Manager

Singapore, Singapore FONDA GLOBAL ENGINEERING PTE. LTD.

Posted 4 days ago

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Job Descriptions

full time
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
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Associate Manager, Quality Control

Singapore, Singapore WEST PHARMACEUTICAL SERVICES SINGAPORE PTE. LTD.

Posted 4 days ago

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Job Descriptions

full time
Job Summary:

In this role, you will
  • Be accountable for day-to-day performance of team/s safety, quality, delivery, cost and productivity
  • Manage teams of QC Technicians & Team Leads in execution of QC processes, schedule and personnel to ensure smooth operational activities work-flow and work compliance
  • Promote better quality mindset through inter-department collaborations

Essential Duties and Responsibilities:
  • Oversee resource management and team schedules for smooth execution of daily operational tasks in QC while meeting daily inspection targets and support Work In Progress (WIP) controls within team/s
  • Ensure proper product release and rework activities per procedures to support delivery requirements
  • Lead product characteristics trend monitoring with effective escalation and follow-ups
  • Demonstrate leadership, teamwork, and problem-solving support to resolve escalated operational issues collaboratively and ensure proper batch segregation
  • Define goals, clearly communicate these objectives and monitor/correct/recognize work performance respectively. Coach and counsel QC employees
  • Manage and resolve QC employee's relation issues and disputes
  • Manage onboarding activities for new QC employees for training and qualification
  • Manage ongoing activities for existing QC employees for training and requalification
  • Identify future training needs and enhance QC employees career opportunities
  • Responsible to review SOI revisions to enhance improvements for better workflow
  • Manage Deviation/Out-of-Spec report closures, batch dispositions while ensuring proper root cause analysis and CAPA identification
  • Accountable for on time operational updates for Tier 1, Tier 2, Tier 2.5 & Tier 3 of the LDMS system
  • Attend Tier 2, Tier 2.5 as QC representative, and facilitate Tier 1 (Shift Start Up) within QC
  • Promote and support site initiatives including safety programs, lean initiatives, training programs and consistently interpret and apply policies, procedures among employees
  • Manage non-routine requests from departments (eg validations, investigations, improvements, projects, product transfers, non-routine testings, non-conformance reports, etc)
  • Other duties as assigned by superior

Basic Qualifications:
  • Academic qualification of bachelor's degree in engineering or relevant fields
  • Computer literate and good grasp of Microsoft Office
  • Preferably 8 years work experience in QA/QC related activities
  • Added advantage with SAP, cGMP, Basic Lean and/or ISO working experience
  • Preferably with exposure to medical device, pharmaceutical or related manufacturing environment
  • Preferably minimum 5 years work experience managing a QC team
  • Able to work independently with minimum supervision

Preferred Knowledge, Skills and Abilities:
  • Able to be aware of all relevant standard operating procedures as per Company policy
  • Support and contribute to Lean Sigma programs and activities towards delivery of the set target
    Minimize waste, always ensure efficient work execution by continuous improvements
  • Able to comply with the company's safety policy at all times
    Ensure use of Personal Protective Equipment (PPE) in respective work environments for all members within the shift/s
    Report unsafe conditions or acts to responsible persons for corrections and improvements
    Ensure risk assessment control practices are adopted per HIRA for all members within the shift/s
    Ensure all legal licenses required for the proper usage of QC equipment are effective for all members within the shift/s
  • Able to comply with the company's quality policy at all times
    Lead monitoring / improvement activities to enhance operational support activities
    Participate in establishment and maintenance of documented procedure
  • Excellent communication & teamwork skills
  • Self-motivated and positive thinking
  • Ability to remain calm and professional under pressure
  • Proficiency in workplace English for work applications and interfaces
  • Time management skills

Physical and Mental Requirements:
  • Manufacturing environment with rotating working shift patterns
  • Overtime and being on-call are required. Occasionally required to work on different shift patterns
  • 20/30 Vision minimum, at near and/or far with at least one eye with or without corrective lenses and no color deficiency
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Quality Control (QC) Technician

Singapore, Singapore PANASONIC INDUSTRIAL DEVICES SINGAPORE PTE. LTD.

Posted 4 days ago

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Job Descriptions

full time
Job Summary

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.

Key Responsibilities

  • 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.

Required Qualifications

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

Preferred Skills & Experience

  • 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.

Preferred Qualities

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

Why Work With Us?

  • 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)

About Us

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.
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Quality Control Lead [Chemistry Lab | GC / GLP] - SM09

Singapore, Singapore THE SUPREME HR ADVISORY PTE. LTD.

Posted 4 days ago

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Job Descriptions

full time
Quality Control Supervisor / Manager

Location: Jalan Kilang ( Nearest mrt Redhill )
Working days: 5 days ( Mon - Fri )
Working hours: 8:30am - 6pm
Salary : $3,500 - $4,500

Job Duties and Responsibilities:

Quality Functions:
  • Responsible for the operations of the Quality Control Lab.
  • Ensure that all lab analyses (starting materials, packaging materials, intermediates and finished products, stability samples etc.) are done in a timely manner, according to established test method and to provide accurate results.
  • Prepare or revise Standard Operating Procedures (SOPs) relevant to product quality.
  • Prepare or revise Specifications, Test Methods and Quality Control Procedures for all starting materials, intermediates and finished products.
  • Ensure the maintenance of reference and retention samples
  • Ensure that on-going stability studies are conducted for finished products as per cGMP requirements
  • Perform sampling and testing of Starting Materials (Packaging) in accordance with Standard Operating Procedures (SOPs) in a timely manner.
  • Perform Product testing in accordance with Standard Operating Procedures (SOPs) in a timely manner.
  • Perform Analytical Method Validation and Cleaning Method Validation
  • Assist in validation or revalidation of manufacturing processes
  • Handle installation, operation, calibration and maintenance of lab instruments.
  • Maintain good lab practice, lab safety, inventories and housekeeping programs.
  • Participate in the investigation of product complaint in evaluation of returned goods relating to product quality.
  • Perform supplier qualification.
  • Conduct and coordinate Out-Of-Specification/Deviations/atypical results investigation.
  • Review Changes, Deviations, Corrective and /or Preventive Actions as Area/Process Owner.
  • Ensure that the required initial and continued training is carried out to quality control personnel.
  • Maintain all Quality Control documents and records.

Requirements:
  • Candidate must possess a Degree in a relevant Science field or related discipline
  • Lab experience in a Chemistry related field
  • Hands-on experience in GC
  • Must have experience in Analytical Method Validation
  • Knowledge of GLP

WhatsApp: (Shermaine)

Siah Sze Ming Reg No: R24125414

The Supreme HR Advisory Pte Ltd EA No: 14C7279
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Quality Control Technician

Singapore, Singapore JULIAN GREY CORPORATE ADVISORY PTE. LTD.

Posted 4 days ago

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Job Descriptions

full time
Company's Profile
Julian Grey's client offers customized solutions to meet evolving societal demands in the world of sustainability.

Responsibilities
  • Report to Section Engineer or designee and assist in QA Section tasks as needed
  • Perform lab tests, maintain equipment, and ensure facility cleanliness and upkeep
  • Prepare standards, reagents, and manage ISO documentation and raw data for QA
  • Conduct maintenance, troubleshooting, and document actions
  • Update and monitor SPC charts, ensuring accuracy
  • Assist in QC staff training and support audit preparation
  • Manage storage sample inventory, verify and receive QA purchases
  • Identify near misses, recommend improvements, and follow EHS/QMS procedures and 5S standards

Requirements
  • Experience with analytical instruments (e.g., ICP-MS, AAS)
  • Basic knowledge of ISO 9001, ISO 14001, and OHSAS 18001 standards is a plus

Benefits
  • Transportation allowance provided

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Please WA Justine @ 9755 9161
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Justine Lam Nyok Yuen
Reg No. R1218722
Julian Grey Corporate Advisory Pte. Ltd.
EA License No: 19C9568
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Quality Control Technician

Singapore, Singapore JULIAN GREY CORPORATE ADVISORY PTE. LTD.

Posted 2 days ago

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Job Descriptions

full time
Company's Profile
Julian Grey's client offers customized solutions to meet evolving societal demands in the world of sustainability.

Responsibilities
  • Report to Section Engineer or designee and assist in QA Section tasks as needed
  • Perform lab tests, maintain equipment, and ensure facility cleanliness and upkeep
  • Prepare standards, reagents, and manage ISO documentation and raw data for QA
  • Conduct maintenance, troubleshooting, and document actions
  • Update and monitor SPC charts, ensuring accuracy
  • Assist in QC staff training and support audit preparation
  • Manage storage sample inventory, verify and receive QA purchases
  • Identify near misses, recommend improvements, and follow EHS/QMS procedures and 5S standards

Requirements
  • Experience with analytical instruments (e.g., ICP-MS, AAS)
  • Basic knowledge of ISO 9001, ISO 14001, and OHSAS 18001 standards is a plus

Benefits
  • Transportation allowance provided

Follow us for more updates, interview tips!



Our telegram channel for job opportunities -

Interested Applicants
Please WA Justine @ 9755 9161
Shortlisted candidates will be notified

Justine Lam Nyok Yuen
Reg No. R1218722
Julian Grey Corporate Advisory Pte. Ltd.
EA License No: 19C9568
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Quality Control Specialist

Singapore, Singapore GLOBAL LIFE SCIENCES SOLUTIONS SINGAPORE PTE. LTD.

Posted today

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Job Descriptions

full time
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

Who you are:
  • 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

It would be a plus if you also possess previous experience in:
  • 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.
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