255 Lab Supervisor jobs in Singapore

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 Responsibilities

• Oversee and provide guidance to QC Inspection Team to ensure implementation of all inspection-related activities according to standards, including proper disposition and handling of non-conforming material/product.
  - Pre-inspection of designated goods (at warehouse).
  - Sampling and QC inspection of incoming materials (pre-shipment samples, raw materials, bulk, semi-finished and finished products, packaging materials) and out-going products.
  - In-process inspection to ensure that quality, hygiene, and safety standards are met.
• Identify and investigate OOS (out-of-specification) or NC (non-conformance) cases, analyse the root causes, and monitor closely the resolution and correction status.
• Investigate product feedbacks, analyse quality-related problems, and recommend problem resolution.
• Perform testing on samples of new raw materials, products, packaging etc., or arrange for lab testing (including stability study as required).
• Perform QC inspection and product-related performance data measurement and analysis.
• Work with relevant parties to establish specifications and quality attributes of raw material, packaging and product, confirm appropriate test method for each QC parameter, and document evidence.
• Contribute for establishing and improving relevant QC SOP and inspection/testing-related work instructions (in compliance with GMP and ISO requirements).
• Ensure proper QC documentation including Master Specifications, QC Records (including electronic logs), QC Test Reports, Lab Test Reports, Non-Conformance Reports, COA etc.
• Establish and maintain product stability testing guideline.
• Support and assist Quality Assurance on External Provider Quality Management.
• Ensure cleaning and environmental monitoring programmes for the site are done accordingly.
• Manage retention room for retention, reference and post-inspection samples, and sample retention system.

Requirements

• Degree in Science or Engineering (preferably in Cosmetic Science, Chemistry, Pharmacy, Nutrition or relevant field)
• Preferably 2 years of working experience in the quality control of cosmetics, pharmaceuticals, dietary supplement, food, or skincare/medical device. Fresh Graduates are welcome to apply too.
• Experience in a GMP environment or with knowledge of GMP.
• Knowledge of relevant product standards, quality control and test methods.
• Stringent compliance to procedures, guidelines, standards, and regulations.
• Self-starter, good at working well independently with initiatives.
• Meticulous & detail oriented.
• Analytical & problem-solving skills.
• Time management skills (scheduling, prioritising) to meet deadlines.

Job Responsibilities

• Read specifications and inspection & test plans to understand the requirements of products.

• Perform scheduled sampling quality inspections of incoming materials/ products from external provider and outgoing products for shipping.

• Conduct scheduled in-process inspection in the production line to ensure that quality, hygiene and safety standards are met.

• Reject and report to QCI Supervisor/ Manager for all products and materials that fail to meet quality specification and expectations.

• Ensure QC inspection record/ log is updated for inspection and testing conducted.

• Assist QC Specialist for any investigation for product-related non-conformance issue and recommend problem resolution.

• Assist QC Specialist for establishment of QC inspection test methods.

• Manage retention room for reference and post inspection samples.

• Maintain External Laboratory Service Providers register, perform external laboratory product testing and test report record retention.

• Perform routine QC laboratory 5S maintenance tasks.

• Perform other duties as assigned.

Requirements

• Higher Nitec or equivalent qualification.

• Experience in QC inspection and strong understanding of relevant QC standards and testing techniques.

• Certification in quality control is preferred.

• Understand basic laboratory equipment handling.

• Working well independently and detail-oriented.

Other Information

• Basic + 13th month + Variable Bonus

• Medical benefits, insurance and free company products

Job Responsibilities

• Read specifications and inspection & test plans to understand the requirements of products.

• Perform scheduled sampling quality inspections of incoming materials/ products from external provider and outgoing products for shipping.

• Conduct scheduled in-process inspection in the production line to ensure that quality, hygiene and safety standards are met.

• Reject and report to QCI Supervisor/ Manager for all products and materials that fail to meet quality specification and expectations.

• Ensure QC inspection record/ log is updated for inspection and testing conducted.

• Assist QC Specialist for any investigation for product-related non-conformance issue and recommend problem resolution.

• Assist QC Specialist for establishment of QC inspection test methods.

• Manage retention room for reference and post inspection samples.

• Maintain External Laboratory Service Providers register, perform external laboratory product testing and test report record retention.

• Perform routine QC laboratory 5S maintenance tasks.

• Perform other duties as assigned.

Requirements

• Higher Nitec or equivalent qualification.

• Experience in QC inspection and strong understanding of relevant QC standards and testing techniques.

• Certification in quality control is preferred.

• Understand basic laboratory equipment handling.

• Working well independently and detail-oriented.

Other Information

• Basic + 13th month + Variable Bonus

• Medical benefits, insurance and free company products

Company: COWAY ENGINEERING & MARKETING PTE LTD – Seletar

COWAY ENGINEERING & MARKETING PTE LTD is hiring a Full-time Quality Control Inspector in Seletar, Singapore. Apply now to join our team.

Job summary:

• Flexible working hours available
• 2-3 years of relevant work experience required
• Expected salary: $1,600 - $3,000 per month

Main Duties and Responsibilities:

1. Perform receiving, in-process, and final inspection on aircraft components.
2. Raise shop-floor findings if discrepancies are found.
3. Ensure all measuring equipment used for inspections is properly maintained and calibrated.
4. Assist in managing parts in and out of quarantine store.
5. Review maintenance documents for compliance before they are kept as quality records.
6. Maintain cleanliness of the work area.
7. Provide support for secondary tasks as assigned by superiors or management.

Requirements:

• Qualification: At least Secondary 4 or equivalent
• Experience in QC, hardworking, willing to learn
• Ability to interpret engineering drawings
• Ability to operate measuring equipment
• Knowledge of CMM machines is an advantage
• Proficiency in Microsoft Office, especially Excel
• Ability to work in a fast-paced environment

Note: Be cautious when applying. Do not share bank or credit card details, and report suspicious job ads.

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.

Key Responsibilities

• Manage the storage and inventory of laboratory samples
• Conduct analytical testing and documentation for APIs, drug substances/products, complaints, packaging materials, and stability samples
• Ensure strict compliance with cGxP standards, including data integrity requirements
• Execute and document stability testing (if not centralized), including storage, testing, and reporting to cGxP standards
• Follow all Health, Safety, and Environment (HSE) guidelines
• Identify and report safety risks or potential incidents, and propose preventive solutions
• Participate in mandatory training and retraining programs
• Support operations during rotating day/night shifts

Role Requirements

Essential Qualifications and Experience

• Prior experience in a laboratory setting within the pharmaceutical industry (QA, production), with exposure to aseptic techniques preferred
• Proficiency in administrative and documentation tasks compliant with GMP and HSE standards
• Demonstrated strengths in:
• Breakthrough analysis and problem-solving
• Resilience and adaptability
• Operational efficiency and continuous learning
• Digital fluency and technical skills

Technical Competencies

• Hands-on knowledge of laboratory instruments and QC testing procedures
• Strong command of GxP, TQM principles, and lab excellence standards
• Ability to maintain QC IPC/DS laboratory equipment and systems in accordance with cGMP compliance
• Competent in executing product testing within timelines and contributing to validation and method transfer protocols
• Skilled in performing routine in-process, release, and stability testing, including documentation review
• Capable of supporting lab investigations and leading root cause analysis
• Detail-oriented in preparing and verifying QC documentation to ensure accuracy, consistency, and regulatory compliance
• Proactively identifies opportunities to optimize testing procedures
• Supports audit readiness and participates in internal audits and inspections by health authorities

Responsibilities:

• Online Quality Checking (Metal Detector, Cooker, Pasteurizer, Steamer)
• Online Finished Product Testing
• Monthly Verification of CCP (Critical Control Point)
• Online Verification Sampling for Microbial Analysis
• Internal Calibration of Weighing Scales
• Verification on goods return
• Handle Customers’ Complaint
• Conduct routine physical, chemical, sensory and other analyses accordingly.
• Take appropriate decisions for rework of material based on historical trend and in consultation with seniors
• Raise non-conformation for quality deviations of Raw Material/Finished Goods and follow up with proper closure of corrective and preventive action
• Initiate actions to investigate customer complaint in consultation with relevant team members
• Collect comprehensive evidence/crucial data, provide sound reasoning and propose possible root cause for customer complaints and internal rejection
• Maintain up-to-date quality control programs, policies, process workflows, procedures and work instructions

REQUIREMENTS:

• Diploma / Degree in Food Science preferred
• At least 2 years of relevant experience will be considered for Senior position
• Experienced and passionate in Continuous Improvement
• Exceptional problem-solving skills
• Good Knowledge of Quality Management Systems (HACCP, BRC, ISO 22000)
• Good Communication, Organizational and Analytical Skills
• Strong ability to work well in a team and independently
• Excellent IT skills, particularly in MS Excel, PowerPoint, Word, Access
• Ability to work with multiple priorities in a fast-paced environment is required.
• 5 Days Work Week + 1 Saturday
• Undertake any other ad-hoc projects/ tasks assigned
• Job Scope, Work Day and Work Hours subject to changes depending on work requirement
• Fresh grads are welcome
• Salary package commensurate with experience

Job Responsibilities

• Read specifications and inspection & test plans to understand the requirements of products.
• Perform scheduled sampling quality inspections of incoming materials/ products from external provider and outgoing products for shipping.
• Conduct scheduled in-process inspection in the production line to ensure that quality, hygiene and safety standards are met.
• Reject and report to QCI Supervisor/ Manager for all products and materials that fail to meet quality specification and expectations.
• Ensure QC inspection record/ log is updated for inspection and testing conducted.
• Assist QC Specialist for any investigation for product-related non-conformance issue and recommend problem resolution.
• Assist QC Specialist for establishment of QC inspection test methods.
• Manage retention room for reference and post inspection samples.
• Maintain External Laboratory Service Providers register, perform external laboratory product testing and test report record retention.
• Perform routine QC laboratory 5S maintenance tasks.
• Perform other duties as assigned.

Requirements

• Higher Nitec or equivalent qualification.
• Experience in QC inspection and strong understanding of relevant QC standards and testing techniques.
• Certification in quality control is preferred.
• Understand basic laboratory equipment handling.
• Working well independently and detail-oriented.

Other Information

• Basic + 13th month + Variable Bonus
• Medical benefits, insurance and free company products