382 Dairy Production jobs in Singapore

• 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)

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 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

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

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 .

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Join to apply for the Quality Control Specialist role at Cytiva

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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

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Job Information

· Salary Package: Basic (starting from 2k) + Performance Bonus

· Other Benefits: Medical & Dental coverage

· Working Days: Monday – Friday + Half-day Saturday

· Working Hours: 8.30am – 5.30pm (Weekdays), 8.30pm – 12.30pm (Saturday)

· Working Location: Ubi/Eunos

· Job Contract: Full-time Permanent role

• Perform daily, weekly & monthly inspection reports.
• Analyse and trouble-shooting production quality issues.
• Material receiving inspection
• Disposition of non-conforming products (incoming & outgoing).
• Handle customers’ complaint (CAR) with effective corrective actions.
• Provide training to QC inspectors.
• Liaise with client inspector on inspection point(s).
• Conduct regular line audit and drive for quality improvement.
• Conduct internal ISO audit and manage external customer audit.
• Conduct PMI, Pressure & PT tests
• To keep and update all the Welding Procedure Specifications (WPS) and
  Procedure Qualification Records (PQR)
• To keep and update all non-conformance reports (NCR), follow-up sheet, calibration status report of measuring and test equipment.
• Carry out any other duties as and when assigned by the immediate supervisor or higher management.

Requirements

• 2 years relevant working experience in related industries
• ASNT Level II
• Attention to Detail
• Strong written and verbal communication skills
• Effective time management
• Independent & keen learner
• Flexible and adaptable
• Able to manage high levels of stress
• Proficient in Microsoft applications: Outlook, Excel, Word, Power Point, etc.

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