235 Food Processing Industries jobs in Singapore

As a Quality Control Specialist, you will play a vital role in ensuring the quality of our products.

Your responsibilities will include performing inspections and verifications of incoming materials, in-process production, and finished goods to meet customer requirements.

You will also be responsible for maintaining and calibrating measuring equipment, documenting inspection results, summarizing rework and waste, and inputting data into our quality database.

In addition, you will be responsible for cleaning and packaging finished goods according to specified requirements and standards, helping with sorting, labeling, and moving materials as required, meeting production deadlines, and ensuring all packaging is done accurately and in line with quality standards.

You will report any issues or discrepancies in the production or packaging process to your manager and perform any other related duties assigned by your immediate superior.

To succeed in this role, you must adhere to all workplace safety rules and guidelines.

The ideal candidate will have a Certificate/ITE/NITEC/ Higher NITEC in Precision Engineering/Mechanical or equivalent, and be able to read and interpret drawings with a good understanding of geometric dimension and tolerance.

You will also need to be familiar with caliper, micrometer, gauges, tape measure, CMM, and team players with dependable attitudes are preferred.

This role is responsible for ensuring that products meet established standards through rigorous audit checks.

• Audit in-coming and outgoing products according to established policies.
• Perform all product processes within the section, including reworks, repairs, and defective photo-taking.

Maintain accuracy and completeness of supplier invoice data and quality control data in our system. Develop standard operating procedures for handling storage and stock inventory.

This position plays a critical role in achieving Company quality targets.

Our Client is a Singapore based company in Medical Devices. Due to business needs, they are now recruiting a QC Supervisor to be part of their Quality team for ongoing transformation projects. They are located at West.

Duties:

• Guide and coach lab technicians.
• Inspect raw materials and conduct analyses on WIP and finished product samples.
• Support QA in failure analysis, corrective actions, and customer complaints.
• Assist with GMP audits, validations, and maintaining quality and technical files.
• Prepare technical reports, standards, and specifications for processes and products.

Requirements

• Minimum Diploma in Chemical/ Biotechnology or related field
• Possess supervisory experience in leading a team of technicians

Interested candidates who wish to apply for the advertised position, please click APPLY NOW or email an updated copy of your resume/cv.

We regret that only shortlisted candidate will be notified.

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About the Role

We are seeking a QC Analyst to support quality control operations within our biotech drug substance site. The role is responsible for executing laboratory testing, sample management, and equipment maintenance in compliance with cGxP standards, ensuring the quality and timely delivery of products.

Key Responsibilities

• Perform analytical testing and documentation of raw materials, drug substances, drug products, packaging, complaints, and stability samples
• Manage sample storage and stability programs
• Maintain, calibrate, and qualify laboratory equipment
• Ensure compliance with cGxP, data integrity, and HSE guidelines
• Participate in training and contribute to continuous improvement initiatives

Performance Measures

• Accurate and timely completion of analysis and documentation
• Compliance with GMP, SOPs, and regulatory standards
• Readiness for inspections with no critical findings
• Contribution to cost and process optimization

Qualifications & Experience

• Diploma, apprenticeship, or equivalent training in a relevant scientific field (e.g., Chemistry, Biochemistry, Biotechnology, Life Sciences)
• Preferably with 2-5 years of experience in a pharmaceutical laboratory environment (QC, QA, or production)
• Knowledge of GMP/cGxP standards, laboratory techniques, and QC processes
• Strong teamwork, resilience, and problem-solving skills
• Basic proficiency in English

Why Join Us

This role offers the opportunity to directly impact product quality, compliance, and patient safety while working in a collaborative and innovative environment.

Your Role

• Perform checks on the structural, architectural and M&E materials/works to ensure that the final touch-up works are ready for inspections
• Monitor the performance of subcontractor workers for all trades and ensure any defects are properly rectified
• To participate, work closely and give support to safety personnel at site on all initiatives/ matters relating to Safety and Health
• To comply with the Company Safety Management System and the WSHA and its subsidiary legislation

The Requirements

• Possess a Degree in Civil Engineering or its equivalent
• Minimum 3-5 years of relevant working experience in construction industry
• Must be technically inclined and possesses excellent problem-solving
• Be able to work independently as well as acquiring good interpersonal skills to coordinate between the various disciplines and construction teams

Product and Raw Materials Testing:

• Develop and qualify method of analysis (MOA) for QC lot release testing
• Perform analytical testing such as flow cytometry (FACS) and qPCR assay to support QC lot release.
• Perform stability testing of released final products as per protocol and timeline.
• Perform functional/comparability testing of raw materials such as plasmid, media, reagents and etc.
• Support assessment of certification/accreditation and services provided by external labs for QC lot release testing

Documents and Data Management

• Drafting and updating of relevant SOPs and specification documents for lab, equipment, test method, training and raw materials.
• Author and review technical protocols and test reports, develop guidelines and standard practices for data documentation and analysis.
• Review test results, document data and produce trends in an efficient, organised and presentable manner to facilitate discussions, and to support business and performance metrics reporting.

Deviations and Audit Management

• Assist OOS/test deviations initiation, investigations, root cause analysis and CAPA implementation for product defects and quality lapses.
• Support internal and external audits/inspections.

Equipment and Lab Management

• Monitor and schedule equipment calibration and maintenance as per schedule and site master file.
• Perform lab housekeeping, equipment, inventory, lab cleaning and biohazard/waste management.
• Perform monitoring and procurement of lab inventory, for e.g. materials and cosumables.

Continuous Improvement

• Implement initiatives to encourage improvement of QC procedures, activities and workflows.
• Conduct routine literature review through established publication channels to ensure continual knowledge proficiency on both GMP and current technological trends relevant to CellVec activities.

About the Role:

We are looking for a QC Analyst (Microbiology) to support our QC lab operations, ensuring testing and documentation are completed accurately and in compliance with cGMP standards.

Responsibilities:

• Perform routine microbiological testing of raw materials, drug substances, finished products, and packaging/stability samples.
• Manage sample handling, storage, and documentation.
• Ensure compliance with cGxP, GMP, HSE, and data integrity requirements.
• Support audits, inspections, and laboratory equipment documentation.

Requirements:

• Diploma/Degree in Microbiology, Biotechnology, Life Sciences, or related field.
• Preferably with lab or pharmaceutical industry experience.
• Knowledge of aseptic techniques, microbiological methods, and GxP standards an advantage.
• Strong attention to detail, teamwork, and communication skills.

Why Join Us?

• Be part of a global biotech/pharma company committed to quality and patient safety.
• Gain hands-on laboratory experience in a regulated environment.
• Continuous learning and professional growth opportunities.
• Collaborative and supportive work culture.

Quality Control Technician page is loaded# Quality Control Technicianlocations:
Singapore, SGPtime type:
Full timeposted on:
Posted Todayjob requisition id:
R Air Liquide Advanced Materials is actively seeking a Quality Control Technician to be located at our Singapore manufacturing facility. Reporting to the Quality Manager, the Quality Control Technician will represent Quality on the manufacturing teams by supporting analysis, managing the analyzers, and supporting investigations. Independent judgment is required to plan, prioritize, and organize diversified workload and recommend changes to continuously improve practices and procedures.* Work within a highly structured environment that emphasizes safety and strict adherence to established operating procedures, including ISO directives and a formalized PPE program. Drive a culture of "Do It Safe, Do It Right the First Time" by observing and reporting hazards, and assisting in the investigation of production defects and supporting the Quality Team in control of non-conforming materials.* Analyze various materials using multiple analytical techniques like GC, FTIR, and process analyzers. Accurately document and input analytical data into all necessary databases and provide guidance to disposition lots.* Maintain and assist with the repair of analytical instrumentation, including performing preventive maintenance and adhering to all necessary calibration requirements within lab operations.* Participate in continuous improvement initiatives for analytical process systems.* Prioritize daily tasks and coordinate with the production and quality teams. Work cooperatively with production staff to meet operational goals.* Adhering to Training and Policies and to complete all assigned training.# ___________________# * Diploma or Nitec in Chemical Process Technology (or an equivalent qualification)* At least two years of experience in a process operations environment.* Possesses 1 year of analytical experience, specifically with Gas Chromatography (GC) and Fourier-Transform Infrared Spectroscopy (FTIR).* Possesses a solid understanding of quality systems and strong troubleshooting skills.* Proficient in Microsoft Excel and other software systems like LIMS, SAP, and Google. The ability to learn new systems quickly is essential.* Able to work rotating shifts.**We thank you for your interest in Air Liquide. Interested applicants are encouraged to send in a detailed resume, including reasons for leaving for past employment. Please be informed that only shortlisted candidates would be notified.****Our Differences make our Performance**At Air Liquide, we are committed to build a diverse and inclusive workplace that embraces the diversity of our employees, our customers, patients, community stakeholders and cultures across the world.
We welcome and consider applications from all qualified applicants, regardless of their background. We strongly believe a diverse organization opens up opportunities for people to express their talent, both individually and collectively and it helps foster our ability to innovate by living our fundamentals, acting for our success and creating an engaging environment in a changing world.locations:
Singapore, SGPtime type:
Full timeposted on:
Posted 30+ Days AgoA world leader in gases, technologies and services for Industry and Health.
Through the passion and diversity of its people, Air Liquide leverages energy and environment transition, changes in healthcare and digitization, and delivers greater value to all its stakeholders.
Join us for a stimulating experience: you’ll find a world of learning and development opportunities where inventiveness is at the heart of what we do, in an open, collaborative and respectful environment.***Discover what your professional journey at Air Liquide could be** **!***We want to ensure a safe experience for everyone interested in joining Air Liquide. Please be aware of fraudulent job offers that are circulating, falsely using the Air Liquide name and brand. These scams often involve individuals or organizations impersonating Air Liquide recruiters or employees through fake emails, social media, and websites. They may attempt to request personal information or, critically, ask for payment for various reasons like application fees, training, or visa processing. **Please be advised that Air Liquide and our authorized recruitment partners will never ask you for money at any stage of the recruitment process.**You may verify job postings through our official global
at any time. If you receive a suspicious job offer or request for payment/sensitive data, we strongly advise that you do not respond or click on any links. We encourage you to verify the source carefully and only interact through our official channels. We appreciate your interest in Air Liquide and are committed to combating these fraudulent activities to protect job seekers. If you wish to report an incident, please contact us via this
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Develop, implement, and oversee project-specific QA/QC plans, inspection protocols, and checklists.
Ensure construction works meet BCA CONQUAS and Quality Mark standards.
Lead quality inspections, audits, and evaluations across all trade disciplines.
Collaborate with consultants, subcontractors, and internal teams to address and resolve quality-related issues.
Monitor on-site activities to ensure compliance with project specifications and quality requirements.
Review and approve materials and method statements in line with project standards.
Maintain accurate records of inspections, non-conformance reports, and corrective actions taken.
Train and support site teams in adhering to quality standards and implementing best practices.
Prepare the site for CONQUAS and Quality Mark assessments, including mock-up inspections and scoring strategies.
Drive continuous improvement initiatives to enhance overall quality performance.
Oversee material testing, as well as mock-up, PMU, and VMU processes for façade works.
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