314 Water Quality jobs in Singapore

As an Infoscion at Infosys, your primary responsibility will involve ensuring effective Design, Development, Validation, and Support activities to meet the technology requirements of our clients. Your role will be crucial in maintaining high levels of service satisfaction within the technology domain.Your typical day will include gathering detailed requirements and specifications from clients to understand their needs thoroughly. You will then translate these requirements into system specifications, playing a pivotal role in the overall estimation of work requirements. Providing accurate project estimations to Technology Leads and Project Managers will be an essential part of your responsibilities.Your contribution will be significant in developing efficient programs and systems that cater to the digital transformation journey of our clients. If you believe you possess the skills and expertise to assist clients in navigating their digital transformation journey, then this opportunity at Infosys is tailored for you. Your role will be integral in helping clients achieve their digital transformation goals., #J-18808-Ljbffr

Water Quality Analyst

• Prepare water and solid samples for laboratory analysis.
• Conduct water quality testing using manual titration and colorimetric methods.
• Ensure timely delivery of test results to stakeholders.
• Maintain laboratory housekeeping and organizational standards.
• Support initiatives to enhance laboratory efficiency.

• Degree in Environmental Science, Chemistry, or Chemical Engineering, with experience in water quality testing.
• Resourceful team player with excellent communication skills.
• Strong proficiency in MS Office and ability to work under pressure.

• Opportunity to develop analytical and problem-solving skills.
• Chance to work in a dynamic and supportive environment.

• Prepare water and solid samples for analysis
• Analyze water samples using manual titration, colorimetric methods, and advanced instrumentation such as TOC, flow injection analyzers, UV-spectrometers, and titrators
• Maintain ISO17025 certification

• Diploma in chemistry or chemical engineering
• Relevant experience in water testing internships

This role involves working in a laboratory setting, performing various tasks such as sample preparation and analysis of water and solid samples. As a successful candidate, you will have strong analytical skills, be able to work independently and as part of a team, and possess good communication skills.

• Prepare samples for analysis of water and solid samples
• Conduct thorough analyses using manual titration and colorimetric methods on water samples
• Maintain a clean and organized laboratory environment with emphasis on 5S principles
• Collaborate in the development of process improvement initiatives
• Deliver accurate sample results within the given timeframe and disseminate them to concerned associates efficiently

• Hold a Diploma in Environment, Chemistry, or Chemical Engineering with relevant experience in water testing
• Demonstrate resourcefulness, teamwork capabilities, self-motivation, and a positive attitude
• Possess effective communication skills and proficiency in MS Office applications
• Be adept at managing pressure and meeting tight deadlines

• Water Testing
• MS Office
• Process Improvement
• Laboratory Organization
• Titration
• Teamwork
• Chemical Engineering

• Conduct inspections on raw materials, intermediates, and finished products through sensory evaluation, physical assessments, and analytical testing to ensure compliance with established specifications and standards.
• Perform routine equipment checks, calibrations, and basic maintenance to ensure accuracy and reliability of test results.
• Assist in investigations and resolution of non-conformances, including handling customer complaints and rejected items (internal/external).
• Maintain cleanliness, safety, and good laboratory practices within the QC lab environment.
• Support implementation and continuous improvement of QA/QC processes and initiatives.
• Perform other ad-hoc duties assigned by supervisors.

Interested applicants may email resume to

Chooi Kelly (CEI Registration No: R )

Recruit Express Pte Ltd (EA: 99C4599)

We regret only shortlisted candidates will be contacted

• Oversee the implementation and maintenance of GMP and HACCP standards.
• Ensure compliance with local food regulations (e.g., SFA and GMP standards).
• Manage internal and external audits (e.g., regulatory bodies, customer audits).
• Review and update QA documentation, SOPs, and records regularly.

• Lead hazard analysis, food safety plans, and critical control point monitoring.
• Manage allergen control, traceability, and recall procedures.

• Supervise the QC team in performing inspections, sampling, and laboratory testing (microbiological, chemical, physical).
• Analyze trends from quality data and implement improvements.
• Approve incoming raw materials, in-process, and finished product quality.

• Train and mentor junior QA/QC staff on quality systems and food safety.
• Conduct regular staff training on hygiene, GMP, and process controls.

• Initiate and lead quality improvement projects (e.g., reducing customer complaints, process optimization).

• Degree/Diploma in Food Science, Food Technology, Microbiology, or related field.
• 5 years of QA/QC experience in the food manufacturing industry.
• Strong knowledge of HACCP and GMP standards.
• Experience with audits, documentation control, and risk assessment.
• Excellent communication, leadership, and problem-solving skills.

Overview

MiRXES is a Singapore-headquartered molecular diagnostic company with R&D, manufacturing, and clinical lab operations in Singapore, USA, Japan, and China. We specialize in microRNA technologies and the development, manufacturing, and provision of diagnostic test kits and clinical services. Our mission is to enable early disease detection and provide insights for better patient care by harnessing the power of microRNA to augment traditional testing. Our vision is to be the world’s leading developer and provider of accurate, actionable, and affordable microRNA-powered diagnostic tests.

Job Location: 2 Tukang Innovation Grove, JTC MedTech Hub, Singapore

The QC Specialist will work as part of the Quality team, supporting day-to-day QC operations and maintaining accurate and detailed records of all the assigned tasks. This role involves inspecting products at various stages of the manufacturing process, including incoming raw materials, intermediates, in-process materials and finished goods. This person will also participate in investigations of nonconforming products and assist in implementing corrective actions arising from these inspections.

• Perform routine QC testing of incoming raw materials, in-process materials and finished goods.
• Plan and schedule daily routine and ad hoc QC runs assigned by line manager.
• Evaluate data and generate reports, highlighting any deviations from standard operating procedures (SOPs).
• Raise nonconformance for failures observed during QC runs.
• Support troubleshooting and investigation of nonconformance to determine root causes.
• Draft and revise QC work instructions as required.
• Support validation and stability studies for lab development and Diagnostic products, when necessary.
• Perform general laboratory support activities, including housekeeping, equipment maintenance, document archival, and inventory tracking of laboratory reagents, etc.
• Contribute to the continuous improvement of laboratory procedures and processes to ensure compliance with GMP requirements.
• Apply Good Documentation Practices (GDP) to all records to ensure traceability, transparency, and audit readiness.
• The tasks and responsibilities listed are essential to the role, however, reasonable accommodations may be made to support additional responsibilities based on evolving business needs.

• Degree/ Diploma in Biomedical Science, Biotechnology, Molecular Biology, Biochemistry, Life Science related courses or equivalent.
• Knowledge and hands-on experience with qPCR, including operation of qPCR machines will be an advantage.
• Proficient in using standard laboratory equipment such as pipettes, centrifuges, etc.
• Familiar with basic laboratory procedures; experience in assay-based workflows and QC testing is an advantage.
• Able to work independently with minimal supervision, as well as collaboratively with cross-functional teams.
• Excellent organizational and time management skills.
• Demonstrate a high degree of initiative and ownership.
• Possess a positive, proactive and willing-to-learn attitude.
• Strong interpersonal and communication skills.
• Basic computer competency, including proficiency in Microsoft Office applications.
• 2-3 years of relevant experience in quality control, preferably within the medical device manufacturing industry.
• Good understanding of Good Documentation Practices (GDP) and current Good Manufacturing Practices (cGMP) is preferred.

This position is based in Singapore.

We appreciate your interest in the above-mentioned position, however, only shortlisted candidates will be contacted.

The Quality Inspector is responsible for ensuring the quality of incoming materials, in-process components, and finished products through detailed inspection and testing. This role ensures that all products meet quality standards throughout the manufacturing process, from receipt of components to final product delivery

Incoming Quality Control:

• Inspect and verify incoming materials and components for micro assembly and PCBA against specifications and quality standards.

• Ensure proper documentation and traceability of incoming materials.

In-Process Quality Control:

• Monitor and inspect the micro assembly and PCBA assembly process to ensure in process quality control are in compliance according to standards.

• Perform in-process testing to detect defects early and minimize waste or rework.

Outgoing Quality Control:

• Inspect and test finished products before shipment to ensure they meet specifications, functionality, and visual standards.

• Conduct final functional and visual inspections to ensure product readiness.

Defect Identification & Reporting:

• Identify and document quality issues, defects, and deviations from standards during incoming, in-process, and outgoing inspections.

• Work with the production team to resolve issues and implement corrective actions.

Documentation & Compliance:

• Maintain accurate records of inspections, test results, and non-conformance reports.

• Ensure compliance with industry standards (IPC, ISO) and company quality policies.

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