Total 758 construction quality control job vacancies in Quality Assurance / Control category

JOB RESPONSIBILITIES:

• Review the Associated Part Processing Method (APPM) & Job Instruction Sheet (JIS) and ensure to meet the Engineering Print requirements
• Review the Tolerance Chart and ensure to meet the final requirements of the component upon stock removal.
• Review Inspection Plans, Inspection Gauges, Equipment, Methods & Techniques.
• Prepare & review First Article Inspection (FAI) Report Forms Ballooned E/P as per AS9102.
• Design the gauge, to meet the process requirement.
• Assist in ordering new Gauges.
• Preparing Document of FMEA, Control Plan, and Process Flow Chart.
• Preparing PPAP.

REQUIREMENTS:

• Minimum Diploma holder in Engineering
• Candidate with Quality Background in Precision Engineering
• Able to use all types of standard & specialize gauges (CMM) and good judgment when applying during inspection planning
• Tool and gauge planning
• Good knowledge in GD& T and interpretation
• Able interpret engineering print & the specifications
• Knowledge in gauge designing
• PPAP & FAI documentation
• Exposure to modeling & drafting in NX

Position summary

Act as a technical expert in healthcare quality and regulatory analytics. Combine advanced quantitative analysis, data engineering, and quality system expertise to build stakeholder-specific reporting, develop AI-enabled quality tools, and integrate/manage third-party quality applications to support compliance, continuous improvement, and executive decision-making.

Key responsibilities (primary)

• Perform advanced quantitative data analysis: build statistical and machine learning models for trend detection, root-cause analysis, forecasting, anomaly detection, and risk stratification

• Design, build, and maintain stakeholder-specific dashboards and reports (executive, regulatory) using Power BI tools and data visualization best practices; deliver actionable insights and data storytelling.

• Develop and maintain quality tools and automations using AI/ML/LLM technologies (NLP for document classification/summarization, automated quality checks,

predictive analytics, chat assistants for SOP/QMS guidance).

• Lead integration and lifecycle management of third-party quality software: requirements gathering, vendor coordination, configuration, data integration, testing, release coordination, and ongoing support.

• Utilize current and emerging technologies in evaluating trends to business models and healthcare quality processes

• Develop insights and translate information into actionable initiatives to ensure business outcomes

• Lead and support projects through the application of technical expertise including conceptualization, planning, design, implementation and support of quality assurance processes, systems, and quality technology solutions

• Evaluate and monitor healthcare quality processes and systems to identify areas for continuous improvement and transformation ensuring global excellence

• Initiate and lead the development of reports for key stakeholders, including executive management, using data storytelling and visualization.

• Develop and execute tools to enhance services and deliver training for internal customers or vendors on analytics outputs, tools, and integrated systems.

• Gather and consolidate regulatory and business requirements into convert them into technical specifications and implement monitoring to ensure ongoing compliance with company’s internal policies and relevant regional and local regulations.

• Develop and maintain data validation, models, and metadata; routinely assess model performance and recalibrate as required.

• Lead end-to-end analytics projects: planning, stakeholder alignment, implementation, and post-implementation reviews; document methods and SOPs.

• Support audit readiness and provide analytics-driven evidence for regulatory submissions, inspections, and internal quality reviews.

• Identify opportunities for process improvement and automation in quality workflows, pilot new technologies and scale successful solutions.

Additional responsibilities (as needed)

• Provide subject-matter expertise for cross-functional programs and global initiatives.

• Manage vendor relationships and service-level expectations for third-party tools.

• Participate in career progression and mentoring for junior analysts.

Required skills and experience

• Bachelor's degree in Statistics, Data Science, Biostatistics, Engineering, Computer Science, Information Technology, Healthcare Analytics, or related field (or equivalent experience).

• Strong quantitative and statistical skills; proficiency in data science libraries and tools

• Experience building dashboards and visualizations with tools such as Power BI, Tableau, Looker, or equivalent.

• Hands-on experience integrating and managing third-party quality/GxP systems (MasterControl, Synthesis, ServiceNow) or similar QMS/issue tracking platforms.

• Experience working with cloud platforms, databases (SQL, NoSQL), ETL tools, and APIs.

• Practical experience applying AI/ML and prompt engineering for LLMs to automate quality processes, extract insights from unstructured documents, or create assistant workflows.

• Strong data validation, data modeling, and data governance understanding.

• Excellent communication and data storytelling skills; able to translate technical findings into concise recommendations for executives.

• Experience in a regulated environment (healthcare, life sciences, medical devices, or similar) strongly preferred.

• Demonstrated ability to work cross-functionally and manage vendor/IT relationships.

Preferred

• Certifications in data analytics, machine learning, or quality management.

• Prior experience with global operations or multi-regional regulatory frameworks.

Level expectations and experience guidelines

• 3-4 years relevant experience; independently manages projects and provides expert input, recognized expert, leads complex programs with high autonomy.

Core competencies

• Analytical thinking, accuracy, attention to detail, numerical skills.

• Planning and organizing, project management, stakeholder alignment.

• Statistical knowledge, data modeling, visualization skills, automation

• Vendor and cross-functional collaboration, training and documentation abilities.

Technical requirements

• Proficiency with Microsoft Office and web-based applications.

• Familiarity with automation and orchestration tools; experience deploying AI/ML models into production.

• Language: strong written and spoken English.

Compliance and other

• Ensure ongoing compliance with company processes, regional/local legislation, and external regulations.

• May be required to perform other duties as assigned; role can involve regional and global activities

Working Hours:

Mon to Fri 9am - 6pm ( 1 day hybrid )

Quality Operations Specialists must assist site management to oversee the quality system execution on the manufacturing and production areas at all times. The personnel are required to observe, document, discuss, and report quality adverse events related to the manufacturing of the product and are responsible to ensure highest quality and compliance of released batches. 

Responsibilities:

• Ensure that products manufactured meet approved company policies, processes and procedures

• Provide quality oversight of GMP manufacturing and manufacturing support, including technical operations, engineering, QC laboratory and supply chain activities.

• Review completed incoming material inspection packages, Batch Records, Manufacturing Logs, product changeover/line-clearance activities and administration of Quality Logs, e.g., QA Hold, QA tag out. 

• Release incoming material, process, and product batches.

• Participate in investigations arising out of non-compliance in incoming materials, QC testing, manufacturing processes, warehousing, and product.

• Participate in change management, including change coordinator and/or QA oversight roles to ensure change plan is managed and complies with applicable policies.

• Perform regular walk-through of manufacturing, engineering, warehouse and QC areas as required to ensure compliance is maintained at all times.

• Participate and support new product introduction, operation excellence projects and other tasks as assigned by management

About You:

• Bachelor Degree in a Natural Sciences (i.e. Biology, Chemistry), Engineering, Pharmacy or other relevant courses

• Minimum of 2 years of pharmaceutical, biopharmaceutical experience in Quality and/or Compliance (GxP) environment.

• Prior experience in setting up of electronic batch records is a plus.

• Ability to quickly know products and processes in order to assess quality issues

• Committed to quality and maintain a high standard of work at all times

• Demonstrates the highest levels of integrity and a strong work ethic

• Good knowledge of GxP requirements and regulations

• Good planning and scheduling skills

• Good communication and interpersonal skills both verbal and written

Duration: 6 months contract. (Option to renew/convert based on performance)

Job Overview

We are looking for a skilled and responsible Electrical Quality Assurance (QA) Technician for inspecting, testing, and verifying that electrical switchboards, panels, and associated components meet design specifications, safety standards, and quality requirements before they are shipped to customers.

Key Responsibilities

• In-Process Inspection: Perform inspections during the assembly of the switchboard, verifying proper installation of components, wiring, and adherence to electrical schematics.
• Final Inspection and Testing (FAT): Conduct final, detailed visual inspections, functional tests (e.g., operational checks of breakers, lights, and meters), and dielectric strength (high-pot, Mega, PI, SI, Injection Test) testing to ensure the switchboard is ready for service.
• Documentation and Reporting: Create, maintain, and update inspection reports, quality records, and non-conformity reports.
• Collaboration: Liaise with production, engineering, and sales teams to resolve quality issues and support project timelines.

Requirements

• Experience: 1-2 years of relevant experience in a QA/QC role, preferably in manufacturing.
• Technical Knowledge: Ability to read and interpret electrical wiring diagrams, CAD drawings, and schematics.
• Tools: Proficient in using hand tools, precision measuring tools, and electrical testing equipment.
• Soft Skills: Strong attention to detail, analytical skills for troubleshooting, and effective communication.

Job Description:

• In Charge of auditing and assessing the suitability of suppliers
• Responsible for initiating and managing project transfer
• Responsible for guiding and implementing improvement programs as well as negotiating and balancing capacity among suppliers
• Responsible for FA Inspection of casting and machining services
• In Charge of managing the foundries which include quality and delivery performance
• In charge of handling the non-conformance parts follow up
• Responsible for checking and monitoring suppliers to ensure delivery

Requirements:

• Min Diploma in Mechanical / Precision Engineering or relevant
• Min 5 years of experience in Oil & Gas industry with experience in Supplier Quality
• Oversea travelling is required

To submit your application, please apply online to apply@rn-care.com or call +(65) 6513 5697 for private and confidential discussion.

Your interest will be treated with the strictest of confidence. We regret that only shortlisted candidates will be notified or contacted.

RN Care Pte. Ltd
EA License No: 17C8900

• Basic $4000 to $6000 + Variable Bonus + Allowances
• Excellent Welfare and Benefits + Career progression
• Working location: West / Northeast (Both location available)
• Working hours: 8:30am – 5:30pm (Mon – Fri)
• Automation, Control, PLC Systemw

Job Responsibilities:

• Manage and implement automation projects from start to finish
• Develop software programs for control systems
• Conduct system maintenance, troubleshooting, and user training
• Work in diverse environments including process plant, vessels, and construction sites
• collaborate with cross functional teams to ensure successful project delivery

Requirements:

• Possess Diploma or Bachelor's Degree in Electrical & Electronic Engineering, Mechatronics, or related field
• Familiar with industrial automation system and control instrumentation
• 2 to 3 years of relevant working experience in industrial automation or control systems

Candidates are encouraged to apply this position via Apply Now button with the following information in the resume

• Work experiences and job responsibilities
• Current and Expected salary
• Reason for leaving
• Date of availability
• Education background

We regret that only shortlisted candidates will be contacted.

NG DIAUM YEE (R2198031)

EA Recruitment Pte Ltd

EA License No: 21C0492

Job Description:

• In Charge of auditing and assessing the suitability of suppliers
• Responsible for initiating and managing project transfer
• Responsible for guiding and implementing improvement programs as well as negotiating and balancing capacity among suppliers
• Responsible for FA Inspection of casting and machining services
• In Charge of managing the foundries which include quality and delivery performance
• In charge of handling the non-conformance parts follow up
• Responsible for checking and monitoring suppliers to ensure delivery

Requirements:

• Min Diploma in Precision Engineering or relevant
• Min 5 years of experience in Metal Machining industry with experience in QC/ Audit
• Extensive travelling is required

To submit your application, please apply online apply@rn-care.com or call +(65) 6513 5697 for private and confidential discussion.

Your interest will be treated with the strictest of confidence. We regret that only shortlisted candidates will be notified or contacted.

RN Care Pte. Ltd
EA License No: 17C8900

Position Overview 

The position of Specialist provides quality oversight on Supplier qualification & management and co-ordinates with central quality functions as needed. The role will ensure and maintain high standards of quality and compliance within our organization.   

Essential Functions and Responsibilities (includes, but are not limited to): 

The ​Associate/Specialist(P1/2)​, Supplier Quality is responsible to: 

• Acts as the subject matter expert for Supplier quality management engaging directly in internal and external quality/ regulatory audits and in the development and execution of any remediation actions that may be required.    
• Establish Quality/Change agreements between the company and suppliers, ensure content alignment through coordination with site SMEs, and manage the end-to-end approval workflow. 
• Update site SOPs to reflect the changes needed to achieve compliance with Quality Manual/ GDL requirements. 
• Manage and maintain Supplier related EDMS, where applicable. 
• Supervise and oversee Third Party Contractors, involved in the supplier qualification process where applicable. 
• Demonstrate the ability to independently solve problems that arise within job responsibilities and expectations. Able to organize information in a logical way and combine data and information frommultiple sources in new ways to determine causes of issues. 
• Apply appropriate knowledge of compliance requirements, HA and regulatory authority expectations and business intelligence to support development of and amendments to internal quality policies. 
• Track and manage CAPA commitments from supplier to avoid any overdue. 
• Drive collaboration and transformational culture change.   
• COMET QM System Support​ 
• Review, approve as well as provide support as site SME for COMET QM system updates 

Qualifications & Experience 

Bachelor’s degree in Science/ Life Science, Pharmaceutical Science, Engineering or proven relevant experience. 

300/P1 Specialist 

• 1-3 years of relevant experience in quality assurance in pharmaceutical manufacturing environment, supplying to highly regulated markets such as FDA and EMA. 
• Good knowledge and understanding of GMP and application of pharmaceutical regulatory requirements.

Personal Qualities 

• Leadership skills and ability to influence/collaborate with stakeholders at various levels. 
• Customer focus with strong business acumen and continuous improvement mindset. 
• Strategic and critical thinking mindset with a collaborative and problem-solving attitude. 
• Strong communication and interpersonal skills. 
• Ability to work effectively in a team-based environment. 

This is a career conversion program under Workforce Singapore (WSG) and candidates must meet the following criteria and are open to the following conditions:

• Singaporeans/Singapore PRs only
• PMETs/Mid-Careerist with no prior work experience in Biopharma industry are welcomed to apply
• Open to two years contract

WHAT YOU CAN EXPECT 

• Limitless opportunities across various areas in Manufacturing; well-structured career path  
• A state-of-the-art facility that delivers solution to its customers world-wide  
• Highly engaging team that aims to innovate the future