20 Site Supervision jobs in Singapore

Description

Company description: Changi Airport Group (CAG) is the manager of Singapore Changi Airport, a leading air hub in Asia and one of the world's most awarded airports. As airport manager, CAG performs the key functions of airport operations, air hub development, retail and commercial activities, infrastructure development and airport emergency services. CAG also manages Seletar Airport, and through its subsidiary, Changi Airports International, it takes Changi's presence beyond Singapore's shores through consultancy projects and investments in foreign airports. Come join us today! Job description: As part of the Changi East Safety function, you will join the team responsible for ensuring that construction works and related activities are conducted safely in compliance with aerodrome safety, workplace safety & health (WSH) and site operations compliance and requirements. The team ensures safety by leveraging various means, ranging from culture promulgation to the development and deployment of digital interventions. Job Description: Assist in managing effective safety management systems for T5 development works. Manage projects and explore the adoption of technology related to safety and operations, including but not limited to identify potential gaps to safety & operational requirements contributing to the timely completion of T5 works. Drive collaboration to maintain safety and operations procedures, facilitate consensus building amongst stakeholders whenever there are differing requirements, organise safety trainings, and conduct safety evaluations for construction tenders. Serve as the secretariat for meetings with stakeholders to achieve key milestones. This includes but not limited to setting meeting agendas, performance reporting, compiling safety data for trend analysis, and review risk assessments. Job Requirements: Degree in any discipline with at least 1-3 years of relevant working experience with large corporations or government agencies (preferably in Safety Management, or a related field). Possess drive, initiative, meticulous and able to multi-task effectively in a dynamic and fast-paced work environment. Strong communication skills and the ability to work collaboratively with internal and external stakeholders at all levels. This is a contract position #J-18808-Ljbffr Industry

Other Category

Management & Operations Sub Category

Operations & Business Administration

Production Supervisor

Location: Sembawang
Working Days: 5.5 days A Week (44 hrs/week)
Working hours : 8am – 5pm (Mon-Fri) and 8am – 12pm (Sat)
Salary : $3,000 - $4,500 (Based on market rate, subject to individual’s qualification & experience)

Overview:

We are a public-listed company that specialises in the manufacturing of steel prefabricated reinforcement for the construction industry. We are seeking suitably qualified personnel to join our team.

Responsibilities:

• Supervise and monitor progress of bar bending activities on the production shopfloor.
• Read and interpret drawings, bar bending schedules and shop drawings.
• Ensure timely completion of rebar cutting and bending works in accordance with approved drawings.
• Resolve all site issues related to production, quality and safety matters.
• Practice advance planning and manage critical activities involving materials, manpower and equipment.
• Conduct regular checks to ensure quality compliance and that all works are executed according to approved drawings.
• Ensure that production activities comply with safety and quality standards at all times.

Requirements:

• Diploma in any engineering field
• Preferably with relevant experience in full-time production supervision
• Knowledge of safety management is preferred
• WSH Certification for supervisory or lifting supervision will be an added advantage

WhatsApp: (Shermaine)

Siah Sze Ming Reg No: R24125414

The Supreme HR Advisory Pte Ltd EA No: 14C7279

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Our client is seeking an Engineering Assistant (QC) to join their team! About Our Client

Our client is a leading manufacturer of high-quality electronic components. With a strong focus on innovation and customer satisfaction, they have built a reputation for delivering reliable and efficient solutions across various industries. Their dedicated team of professionals is committed to driving success and providing exceptional experiences for their customers. Join a company that values innovation and excellence in the electronic components sector.

What you'll be doing?

Verification and calibration: Perform verification of correlation standards and calibrate inspection, measuring, and test equipment to ensure accuracy.

System maintenance: Assist in maintaining the correlation and calibration system, keeping it up-to-date and efficient.

Liaison and communication: Work closely with the Head office on correlation and calibration issues, and collaborate with external service providers to resolve technical challenges.

Data management: Assist in data collection and analysis to support quality assurance processes.

Continuous improvement: Actively participate in projects aimed at enhancing processes and systems.

Quality compliance: Upkeep and improve QA lab systems to ensure compliance with quality management standards.

Technical testing: Conduct electrical measurements, Destructive Physical Analysis (DPA), and Board Flex tests on critical products, preparing reports as needed.

Knowledge sharing: Conduct on-the-job training for trainees, helping to develop the next generation of quality professionals.

Who are they looking for?

Educational background: Diploma Holder or Nitec in Electronic/Electrical Engineering or equivalent, ready to apply your knowledge in a practical setting, entry level is welcomed.

Experience: 2 to 3 years of relevant working experience in a manufacturing/Lab environment is advantageous, but not essential for the right candidate.

Technical skills: Proficiency in Microsoft Excel to support data analysis and reporting tasks.

Positive attitude: A willingness to learn and a positive mindset to tackle new challenges and grow in your role.

Other Information

Working Day: Mon to Fri, 8.15am to 5.15pm

Why you should consider this opportunity?

Our client offers an attractive remuneration package and other benefits, such as:

Transport pick-up from Bedok MRT station

13 days of Annual Leave

How to apply

Ready to join this role? Click Apply now to submit your resume and share your availability and expected salary with us!

We value diversity and encourage candidates from all backgrounds to apply for this exciting opportunity.

All information received will be kept strictly confidential and will be used only for employment-related purposes.

Low Jia Yi | R25127265

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Description

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Title: Supervisor, Quality Control, Jurong

Requisition ID: 70089

Location:Singapore, Singapore, SG

Department: Quality

Description:At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?

There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.

We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.

Job Summary

In this role, the QC Shift Lead will support the QC supervisor to ensure safe, compliant, and efficient operations in the Quality Control department. He/she will manage directly and closely support the quality inspectors in all areas.He/she will assist QC Manager to build-up a team of competent QC inspector to achieve consistent compliance and timely execution of tasks.He/she will monitor and control the daily activities of quality inspection, testing, documentation review.Carry out QC tasks/ inspections when required, to support the team.Responsible for Safety, accountable for adherence to procedures, quality and schedules on assigned shifts; promote effective team member/Company relations to help improve team engagement, customer service and Company profits.

Essential Duties and Responsibilities

• Supervise shift personnel in the quality control department consistent with high safety and quality standards.
• Troubleshoot problems arising on the shop floor in conjunction with quality standards with the appropriate engineering support from Quality Engineering functions
• Maintain close observation of quality requirements to keep quality management informed of status and, when needed, initiate the necessary steps to conform to schedule / staffing requirements.
• Promote and support site initiatives including quality safety programs, lean initiatives, training programs, and consistently interpret and apply all policies, practices and procedures among plant team members.
• Recommend and implement measures to motivate team members and to encourage employees to recommend ways to improve process, quality, safety and efficiency.
• Routinely evaluate team member performance and identify training needs. Coach and counsel team members for performance, attendance and behavior. Participate in the resolution of team members relations issues.
• Review and approve work time in the appropriate timekeeping system. Maintain and verify accuracy of the hours each team member has worked.
• Works independently to identify Quality issues, initiate nonconformance reports, and recommend corrective actions
• Determine product acceptability by performing various types of inspections and measurements utilizing varying laboratory equipment and taking care of valid calibration (internal and external)
• Create, utilize, and maintain testing result forms
• Develop sampling plans and activities, as required
• Authoring of quality notifications such as deviations and OOS (visual and dimensional)
• Support review of batch production records and perform review, approval, and release of product and materials within the inventory management/ERP system
• Ensures compliance with quality system documents, cGMPs, ISO standards and FDA regulations.
• Work with technical staff in performing root cause failure analysis and implementing corrective and preventive actions to eliminate recurrence.
• Manage the team’s performance, conduct performance 1 to 1’s, support recruitment, training and development plans while addressing any issues that arise in a timely manner
• Liaise with internal and external customers and other departments as appropriate.
• Ensure that the QC inspection conducted are performed according to relevant procedures and data reported in compliance with data integrity principles
• Act as a central point of communication for all departments in respect to product quality issues on the shop floor and ensure that these are escaladed appropriately.
• Other duties as assigned

Additional Responsibilities

• Participate in special project teams as assigned.
• Performs other duties as assigned based on business needs.
• Conforms with and abides by all laws, regulations, safety rules, policies, and work procedures, and all instructions.
• Exhibits regular, reliable, punctual and predictable attendance.

Education

• Associate's Degree Associate's Degree in Technical or Engineering required or
• Bachelor's Degree Degree in Technical or Engineering preferred

Work Experience

• Minimum 5 years Previous experience in Quality Assurance/Quality Control required and
• Experience in FDA regulated environment, pertinent to ISO 13485 preferred and

Preferred Knowledge, Skills and Abilities

• Must be familiar and proficient with computers and various software programs such as Microsoft Word, Microsoft Excel, Master-control, SAP
• Able to comply with the company’s safety policy at all times
• Able to comply with the company’s quality policy at all times.
• Support and contribute to Lean Sigma programs and activities towards delivery of the set target
• Leadership experience in leading teams of 10-15 people preferred

License and Certifications Travel Requirements

5%: Up to 13 business days per year

Physical Requirements

Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.

Additional Requirements

• Adaptable to changes in the work environment, manage competing demands and deal with frequent change, delays, or unexpected events.
• Maintain high attention to detail, accuracy, and overall quality of work.
• Effectively communicate and interface with various levels internally and with customers.
• Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description
• Performing the duties of this job involves the employee walking, standing on concrete floor, sitting for extended periods, lifting of cartons, containers, or bags of product, using hands and fingers to touch or feel materials or products, and listening for audible tones of equipment. This requires that the individual have normal hearing ability. The employee must be able to maintain concentration and visual acuity on tasks for extended periods.
• The employee must perform visual inspection of product, color standards, raw materials, and graphics. Specific vision abilities required to perform these tasks include close vision, color vision, peripheral vision, depth perception, and the ability to focus when viewing items through magnification. Required to work 40 hours a week and some overtime.

West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in orderto apply to West, please send an email to . Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening and/or a pre-employment drug screening.

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Industry

Biotech, Pharma & Chemistry

Category

Management & Operations

Sub Category

Quality Management & Operations

Description

Press Tab to Move to Skip to Content Link Select how often (in days) to receive an alert: Title: Supervisor, Quality Control, Jurong

Requisition ID: 70089 Location:Singapore, Singapore, SG Department: Quality Description:At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future? There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families. We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts. Job Summary

In this role, the QC Shift Lead will support the QC supervisor to ensure safe, compliant, and efficient operations in the Quality Control department. He/she will manage directly and closely support the quality inspectors in all areas.He/she will assist QC Manager to build-up a team of competent QC inspector to achieve consistent compliance and timely execution of tasks.He/she will monitor and control the daily activities of quality inspection, testing, documentation review.Carry out QC tasks/ inspections when required, to support the team.Responsible for Safety, accountable for adherence to procedures, quality and schedules on assigned shifts; promote effective team member/Company relations to help improve team engagement, customer service and Company profits. Essential Duties and Responsibilities

Supervise shift personnel in the quality control department consistent with high safety and quality standards. Troubleshoot problems arising on the shop floor in conjunction with quality standards with the appropriate engineering support from Quality Engineering functions Maintain close observation of quality requirements to keep quality management informed of status and, when needed, initiate the necessary steps to conform to schedule / staffing requirements. Promote and support site initiatives including quality safety programs, lean initiatives, training programs, and consistently interpret and apply all policies, practices and procedures among plant team members. Recommend and implement measures to motivate team members and to encourage employees to recommend ways to improve process, quality, safety and efficiency. Routinely evaluate team member performance and identify training needs. Coach and counsel team members for performance, attendance and behavior. Participate in the resolution of team members relations issues. Review and approve work time in the appropriate timekeeping system. Maintain and verify accuracy of the hours each team member has worked. Works independently to identify Quality issues, initiate nonconformance reports, and recommend corrective actions Determine product acceptability by performing various types of inspections and measurements utilizing varying laboratory equipment and taking care of valid calibration (internal and external) Create, utilize, and maintain testing result forms Develop sampling plans and activities, as required Authoring of quality notifications such as deviations and OOS (visual and dimensional) Support review of batch production records and perform review, approval, and release of product and materials within the inventory management/ERP system Ensures compliance with quality system documents, cGMPs, ISO standards and FDA regulations. Work with technical staff in performing root cause failure analysis and implementing corrective and preventive actions to eliminate recurrence. Manage the team’s performance, conduct performance 1 to 1’s, support recruitment, training and development plans while addressing any issues that arise in a timely manner Liaise with internal and external customers and other departments as appropriate. Ensure that the QC inspection conducted are performed according to relevant procedures and data reported in compliance with data integrity principles Act as a central point of communication for all departments in respect to product quality issues on the shop floor and ensure that these are escaladed appropriately. Other duties as assigned Additional Responsibilities

Participate in special project teams as assigned. Performs other duties as assigned based on business needs. Conforms with and abides by all laws, regulations, safety rules, policies, and work procedures, and all instructions. Exhibits regular, reliable, punctual and predictable attendance. Education

Associate's Degree Associate's Degree in Technical or Engineering required or Bachelor's Degree Degree in Technical or Engineering preferred Work Experience

Minimum 5 years Previous experience in Quality Assurance/Quality Control required and Experience in FDA regulated environment, pertinent to ISO 13485 preferred and Preferred Knowledge, Skills and Abilities

Must be familiar and proficient with computers and various software programs such as Microsoft Word, Microsoft Excel, Master-control, SAP Able to comply with the company’s safety policy at all times Able to comply with the company’s quality policy at all times. Support and contribute to Lean Sigma programs and activities towards delivery of the set target Leadership experience in leading teams of 10-15 people preferred License and Certifications

Travel Requirements

5%: Up to 13 business days per year Physical Requirements

Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time. Additional Requirements

Adaptable to changes in the work environment, manage competing demands and deal with frequent change, delays, or unexpected events. Maintain high attention to detail, accuracy, and overall quality of work. Effectively communicate and interface with various levels internally and with customers. Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description Performing the duties of this job involves the employee walking, standing on concrete floor, sitting for extended periods, lifting of cartons, containers, or bags of product, using hands and fingers to touch or feel materials or products, and listening for audible tones of equipment. This requires that the individual have normal hearing ability. The employee must be able to maintain concentration and visual acuity on tasks for extended periods. The employee must perform visual inspection of product, color standards, raw materials, and graphics. Specific vision abilities required to perform these tasks include close vision, color vision, peripheral vision, depth perception, and the ability to focus when viewing items through magnification. Required to work 40 hours a week and some overtime. West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in orderto apply to West, please send an email to . Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening and/or a pre-employment drug screening. #J-18808-Ljbffr Industry

Biotech, Pharma & Chemistry Category

Management & Operations Sub Category

Quality Management & Operations

Responsibilities

• Support the Solution Styrene Butadiene Rubber (SSBR) operation by conducting analytical testing for product quality control, verification, audit, investigation and troubleshooting.
• Perform calibration, maintenance, troubleshooting and training of lab instruments (GC, HPLC, GPC, FTIR, KF Titrators, Viscometers and others).
• Review and update Quality and Safety documents, such as Work Instructions, Risk Assessments and Forms.
• Carry out lab operation duties such as inventorising, chemical preparation, safety and facility checks, 5S, and housekeeping.
• Participate in continuous improvement efforts in the areas of Safety, Quality, Digitalization and Operation efficiency.

Requirements

• Diploma in Chemistry/ Chemical Science/ Chemical Engineering or any equivalent discipline
• At least 1 year of QC, Laboratory experience in petrochemical industry
• Strong understanding of formulation chemistry and raw materials.
• Detail-oriented, good problem-solver, team player with strong communication skills.

All Successful candidates can expect a very competitive remuneration package and a comprehensive range of benefits.

Please email your resume in a detailed Word format to

We regret that only shortlisted candidates will be notified

People Profilers Pte Ltd

20 Cecil St, #08-09, PLUS Building Singapore 049705

DID: 6950 9725

Georgez Josiah LIM

License Number: 02C4944
Registration Number : R1108994

People Profilers Pte Ltd (People Profilers) has entered into a Partnership Recruitment Collaboration with Employment and Employability Institute Pte Ltd (e2i), to extend the support of hiring beyond e2is resources to broaden the reach of jobseekers.

This is in partnership with the Employment and Employability Institute Pte Ltd (e2i).

e2i is the empowering network for workers and employers seeking employment and employability solutions. e2i serves as a bridge between workers and employers, connecting with workers to offer job security through job-matching, career guidance and skills upgrading services, and partnering employers to address their manpower needs through recruitment, training, and job redesign solutions. e2i is a tripartite initiative of the National Trades Union Congress set up to support nation-wide manpower and skills upgrading initiatives. By applying for this role, you consent to People Profilerss PDPA and e2is PDPA ( ).

Please be informed that the personal data you provided by way of your job application to People Profilers will be collected, used and disclosed by or on behalf of People Profilers to determine or investigate your suitability, eligibility or qualifications for employment with People Profilers and/or its Clients and manage your application for employment with People Profilers and/or its clients, including identifying you as a potential candidate for future suitable positions and/or notifying you of any such positions, either existing or in the future.

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Position Summary

QA Engineer (Process Quality Control) is responsible to develop & deploy inspection procedures to ensure conformance of material to be released. Candidates with experience in semiconductor manufacturing environment are encouraged to apply for this position.

Responsibilities

• Responsible for backend semiconductor packaging processes which ball drop, bumping, singulation, backgrind and mounting.
• Effectively providing engineering support in order to meet production output, product quality, efficiency, productivity, yield, cycle time and safety requirements.
• Responsible to analyse the process data and identify improvement actions and work on the improvement.
• Drive permanent solutions to resolve chronic process and quality issues.
• Responsible to evaluate new product/material/process during the pilot run and ensure process readiness.
• Responsible for the relevance of the Work Instructions, Control Plan, FMEA & Process Control documents.
• Responsible to prepare the line for internal & external audits and the follow-up actions.
• Any other ad-hoc duties as assigned.

Requirements

• Bachelor’s Degree in Engineering (Mechanical, Electrical, Materials, Chemical, or related field).
• Prior experience in semiconductor packaging processes (ball drop, bumping, singulation, backgrind, mounting) would be advantageous.
• Experience in process engineering, yield improvement, and quality control.
• Proficiency in data analysis and statistical process control (SPC).
• Familiarity with Failure Mode and Effects Analysis (FMEA), Control Plan, and Process Control documentation.
• Hands-on experience with new product/material/process evaluations.
• Ability to work in a fast-paced manufacturing environment.

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QA Engineer (Process Quality Control) is responsible for developing and deploying inspection procedures to ensure the conformance of materials to be released. Candidates with experience in a semiconductor manufacturing environment are encouraged to apply for this position.

Responsibilities

1. Responsible for backend semiconductor packaging processes such as ball drop, bumping, singulation, backgrind, and mounting.
2. Provide engineering support to meet production output, product quality, efficiency, productivity, yield, cycle time, and safety requirements.
3. Analyze process data to identify improvement actions and work on implementing improvements.
4. Drive permanent solutions to resolve chronic process and quality issues.
5. Evaluate new products, materials, and processes during pilot runs to ensure process readiness.
6. Maintain the relevance of Work Instructions, Control Plans, FMEA, and Process Control documents.
7. Prepare the line for internal and external audits and follow-up on corrective actions.
8. Perform any other ad-hoc duties as assigned.

Requirements

1. Bachelor’s Degree in Engineering (Mechanical, Electrical, Materials, Chemical, or related field).
2. Experience in semiconductor packaging processes (ball drop, bumping, singulation, backgrind, mounting) is advantageous.
3. Experience in process engineering, yield improvement, and quality control.
4. Proficiency in data analysis and statistical process control (SPC).
5. Familiarity with FMEA, Control Plan, and Process Control documentation.
6. Hands-on experience with new product/material/process evaluations.
7. Ability to work in a fast-paced manufacturing environment.

Seniority level

• Entry level

Employment type

• Full-time

Job function

• Engineering and Quality Assurance

Industries

• Semiconductors and Manufacturing

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We are seeking qualified and highly driven professionals to join our Quality Control Team.You will be required to support the Head of Quality Control in all aspects of operational/compliance audits/reviews in our office. This is to ensure our office complies with the firm’s system of quality management designed to comply with professional standards and regulatory and legal requirements.

Responsibilities

• Plan and conduct risk assessments and quality controls reviews to ensure compliance of all statutory, regulatory requirements and internal compliance requirements.
• Analyse and identify quality control gaps and validate that controls are operating effectively and timely.
• Provide/suggest refinements to improve controls and enhance quality control standards within the firm’s service lines and practices.
• Conduct independent reviews of audit engagements before audit opinions are signed.
• Carry out root cause analysis and monitor effectiveness of action plans to address quality and risk areas of weaknesses.
• Train, coach, develop and cultivate technical competencies to ensure capability of designated employees to maintain and comply with quality standards.
• Prepare and collate information/reports for regulatory and internal reviews and to handle any related coordination work.

Requirements

• Bachelor’s Degree in Accountancy or equivalent
• Minimum 5-8 years experience in an audit role in a large international or professional services firm.
• Experienced in quality reviews and/or internal audits preferred.
• Able to work independently and possess strong project management and analytical skills with the ability to work within a team in a fast-paced environment.
• Excellent presentation, written and verbal communication skills to communicate across all levels of staff and management.

For further information, and to apply, please visit our website via the “Apply” button below. #J-18808-Ljbffr