Quantity Surveyor (Façade- Curtain wall)
3 days
800+ Assistant Quantity Surveyor Jobs - November 2026 - Urgent Hiring - Page 24
Showing 887 jobs results for
"assistant quantity surveyor"
Senior Quantity Surveyor (Façade- Curtain wall)
3 days
Quantity Surveyor (Corporate fit-outs)
- Collaborate closely with the interior design team to review technical drawings and establish precise material take-offs.
2 days
Quantity Surveyor (Corporate fit-outs)
- Collaborate closely with the interior design team to review technical drawings and establish precise material take-offs.
10 days
Quantity Surveyor - Electrical (2 Positions)
- Corporate Office Team (Aljunied Area)
19 days
Quantity Surveyor Intern – Mechanical - Electrical
- Job Responsibilities:
21 days
Quantity Surveyor – Mechanical (Equipment, Piping ...
- Prepare quantity take-offs and BOQs for equipment, piping and structural works.
3 days
Quantity Surveyor - Electrical (2 Positions)
22 days
Quantity Surveyor - Electrical (2 Positions)
- Corporate Office Team (Aljunied Area)
23 days
Quantity Surveyor (Façade- Curtain wall)
19 days
Quantity Surveyor - Electrical (2 Positions)
- Corporate Office Team (Aljunied Area)
25 days
Quantity Surveyor - Electrical (2 Positions)
- Corporate Office Team (Aljunied Area)
28 days
Administrative Assistant (Construction - QS Department)
10 days
Administrative Assistant (Construction - QS Department)
- Quotation Preparation: Assist the QS in preparing quotations and maintaining quotation records.
10 days
Quantity Surveyor (ID Fit Out)
- Prepare tender documents, review terms and specifications, estimate BQ and project resources and timeline planning.
29 days
QS Manager
- Lead, supervise, mentor, and develop the Quantity Surveying team.
30+ days
Contracts Quantity Surveyor [SL]
8 days
Cost Manager-Senior Cost Manager (Quantity Survey Procurement)
- Hold the highest level of professional integrity and business ethics.
19 days
Assistant QAQC Manager (semiconductor construction)
3 days
QA-QC - Production Assistant
- Assist in implementing, maintaining, and improving the company's Food Safety Management System (FSMS).
2 days
F-B QA-QC Assistant | Up to $2.6K-AWS | 5.5 days | Boon Lay- JY
- Conduct hygiene inspections and quality checks on raw materials, in-process items and finished products.
2 days
QA-QC Assistant (Up to $3000, Paya Lebar, Pharmaceutical) #HJY
- Location: Paya LebarDuration: PermanentSalary: $2500 - $3000Working days and hours:- 5 days, Office Hours Job Description:- Prepare, review, revise and implement Standard Operating Procedures (SOPs) and other Quality Management System (QMS) documents in accordance with applicable GMP requirements.- Ensure compliance with GMP requirements and established company procedures.- Perform Quality Control (QC) activities, including sampling, arranging laboratory testing according to approved specifications, reviewing analytical/test reports and assessing test results for product disposition.- Support and/or perform batch/product release activities in accordance with approved specifications and procedures.- Manage and investigate Out-of-Specification (OOS), deviations, non-conformances and other quality-related issues, including root cause investigation and Implementation of appropriate CAPA.- Perform sampling and testing activities and coordinate with external testing laboratories where applicable.- Develop, review and maintain product specifications, test methods, analytical reports, Certificates of Analysis (COA) and related quality documents.- Plan and coordinate calibration activities in accordance with the Calibration Master Plan.- Plan, coordinate and perform process and equipment validation activities, including preparation and review of validation protocols and reports.- Manage stability studies, retention samples, change controls, document control and product technical files.- Conduct Product Quality Reviews (PQR) and quality risk assessments/management.- Manage the retention sample room and ensure proper storage, identification and traceability of retention samples.- Conduct Environmental Monitoring of production areas and review monitoring results to ensure compliance with established requirements.- Support new product formulation, product development and Research & Development (R&D) activities from a quality and regulatory perspective.- Conduct GMP training and participate in internal audits, including follow-up and closure of audit findings.- Conduct and/or participate in supplier, contract manufacturer and external audits.- Manage customer/product complaints, conduct investigations and propose appropriate CAPA and follow-up actions.- Support regulatory submissions, product registration and maintenance activities, including liaison with HSA and other relevant regulatory authorities regarding regulatory and quality matters.- Liaise with internal and external stakeholders to support and streamline the regulatory requirements and export of company products.- Maintain and continuously improve the company's QMS and ensure effective implementation of quality systems.- Perform any other duties or activities reasonably assigned by management.
2 days
QA-QC Assistant (Up to $3000, Paya Lebar, Pharmaceutical) #HJY
- Location: Paya LebarDuration: Contract - Permanent/Permanent Salary: $2500 - $3000Working days and hours:- 5 days, Office Hours Job Description:- Prepare, review, revise and implement Standard Operating Procedures (SOPs) and other Quality Management System (QMS) documents in accordance with applicable GMP requirements.- Ensure compliance with GMP requirements and established company procedures.- Perform Quality Control (QC) activities, including sampling, arranging laboratory testing according to approved specifications, reviewing analytical/test reports and assessing test results for product disposition.- Support and/or perform batch/product release activities in accordance with approved specifications and procedures.- Manage and investigate Out-of-Specification (OOS), deviations, non-conformances and other quality-related issues, including root cause investigation and Implementation of appropriate CAPA.- Perform sampling and testing activities and coordinate with external testing laboratories where applicable.- Develop, review and maintain product specifications, test methods, analytical reports, Certificates of Analysis (COA) and related quality documents.- Plan and coordinate calibration activities in accordance with the Calibration Master Plan.- Plan, coordinate and perform process and equipment validation activities, including preparation and review of validation protocols and reports.- Manage stability studies, retention samples, change controls, document control and product technical files.- Conduct Product Quality Reviews (PQR) and quality risk assessments/management.- Manage the retention sample room and ensure proper storage, identification and traceability of retention samples.- Conduct Environmental Monitoring of production areas and review monitoring results to ensure compliance with established requirements.- Support new product formulation, product development and Research & Development (R&D) activities from a quality and regulatory perspective.- Conduct GMP training and participate in internal audits, including follow-up and closure of audit findings.- Conduct and/or participate in supplier, contract manufacturer and external audits.- Manage customer/product complaints, conduct investigations and propose appropriate CAPA and follow-up actions.- Support regulatory submissions, product registration and maintenance activities, including liaison with HSA and other relevant regulatory authorities regarding regulatory and quality matters.- Liaise with internal and external stakeholders to support and streamline the regulatory requirements and export of company products.- Maintain and continuously improve the company's QMS and ensure effective implementation of quality systems.- Perform any other duties or activities reasonably assigned by management.
4 days
QA-QC Assistant (Up to $3000, Paya Lebar, Pharmaceutical) #HJY
- Location: Paya LebarDuration: Contract - Permanent/Permanent Salary: $2500 - $3000Working days and hours:- 5 days, Office Hours Job Description:- Prepare, review, revise and implement Standard Operating Procedures (SOPs) and other Quality Management System (QMS) documents in accordance with applicable GMP requirements.- Ensure compliance with GMP requirements and established company procedures.- Perform Quality Control (QC) activities, including sampling, arranging laboratory testing according to approved specifications, reviewing analytical/test reports and assessing test results for product disposition.- Support and/or perform batch/product release activities in accordance with approved specifications and procedures.- Manage and investigate Out-of-Specification (OOS), deviations, non-conformances and other quality-related issues, including root cause investigation and Implementation of appropriate CAPA.- Perform sampling and testing activities and coordinate with external testing laboratories where applicable.- Develop, review and maintain product specifications, test methods, analytical reports, Certificates of Analysis (COA) and related quality documents.- Plan and coordinate calibration activities in accordance with the Calibration Master Plan.- Plan, coordinate and perform process and equipment validation activities, including preparation and review of validation protocols and reports.- Manage stability studies, retention samples, change controls, document control and product technical files.- Conduct Product Quality Reviews (PQR) and quality risk assessments/management.- Manage the retention sample room and ensure proper storage, identification and traceability of retention samples.- Conduct Environmental Monitoring of production areas and review monitoring results to ensure compliance with established requirements.- Support new product formulation, product development and Research & Development (R&D) activities from a quality and regulatory perspective.- Conduct GMP training and participate in internal audits, including follow-up and closure of audit findings.- Conduct and/or participate in supplier, contract manufacturer and external audits.- Manage customer/product complaints, conduct investigations and propose appropriate CAPA and follow-up actions.- Support regulatory submissions, product registration and maintenance activities, including liaison with HSA and other relevant regulatory authorities regarding regulatory and quality matters.- Liaise with internal and external stakeholders to support and streamline the regulatory requirements and export of company products.- Maintain and continuously improve the company's QMS and ensure effective implementation of quality systems.- Perform any other duties or activities reasonably assigned by management.
6 days
F-B QA-QC Assistant | Up to $2.6K-AWS | 5.5 days | Boon Lay- JY
- Conduct hygiene inspections and quality checks on raw materials, in-process items and finished products.
7 days
QA-QC Assistant (Up to $3000, Paya Lebar, Pharmaceutical) #HJY
- Location: Paya LebarDuration: Contract - Permanent/Permanent Salary: $2500 - $3000Working days and hours:- 5 days, Office Hours Job Description:- Prepare, review, revise and implement Standard Operating Procedures (SOPs) and other Quality Management System (QMS) documents in accordance with applicable GMP requirements.- Ensure compliance with GMP requirements and established company procedures.- Perform Quality Control (QC) activities, including sampling, arranging laboratory testing according to approved specifications, reviewing analytical/test reports and assessing test results for product disposition.- Support and/or perform batch/product release activities in accordance with approved specifications and procedures.- Manage and investigate Out-of-Specification (OOS), deviations, non-conformances and other quality-related issues, including root cause investigation and Implementation of appropriate CAPA.- Perform sampling and testing activities and coordinate with external testing laboratories where applicable.- Develop, review and maintain product specifications, test methods, analytical reports, Certificates of Analysis (COA) and related quality documents.- Plan and coordinate calibration activities in accordance with the Calibration Master Plan.- Plan, coordinate and perform process and equipment validation activities, including preparation and review of validation protocols and reports.- Manage stability studies, retention samples, change controls, document control and product technical files.- Conduct Product Quality Reviews (PQR) and quality risk assessments/management.- Manage the retention sample room and ensure proper storage, identification and traceability of retention samples.- Conduct Environmental Monitoring of production areas and review monitoring results to ensure compliance with established requirements.- Support new product formulation, product development and Research & Development (R&D) activities from a quality and regulatory perspective.- Conduct GMP training and participate in internal audits, including follow-up and closure of audit findings.- Conduct and/or participate in supplier, contract manufacturer and external audits.- Manage customer/product complaints, conduct investigations and propose appropriate CAPA and follow-up actions.- Support regulatory submissions, product registration and maintenance activities, including liaison with HSA and other relevant regulatory authorities regarding regulatory and quality matters.- Liaise with internal and external stakeholders to support and streamline the regulatory requirements and export of company products.- Maintain and continuously improve the company's QMS and ensure effective implementation of quality systems.- Perform any other duties or activities reasonably assigned by management.
7 days
QA-QC Assistant (Up to $3000, Paya Lebar, Pharmaceutical) #HJY
- Location: Paya LebarDuration: Contract - Permanent/Permanent Salary: $2500 - $3000Working days and hours:- 5 days, Office Hours Job Description:- Prepare, review, revise and implement Standard Operating Procedures (SOPs) and other Quality Management System (QMS) documents in accordance with applicable GMP requirements.- Ensure compliance with GMP requirements and established company procedures.- Perform Quality Control (QC) activities, including sampling, arranging laboratory testing according to approved specifications, reviewing analytical/test reports and assessing test results for product disposition.- Support and/or perform batch/product release activities in accordance with approved specifications and procedures.- Manage and investigate Out-of-Specification (OOS), deviations, non-conformances and other quality-related issues, including root cause investigation and Implementation of appropriate CAPA.- Perform sampling and testing activities and coordinate with external testing laboratories where applicable.- Develop, review and maintain product specifications, test methods, analytical reports, Certificates of Analysis (COA) and related quality documents.- Plan and coordinate calibration activities in accordance with the Calibration Master Plan.- Plan, coordinate and perform process and equipment validation activities, including preparation and review of validation protocols and reports.- Manage stability studies, retention samples, change controls, document control and product technical files.- Conduct Product Quality Reviews (PQR) and quality risk assessments/management.- Manage the retention sample room and ensure proper storage, identification and traceability of retention samples.- Conduct Environmental Monitoring of production areas and review monitoring results to ensure compliance with established requirements.- Support new product formulation, product development and Research & Development (R&D) activities from a quality and regulatory perspective.- Conduct GMP training and participate in internal audits, including follow-up and closure of audit findings.- Conduct and/or participate in supplier, contract manufacturer and external audits.- Manage customer/product complaints, conduct investigations and propose appropriate CAPA and follow-up actions.- Support regulatory submissions, product registration and maintenance activities, including liaison with HSA and other relevant regulatory authorities regarding regulatory and quality matters.- Liaise with internal and external stakeholders to support and streamline the regulatory requirements and export of company products.- Maintain and continuously improve the company's QMS and ensure effective implementation of quality systems.- Perform any other duties or activities reasonably assigned by management.
8 days
QA-QC Assistant (Up to $3000, Paya Lebar, Pharmaceutical) #HJY
- Location: Paya LebarDuration: PermanentSalary: $2500 - $3000Working days and hours:- 5 days, Office Hours Job Description:- Prepare, review, revise and implement Standard Operating Procedures (SOPs) and other Quality Management System (QMS) documents in accordance with applicable GMP requirements.- Ensure compliance with GMP requirements and established company procedures.- Perform Quality Control (QC) activities, including sampling, arranging laboratory testing according to approved specifications, reviewing analytical/test reports and assessing test results for product disposition.- Support and/or perform batch/product release activities in accordance with approved specifications and procedures.- Manage and investigate Out-of-Specification (OOS), deviations, non-conformances and other quality-related issues, including root cause investigation and Implementation of appropriate CAPA.- Perform sampling and testing activities and coordinate with external testing laboratories where applicable.- Develop, review and maintain product specifications, test methods, analytical reports, Certificates of Analysis (COA) and related quality documents.- Plan and coordinate calibration activities in accordance with the Calibration Master Plan.- Plan, coordinate and perform process and equipment validation activities, including preparation and review of validation protocols and reports.- Manage stability studies, retention samples, change controls, document control and product technical files.- Conduct Product Quality Reviews (PQR) and quality risk assessments/management.- Manage the retention sample room and ensure proper storage, identification and traceability of retention samples.- Conduct Environmental Monitoring of production areas and review monitoring results to ensure compliance with established requirements.- Support new product formulation, product development and Research & Development (R&D) activities from a quality and regulatory perspective.- Conduct GMP training and participate in internal audits, including follow-up and closure of audit findings.- Conduct and/or participate in supplier, contract manufacturer and external audits.- Manage customer/product complaints, conduct investigations and propose appropriate CAPA and follow-up actions.- Support regulatory submissions, product registration and maintenance activities, including liaison with HSA and other relevant regulatory authorities regarding regulatory and quality matters.- Liaise with internal and external stakeholders to support and streamline the regulatory requirements and export of company products.- Maintain and continuously improve the company's QMS and ensure effective implementation of quality systems.- Perform any other duties or activities reasonably assigned by management.
9 days
QA-QC Assistant (Up to $3000, Paya Lebar, Pharmaceutical) #HJY
- Location: Paya LebarDuration: Contract - Permanent/Permanent Salary: $2500 - $3000Working days and hours:- 5 days, Office Hours Job Description:- Prepare, review, revise and implement Standard Operating Procedures (SOPs) and other Quality Management System (QMS) documents in accordance with applicable GMP requirements.- Ensure compliance with GMP requirements and established company procedures.- Perform Quality Control (QC) activities, including sampling, arranging laboratory testing according to approved specifications, reviewing analytical/test reports and assessing test results for product disposition.- Support and/or perform batch/product release activities in accordance with approved specifications and procedures.- Manage and investigate Out-of-Specification (OOS), deviations, non-conformances and other quality-related issues, including root cause investigation and Implementation of appropriate CAPA.- Perform sampling and testing activities and coordinate with external testing laboratories where applicable.- Develop, review and maintain product specifications, test methods, analytical reports, Certificates of Analysis (COA) and related quality documents.- Plan and coordinate calibration activities in accordance with the Calibration Master Plan.- Plan, coordinate and perform process and equipment validation activities, including preparation and review of validation protocols and reports.- Manage stability studies, retention samples, change controls, document control and product technical files.- Conduct Product Quality Reviews (PQR) and quality risk assessments/management.- Manage the retention sample room and ensure proper storage, identification and traceability of retention samples.- Conduct Environmental Monitoring of production areas and review monitoring results to ensure compliance with established requirements.- Support new product formulation, product development and Research & Development (R&D) activities from a quality and regulatory perspective.- Conduct GMP training and participate in internal audits, including follow-up and closure of audit findings.- Conduct and/or participate in supplier, contract manufacturer and external audits.- Manage customer/product complaints, conduct investigations and propose appropriate CAPA and follow-up actions.- Support regulatory submissions, product registration and maintenance activities, including liaison with HSA and other relevant regulatory authorities regarding regulatory and quality matters.- Liaise with internal and external stakeholders to support and streamline the regulatory requirements and export of company products.- Maintain and continuously improve the company's QMS and ensure effective implementation of quality systems.- Perform any other duties or activities reasonably assigned by management.
9 days
12 days