100+ Jsp Jobs - July 2026 - Urgent Hiring
Showing 192 jobs results for
"jsp"
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Manage Alert
SGD7,000 - SGD10,000 Per Month
Islandwide (Singapore)
- 6–9 years of experience in Java Full Stack Development
- Strong expertise in Java, Spring/Spring Boot,
- Proficiency in React.js/Angular and modern frontend technologies ...
Posted
7 days ago
SGD7,000 - SGD7,000 Per Month
Singapore
- 6–9 years of experience in Java Full Stack Development
- Strong expertise in Java, Spring/Spring Boot,
- Proficiency in React.js/Angular and modern frontend technologies ...
Posted
7 days ago
SGD9,000 - SGD9,000 Per Month
Singapore
- 6–9 years of experience in Java Full Stack Development
- Strong expertise in Java, Spring/Spring Boot,
- Proficiency in React.js/Angular and modern frontend technologies ...
Posted
7 days ago
RECRUIT EXPRESS PTE LTD
SGD2,500 - SGD2,500 Per Month
Singapore
- Welcome and assist customers in the showroom.
- Understand customer needs and collect customer details for follow-up.
- Maintain showroom appearance and ensure displays are well presented. ...
Posted
13 days ago
RECRUIT EXPRESS PTE LTD
SGD3,000 - SGD3,000 Per Month
Singapore
- Support HR Business Partners in HR operations, including recruitment, manpower planning, rewards strategies, performance management, and employee engagement.
- Collaborate with Shared Services team in the timely appointment, re-appointment, promotion, and transfer of research staff.
- Assist with onboarding and offboarding processes to ensure smooth transitions for all employees. ...
Posted
13 days ago
SGD1,800 - SGD1,800 Per Month
Singapore
- Perform picking & packing
- Prepare and pasting of barcode & storage
- To load and unloading items onto trolley and transport to different departments. ...
Posted
13 days ago
Undisclosed
Singapore
- All are welcome!
- Contact: schoolrelations@sp.edu.sg
- Parents & O- and N- level students ...
Posted
13 days ago
OMNIVISION TECHNOLOGIES SINGAPORE PTE. LTD.
SGD8,000 - SGD8,000 Per Month
Singapore
- Responsible for implementing ISP Algorithm into HW using Verilog, SystemVerilog and/or SystemC (High Level Synthesis)
- Define ISP HW Architecture based on product features and performance requirements, also with gate count and power estimation
- Verify Logic at ISP level and Digital System level ...
Posted
19 days ago
Recruit Express Pte Ltd
Undisclosed
Singapore
- Contribute to site activation by:
- Assisting/ with the site staff access to vendor systems
- Access reconciliation quarterly ...
Posted
3 days ago
SGD8,400 - SGD9,700 Per Month
Islandwide (Singapore)
- Industry/ Organization Type: Information Technology Consulting
- Position Title: Product Manager (Esp Data & AI Platform)
- Working Location: Pasir Panjang ...
Posted
2 days ago
Undisclosed
KL City
- Support the daily operations of the Atlassian Cloud Enterprise platform across the Würth Group.
- Handle incidents, service requests and user inquiries related to Jira, Jira Service Management and Confluence, including timely analysis, resolution, documentation and escalation where required.
- Configure and maintain projects, workflows, request types, permissions, dashboards, spaces and related platform settings across Jira, Jira Service Management and Confluence to support stable and efficient operations. ...
Posted
4 days ago
SGD5,000 - SGD5,000 Per Month
Singapore
- Support regional product launches and coordinate marketing activities across APAC markets.
- Plan and execute digital and offline marketing campaigns, working closely with local marketing and sales teams.
- Monitor campaign performance, lead generation, and customer engagement to improve marketing effectiveness. ...
Posted
6 days ago
Undisclosed
KL City
- Work with stakeholders to gather requirements and design planning solutions using o9, Kinaxis, OMP, Blue Yonder, RELEX, and other cloud-based planning solutions.
- Configure, customize, test and optimize planning platforms to meet client needs.
- Lead or participate in project phases including analysis, design, development, testing, deployment, and post-go-live support. ...
Posted
6 days ago
Undisclosed
KL City
- Work with stakeholders to gather requirements and design planning solutions using o9, Kinaxis, OMP, Blue Yonder, RELEX, and other cloud-based planning solutions.
- Configure, customize, test and optimize planning platforms to meet client needs.
- Lead or participate in project phases including analysis, design, development, testing, deployment, and post-go-live support. ...
Posted
7 days ago
Undisclosed
KL City
- Design, develop, and test large-scale, distributed custom software systems using modern technologies such as Node.js, Java, Kafka, and cloud platforms.
- Apply Agile development practices, including test automation, deployment automation, and CI/CD, to enhance delivery speed and product quality.
- Act as a subject matter expert and in-house consultant, providing guidance and resolution for complex technical issues. ...
Posted
14 days ago
Thermo Fisher Scientific
Undisclosed
Singapore
- Manage all clinical operational and quality aspects of allocated studies, of low to moderate complexity, in compliance with ICH GCP. In accordance to project specific requirements, may assume Clinical Study Manager (CSM) responsibilities on small and/or less complex projects.
- Develop clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan. Contribute to the development of the Master Action Plan (MAP) for providing clinical related documents. Ensure timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central). May participate in the design and development of CRFs, CRF guidelines, patient informed consent templates and other protocol specific documents as required. Collaborate with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meetings.
- Collaborate with the clinical team and other departments as needed to meet deliverables of the project. Regularly communicate with the team and lead team meetings to ensure that timelines, resources, interactions, and quality are maintained. Responsible for the implementation and training of standardized clinical monitoring processes within the study and according to corporate standard policies. Responsible for the timely archiving of documents and study materials for the department. ...
Posted
21 days ago
SGD8,400 - SGD8,400 Per Month
Singapore
- Industry/ Organization Type: Information Technology Consulting
- Position Title: Product Manager (Esp Data & AI Platform)
- Working Location: Pasir Panjang ...
Posted
8 days ago
SGD3,500 - SGD4,000 Per Month
Central
- Handle customer enquiries on product availability, pricing, and delivery schedules.
- Process sales orders, customer records, and order amendments in the system.
- Coordinate with customers, factories, warehouses, and logistics providers to ensure timely order fulfilment and shipment. ...
Posted
10 days ago
Customer Service Adviser (12 Months Contract) #JRP Customer Service Adviser (12 Months Contract) #JRP
RECRUIT EXPRESS PTE LTD
SGD2,500 - SGD3,000 Per Month
Central
- Welcome and assist customers in the showroom.
- Understand customer needs and collect customer details for follow-up.
- Maintain showroom appearance and ensure displays are well presented. ...
Posted
10 days ago
Undisclosed
WFH
Singapore
- 5+ years of sales experience
- Proven experience in B2B Sales, particularly in the cloud partner business segment
- Deep industry knowledge involving cloud channel dynamics particularly in cloud distribution and cloud reseller programs across Amazon, Google and Microsoft clouds ...
Posted
10 days ago
Thermo Fisher Scientific
Undisclosed
Singapore
- According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix.
- Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system.
- Ensures allocated tasks are performed on time, within budget and to a high quality standard. Proactively communicates any risks to project leads and line manager as appropriate. ...
Posted
21 days ago
Thermo Fisher Scientific
Undisclosed
Singapore
- Manage all clinical operational and quality aspects of allocated studies, of low to moderate complexity, in compliance with ICH GCP. In accordance to project specific requirements, may assume Clinical Study Manager (CSM) responsibilities on small and/or less complex projects.
- Develop clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan. Contribute to the development of the Master Action Plan (MAP) for providing clinical related documents. Ensure timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central). May participate in the design and development of CRFs, CRF guidelines, patient informed consent templates and other protocol specific documents as required. Collaborate with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meetings.
- Collaborate with the clinical team and other departments as needed to meet deliverables of the project. Regularly communicate with the team and lead team meetings to ensure that timelines, resources, interactions, and quality are maintained. Responsible for the implementation and training of standardized clinical monitoring processes within the study and according to corporate standard policies. Responsible for the timely archiving of documents and study materials for the department. ...
Posted
21 days ago
Thermo Fisher Scientific
Undisclosed
KL City
- According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix.
- Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system.
- Ensures allocated tasks are performed on time, within budget and to a high quality standard. Proactively communicates any risks to project leads and line manager as appropriate. ...
Posted
21 days ago
Thermo Fisher Scientific
Undisclosed
KL City
- Manage all clinical operational and quality aspects of allocated studies, of low to moderate complexity, in compliance with ICH GCP. In accordance to project specific requirements, may assume Clinical Study Manager (CSM) responsibilities on small and/or less complex projects.
- Develop clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan. Contribute to the development of the Master Action Plan (MAP) for providing clinical related documents. Ensure timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central). May participate in the design and development of CRFs, CRF guidelines, patient informed consent templates and other protocol specific documents as required. Collaborate with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meetings.
- Collaborate with the clinical team and other departments as needed to meet deliverables of the project. Regularly communicate with the team and lead team meetings to ensure that timelines, resources, interactions, and quality are maintained. Responsible for the implementation and training of standardized clinical monitoring processes within the study and according to corporate standard policies. Responsible for the timely archiving of documents and study materials for the department. ...
Posted
21 days ago
Thermo Fisher Scientific
Undisclosed
WFH
KL City
- Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings
- resolution. Investigates and follows-up on findings as applicable.
- Participates in investigator meetings as necessary. May help to identify potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Performs trial close out and retrieval of trial materials. ...
Posted
21 days ago
Thermo Fisher Scientific
Undisclosed
Singapore
- According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix.
- Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system.
- Ensures allocated tasks are performed on time, within budget and to a high quality standard. Proactively communicates any risks to project leads and line manager as appropriate. ...
Posted
21 days ago
Thermo Fisher Scientific
Undisclosed
Singapore
- Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings
- resolution. Investigates and follows-up on findings as applicable.
- Participates in investigator meetings as necessary. May help to identify potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Performs trial close out and retrieval of trial materials. ...
Posted
21 days ago
Thermo Fisher Scientific
Undisclosed
KL City
- Manage all clinical operational and quality aspects of allocated studies, of low to moderate complexity, in compliance with ICH GCP. In accordance to project specific requirements, may assume Clinical Study Manager (CSM) responsibilities on small and/or less complex projects.
- Develop clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan. Contribute to the development of the Master Action Plan (MAP) for providing clinical related documents. Ensure timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central). May participate in the design and development of CRFs, CRF guidelines, patient informed consent templates and other protocol specific documents as required. Collaborate with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meetings.
- Collaborate with the clinical team and other departments as needed to meet deliverables of the project. Regularly communicate with the team and lead team meetings to ensure that timelines, resources, interactions, and quality are maintained. Responsible for the implementation and training of standardized clinical monitoring processes within the study and according to corporate standard policies. Responsible for the timely archiving of documents and study materials for the department. ...
Posted
21 days ago
Thermo Fisher Scientific
Undisclosed
KL City
- Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings
- resolution. Investigates and follows-up on findings as applicable.
- Participates in investigator meetings as necessary. May help to identify potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Performs trial close out and retrieval of trial materials. ...
Posted
21 days ago
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