100+ Jsp Jobs - June 2026 - Urgent Hiring
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"jsp"
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Pekerjaan "jsp"
Urus Pemberitahuan
Up to MYR1,600 Sebulan
- Assist with online/marketplace item packing for customers e.g Bright Stor, Pandamart, Grabmart etc.
Jadilah pemohon terawal!
Posted
2 months ago
Up to MYR1,600 Sebulan
- Assist with online/marketplace item packing for customers e.g Bright Stor, Pandamart, Grabmart etc.
Jadilah pemohon terawal!
Posted
2 months ago
SGD3,000 - SGD3,000 Sebulan
Singapore
- Degree or diploma in a relevant field; fresh graduates with strong potential welcome.
- Proficient in Microsoft Office.
- Strong analytical skills and business understanding. ...
Posted
3 days ago
SGD3,200 - SGD3,200 Sebulan
Singapore
- Degree or diploma in a relevant field; fresh graduates with strong potential welcome.
- Proficient in Microsoft Office.
- Strong analytical skills and business understanding. ...
Posted
3 days ago
Undisclosed
- Assist with on-site management to ensure project success
- Ensure project plan is moving forward to meet anticipated deadlines
- Responsible for RFI and submittal process ...
Posted
6 days ago
Undisclosed
KL City
- Vendor Support & Change Enablement: Guide external vendor partners through a brand-new compliance ecosystem, navigating 'unknowns' alongside them and validating their submissions in real time.
- Invoice Auditing: Audit and restructure complex vendor submissions to ensure they map accurately to compliance, and payroll.
- VMS & Data Management: Perform concentrated data entry and employee data management within the Vendor Management System (SAP Fieldglass) to ensure flawless system integrity and data accuracy. ...
Posted
3 days ago
Undisclosed
- :Design end-to-end ISP solutions: broadband, leased line, IP transit, MPLS, SD-WAN, and managed connectivity service
- sTranslate customer requirements into detailed technical architecture, HLD/LLD, and solution documentatio
- nDefine IP network topology, routing design, bandwidth planning, and redundancy strategie ...
Posted
3 days ago
Undisclosed
Singapore
- Responsible for implementing ISP Algorithm into HW using Verilog, SystemVerilog and/or SystemC (High Level Synthesis)
- Verify Logic at ISP level and Digital System level
- Optimize Design for less gate count and low power consumption ...
Posted
2 days ago
SGD5,000 - SGD5,000 Sebulan
Singapore
- Responsible for implementing ISP Algorithm into HW using Verilog, SystemVerilog and/or SystemC (High Level Synthesis)
- Verify Logic at ISP level and Digital System level
- Optimize Design for less gate count and low power consumption ...
Posted
a day ago
SGD150,000 - SGD300,000 Sebulan
Remote
- Ben Edictio Validation & Discussion
- Pre-recorded Interview
- Assessment Test online (Aptitude test)Initial interview ...
Posted
9 days ago
Undisclosed
Singapore
- Perform on-site and remote monitoring visits using a risk-based monitoring approach, including SDV, SDR, and source data review as applicable
- Apply root cause analysis (RCA), critical thinking, and problem-solving skills to identify site issues and implement corrective and preventive actions
- Ensure investigational sites comply with protocol, ICH-GCP, and applicable local regulatory requirements ...
Posted
14 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
3 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
3 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
3 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
3 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
3 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
3 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
3 days ago
Thermo Fisher Scientific
Undisclosed
Kerja di Rumah
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
3 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
3 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
3 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
2 days ago
OMNIVISION TECHNOLOGIES SINGAPORE PTE. LTD.
SGD8,000 - SGD8,000 Sebulan
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
a day ago
Undisclosed
Singapore
- Perform on-site and remote monitoring visits using a risk-based monitoring approach, including SDV, SDR, and source data review as applicable
- Apply root cause analysis (RCA), critical thinking, and problem-solving skills to identify site issues and implement corrective and preventive actions
- Ensure investigational sites comply with protocol, ICH-GCP, and applicable local regulatory requirements ...
Posted
16 days ago
Undisclosed
KL City
- Social-first Ideation & Conceptualization: Drive ‘social-first idea led’ creative solutions that fully utilise addressable channels. Develop and sell innovative social media ideas, content, and activations.
- Content Creation & Execution: Ensure all creative executions meet the highest standard of craftsmanship. While you will work with other creatives, you must be able, when necessary, to create and produce social content/assets independently.
- Scaling & Consistency: Take the lead on scaling social ideas from a lead market across the entire ASP region, ensuring consistency in direction and execution for all social creative output. ...
Posted
6 days ago
Undisclosed
Singapore
- Ensure timely and accurate cargo actualization in the ETRM system while maintaining complete and reliable operational data within trading platforms
- Manage the execution of LNG contracts and charter parties, ensuring full compliance with contractual obligations and agreed terms
- Track key contractual deadlines, milestones, and optionality provisions, working closely with commercial teams to support decision-making ...
Posted
8 days ago
MSI GLOBAL PRIVATE LIMITED
SGD2,410 - SGD2,410 Sebulan
Singapore
- Perform railway operation duties such as safe pedestrian track access control, operate shunting vehicle or passenger/ engineering trains for movement, setting of routes for train movement, etc. in the Test Centre.
- Manage central control at the OCC building to ensure safety and security of the Test Centre operations are compliance with the Safety Manual, Rule Book, etc.
- Co-ordinate with contractors for lifting activities for train delivery into or out of the Test Centre. ...
Posted
9 days ago
Undisclosed
- Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality.
- Leads Local Study Team consisting of CRA(s), CSA(s), for assigned study/studies.
- Leads and optimizes the performance of the Local Study Team(s) at country level ensuring compliance with client Procedural Documents, ICH-GCP and local regulations. ...
Posted
10 days ago
Undisclosed
- Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality.
- Leads Local Study Team consisting of CRA(s), CSA(s), for assigned study/studies.
- Leads and optimizes the performance of the Local Study Team(s) at country level ensuring compliance with client Procedural Documents, ICH-GCP and local regulations. ...
Posted
11 days ago
Undisclosed
Petaling
- Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality.
- Leads Local Study Team consisting of CRA(s), CSA(s), for assigned study/studies.
- Leads and optimizes the performance of the Local Study Team(s) at country level ensuring compliance with client Procedural Documents, ICH-GCP and local regulations. ...
Posted
11 days ago
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Cari Kerja "jsp" Berdasarkan:
Cari Kerja "jsp" Berdasarkan: