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100+ Jsp Jobs - September 2026 - Urgent Hiring
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Tuition Centre Admin SP
MYR5,000 - MYR6,000 Per Month
Fresh Graduates
Petaling, WP Kuala Lumpur
Near Train Station
This company is close to train station
- Greet and assist students, parents, and visitors in a professional and friendly manner, providing information about the tuition centre's programs and services.
- Manage student enrollment, registration, and record-keeping, ensuring all necessary documentation is accurately completed and maintained.
- Handle incoming and outgoing communications, including phone calls, emails, and mail, responding to inquiries and directing them to the appropriate personnel. ...
Posted
3 days ago
Undisclosed
- We are looking for a seasoned Senior Project Manager to take full ownership of OSP/ISP fiber infrastructure projects (FTTx/FTTH). This role acts as the master planner and overall driver of project delivery — responsible for end-to-end planning, execution, client communication, and ensuring projects are delivered on time and within budget. The ideal candidate is a resourceful, hands-on leader with strong troubleshooting instincts and the ability to manage multiple stakeholders simultaneously.
- ## Key Responsibilities
- - Act as overall project owner and master planner, developing detailed project schedules, milestones, and resource plans for OSP/ISP fiber rollouts ...
Posted
16 days ago
Undisclosed
- Free parking
- My jops And nandos worker
- Jana Hana ...
Posted
3 days ago
MYR2,000 - MYR2,000 Per Month
Malaysia
- Bertindak sebagai pemandu JPS untuk pihak pengurusan atasan syarikat.
- Bersedia bekerja di pelbagai lokasi projek, terutamanya di Batu Pahat.
- Boleh dihubungi pada bila-bila masa untuk tugasan segera. ...
Posted
11 days ago
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 process failures and implement corrective/preventive actions to ensure compliance and minimize risks, particularly in complex oncology and CGT studies.
- Ensures data accuracy through SDR, SDV, and CRF review as applicable through on-site and remote monitoring activities.
- Assesses investigational product (IP) handling, storage, and accountability, including considerations for advanced therapies such as cell and gene therapy (e.g., chain of identity/custody where applicable). ...
Posted
3 days ago
Undisclosed
KL City
- Provision, configure, test, and activate enterprise IP and managed network services in collaboration with customers and field engineering teams.
- Perform technical validation of customer service orders to ensure implementation readiness and service quality.
- Support the deployment of services including IPVPN, Ethernet, Metro Ethernet, Cloud, Managed Services, and other enterprise connectivity solutions. ...
Posted
10 days ago
MYR6,000 - MYR8,000 Per Month
- Develop and maintain detailed project schedules using Microsoft Project (MSP).
- Prepare project work programmes, timelines, and activity schedules.
- Monitor project progress against the approved baseline schedule. ...
Posted
10 days ago
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. Identifies 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
12 days ago
NEW HOPE COMMUNITY SERVICES LIMITED
SGD2,580 - SGD2,580 Per Month
Singapore
- Schedule admissions of new residents referred by HDB.
- Attend to and record residents’ enquiries, complaints, or feedback and channel accordingly.
- Contact residents for any matters. ...
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
8 days ago
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. Identifies 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
18 days ago
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 process failures and implement corrective/preventive actions to ensure compliance and minimize risks, particularly in complex oncology and CGT studies.
- Ensures data accuracy through SDR, SDV, and CRF review as applicable through on-site and remote monitoring activities.
- Assesses investigational product (IP) handling, storage, and accountability, including considerations for advanced therapies such as cell and gene therapy (e.g., chain of identity/custody where applicable). ...
Posted
19 days ago
SGD5,500 - SGD6,500 Per Month
Singapore
- Manage a portfolio of corporate clients and provide full spectrum of corporate secretarial services.
- Handle incorporation of companies, preparation of resolutions, AGM/EGM matters and maintenance of statutory records.
- Manage and file ACRA statutory filings, including annual returns, changes in company particulars, directors, shareholders and registered office. ...
Posted
11 days ago
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 process failures and implement corrective/preventive actions to ensure compliance and minimize risks, particularly in complex oncology and CGT studies.
- Ensures data accuracy through SDR, SDV, and CRF review as applicable through on-site and remote monitoring activities.
- Assesses investigational product (IP) handling, storage, and accountability, including considerations for advanced therapies such as cell and gene therapy (e.g., chain of identity/custody where applicable). ...
Posted
19 days ago
Undisclosed
KL City
- Network Provisioning & Service Implementation
- Provision, configure, test, and activate enterprise IP and managed network services in collaboration with customers and field engineering teams.
- Perform technical validation of customer service orders to ensure implementation readiness and service quality. ...
Posted
19 days ago
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
- Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System, CTMS). Performs QC check of reports generated from CTMS system where required.
- Participates in investigator meetings as necessary. Identifies 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. Ensures trial close out and retrieval of trial materials. ...
Posted
12 days ago
Undisclosed
Singapore
- Lead the design, development, and maintenance of the HAL interfaces for peripherals assigned to the HiFi5 DSP. These will likely include peripherals such as timers, PDM interfaces, I2S interfaces, and low-power analog microphone interfaces.
- Evaluate possible RTOS or lightweight schedulers and port these to our SDKs.
- Design and develop boot state machines and IPC/RPC messaging protocols. ...
Posted
13 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
15 days ago
Good News Community Services
SGD2,500 - SGD2,500 Per Month
Singapore
- Prepare financial and management accounting reports for management review and submission to HDB within stipulated timelines.
- Monitor receivables, payables, expenses and cash flow, and follow up on outstanding items.
- Conduct regular bankand account reconciliations and investigate discrepancies. ...
Posted
3 days ago
SGD2,500 - SGD3,500 Per Month
Singapore
- Assist senior engineers with the installation and setup of semiconductor robots and VSP systems at customer sites.
- Support mechanical and electrical installation, equipment setup, alignment, and testing.
- Assist with robot teaching, calibration, parameter setting, and functional checks. ...
Posted
3 days ago
Undisclosed
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
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
7 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
7 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
7 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
7 days ago
Undisclosed
Singapore
- Defining your teamʼs engineering vision, strategy, and directions that align with the organisationʼs overall vision and goals.
- Partnering with stakeholders and cross-functional counterparts (e.g., Product, Design, QA, Security) to prioritise and manage roadmaps, delivering towards product vision incrementally and efficiently.
- Creating and maintaining a long-term technical plan and roadmap for the team; updating it regularly to meet future product/business needs and infrastructure requirements. ...
Posted
9 days ago
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
- Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System, CTMS). Performs QC check of reports generated from CTMS system where required.
- Participates in investigator meetings as necessary. Identifies 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. Ensures trial close out and retrieval of trial materials. ...
Posted
18 days ago
SGD3,000 - SGD3,000 Per Month
Singapore
- Assist in the preparation, review, and execution of contracts and NDAs via Wet-ink or E-Sign.
- Assist to coordinate and schedule interview and meetings.
- Maintain and update procurement records, including contracts, purchase orders, and vendor information. ...
Posted
11 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
11 days ago
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