37 Signal Detection Jobs - Page 2

We are looking for a detail-oriented Fresher Pharmacovigilance Associate to join our pharmacovigilance team. In this role, you will assist in monitoring and reporting adverse drug reactions (ADRs), contributing to risk assessment processes, and ensuring compliance with global drug safety regulations. This is an exciting opportunity for someone eager to begin their career in the pharmaceutical industry. Monitor and report adverse drug reactions, assist in risk assessment and ensure compliance with global drug safety regulations. Key Responsibilities: Monitor and collect reports of adverse drug reactions (ADRs) from clinical trials and post-marketing sources. Assist in the preparation and submission of safety reports to regulatory authorities. Support risk assessment activities, including signal detection and data analysis. Ensure compliance with international drug safety regulations and guidelines Assist in maintaining pharmacovigilance databases and documentation. Contribute to safety-related documentation such as periodic safety update reports (PSURs). Support the preparation of audits and inspections related to pharmacovigilance activities.

We are looking for a detail-oriented Fresher Pharmacovigilance Associate to join our pharmacovigilance team. In this role, you will assist in monitoring and reporting adverse drug reactions (ADRs), contributing to risk assessment processes, and ensuring compliance with global drug safety regulations. This is an exciting opportunity for someone eager to begin their career in the pharmaceutical industry. Monitor and report adverse drug reactions, assist in risk assessment and ensure compliance with global drug safety regulations. Key Responsibilities: Monitor and collect reports of adverse drug reactions (ADRs) from clinical trials and post-marketing sources. Assist in the preparation and submission of safety reports to regulatory authorities. Support risk assessment activities, including signal detection and data analysis. Ensure compliance with international drug safety regulations and guidelines Assist in maintaining pharmacovigilance databases and documentation. Contribute to safety-related documentation such as periodic safety update reports (PSURs). Support the preparation of audits and inspections related to pharmacovigilance activities.

We are looking for a detail-oriented Fresher Pharmacovigilance Associate to join our pharmacovigilance team. In this role, you will assist in monitoring and reporting adverse drug reactions (ADRs), contributing to risk assessment processes, and ensuring compliance with global drug safety regulations. This is an exciting opportunity for someone eager to begin their career in the pharmaceutical industry. Monitor and report adverse drug reactions, assist in risk assessment and ensure compliance with global drug safety regulations. Key Responsibilities: Monitor and collect reports of adverse drug reactions (ADRs) from clinical trials and post-marketing sources. Assist in the preparation and submission of safety reports to regulatory authorities. Support risk assessment activities, including signal detection and data analysis. Ensure compliance with international drug safety regulations and guidelines Assist in maintaining pharmacovigilance databases and documentation. Contribute to safety-related documentation such as periodic safety update reports (PSURs). Support the preparation of audits and inspections related to pharmacovigilance activities.

We are looking for a detail-oriented Fresher Pharmacovigilance Associate to join our pharmacovigilance team. In this role, you will assist in monitoring and reporting adverse drug reactions (ADRs), contributing to risk assessment processes, and ensuring compliance with global drug safety regulations. This is an exciting opportunity for someone eager to begin their career in the pharmaceutical industry. Monitor and report adverse drug reactions, assist in risk assessment and ensure compliance with global drug safety regulations. Key Responsibilities: Monitor and collect reports of adverse drug reactions (ADRs) from clinical trials and post-marketing sources. Assist in the preparation and submission of safety reports to regulatory authorities. Support risk assessment activities, including signal detection and data analysis. Ensure compliance with international drug safety regulations and guidelines Assist in maintaining pharmacovigilance databases and documentation. Contribute to safety-related documentation such as periodic safety update reports (PSURs). Support the preparation of audits and inspections related to pharmacovigilance activities.

We are looking for a detail-oriented Fresher Pharmacovigilance Associate to join our pharmacovigilance team. In this role, you will assist in monitoring and reporting adverse drug reactions (ADRs), contributing to risk assessment processes, and ensuring compliance with global drug safety regulations. This is an exciting opportunity for someone eager to begin their career in the pharmaceutical industry. Monitor and report adverse drug reactions, assist in risk assessment and ensure compliance with global drug safety regulations. Key Responsibilities: Monitor and collect reports of adverse drug reactions (ADRs) from clinical trials and post-marketing sources. Assist in the preparation and submission of safety reports to regulatory authorities. Support risk assessment activities, including signal detection and data analysis. Ensure compliance with international drug safety regulations and guidelines Assist in maintaining pharmacovigilance databases and documentation. Contribute to safety-related documentation such as periodic safety update reports (PSURs). Support the preparation of audits and inspections related to pharmacovigilance activities.

We are looking for a detail-oriented Fresher Pharmacovigilance Associate to join our pharmacovigilance team. In this role, you will assist in monitoring and reporting adverse drug reactions (ADRs), contributing to risk assessment processes, and ensuring compliance with global drug safety regulations. This is an exciting opportunity for someone eager to begin their career in the pharmaceutical industry. Monitor and report adverse drug reactions, assist in risk assessment and ensure compliance with global drug safety regulations. Key Responsibilities: Monitor and collect reports of adverse drug reactions (ADRs) from clinical trials and post-marketing sources. Assist in the preparation and submission of safety reports to regulatory authorities. Support risk assessment activities, including signal detection and data analysis. Ensure compliance with international drug safety regulations and guidelines Assist in maintaining pharmacovigilance databases and documentation. Contribute to safety-related documentation such as periodic safety update reports (PSURs). Support the preparation of audits and inspections related to pharmacovigilance activities.

We are looking for a detail-oriented Fresher Pharmacovigilance Associate to join our pharmacovigilance team. In this role, you will assist in monitoring and reporting adverse drug reactions (ADRs), contributing to risk assessment processes, and ensuring compliance with global drug safety regulations. This is an exciting opportunity for someone eager to begin their career in the pharmaceutical industry. Monitor and report adverse drug reactions, assist in risk assessment and ensure compliance with global drug safety regulations. Key Responsibilities: Monitor and collect reports of adverse drug reactions (ADRs) from clinical trials and post-marketing sources. Assist in the preparation and submission of safety reports to regulatory authorities. Support risk assessment activities, including signal detection and data analysis. Ensure compliance with international drug safety regulations and guidelines Assist in maintaining pharmacovigilance databases and documentation. Contribute to safety-related documentation such as periodic safety update reports (PSURs). Support the preparation of audits and inspections related to pharmacovigilance activities.

We are looking for a detail-oriented Fresher Pharmacovigilance Associate to join our pharmacovigilance team. In this role, you will assist in monitoring and reporting adverse drug reactions (ADRs), contributing to risk assessment processes, and ensuring compliance with global drug safety regulations. This is an exciting opportunity for someone eager to begin their career in the pharmaceutical industry. Monitor and report adverse drug reactions, assist in risk assessment and ensure compliance with global drug safety regulations. Key Responsibilities: Monitor and collect reports of adverse drug reactions (ADRs) from clinical trials and post-marketing sources. Assist in the preparation and submission of safety reports to regulatory authorities. Support risk assessment activities, including signal detection and data analysis. Ensure compliance with international drug safety regulations and guidelines Assist in maintaining pharmacovigilance databases and documentation. Contribute to safety-related documentation such as periodic safety update reports (PSURs). Support the preparation of audits and inspections related to pharmacovigilance activities.

We are looking for a detail-oriented Fresher Pharmacovigilance Associate to join our pharmacovigilance team. In this role, you will assist in monitoring and reporting adverse drug reactions (ADRs), contributing to risk assessment processes, and ensuring compliance with global drug safety regulations. This is an exciting opportunity for someone eager to begin their career in the pharmaceutical industry. Monitor and report adverse drug reactions, assist in risk assessment and ensure compliance with global drug safety regulations. Key Responsibilities: Monitor and collect reports of adverse drug reactions (ADRs) from clinical trials and post-marketing sources. Assist in the preparation and submission of safety reports to regulatory authorities. Support risk assessment activities, including signal detection and data analysis. Ensure compliance with international drug safety regulations and guidelines Assist in maintaining pharmacovigilance databases and documentation. Contribute to safety-related documentation such as periodic safety update reports (PSURs). Support the preparation of audits and inspections related to pharmacovigilance activities.

Hi, We are hiring for Leading ITES Company for Aggregate Report Writer Profile. Please Apply, We shall call back relevant profiles. Role & responsibilities: Minimum 2 - 3 years of medical writing work experience including 1 to 2 years of experience in periodic aggregate safety report writing (i.e. PBRER, PSUR, DSUR etc.) To perform all pre-DLP activities and planning for all assigned reports as per client instructions and timelines including the conducting of strategy meeting, kick-off meetings and other ad hoc report related meetings. Performs activities related to the preparation, writing and review of safety portions of Periodic Aggregate Safety Reports (PBRER, DSUR etc.). To perform compilation of all global and country specific periodic aggregate safety reports assigned by the supervisor. To perform peer review of the assigned periodic safety report and complete the corresponding QC checklists within the assigned timeline. To track and drive the progress of safety periodic reports as per the client defined timelines. To ensure compliance to SOPs (client e-manuals and training modules) and other process related documentation. To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : PV Aggregate Mumbai (Job Code # 54) b) For Position in Pune Search : PV Aggregate Pune (Job Code # 55)

Hi, We are hiring for Leading ITES Company for Aggregate Report Writer Profile. Please Apply, We shall call back relevant profiles. Role & responsibilities: Minimum 2 - 3 years of medical writing work experience including 1 to 2 years of experience in periodic aggregate safety report writing (i.e. PBRER, PSUR, DSUR etc.) To perform all pre-DLP activities and planning for all assigned reports as per client instructions and timelines including the conducting of strategy meeting, kick-off meetings and other ad hoc report related meetings. Performs activities related to the preparation, writing and review of safety portions of Periodic Aggregate Safety Reports (PBRER, DSUR etc.). To perform compilation of all global and country specific periodic aggregate safety reports assigned by the supervisor. To perform peer review of the assigned periodic safety report and complete the corresponding QC checklists within the assigned timeline. To track and drive the progress of safety periodic reports as per the client defined timelines. To ensure compliance to SOPs (client e-manuals and training modules) and other process related documentation. To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : PV Aggregate Mumbai (Job Code # 54) b) For Position in Pune Search : PV Aggregate Pune (Job Code # 55)

Role & responsibilities Design & Technical Decision-Making Propose and validate technical electronic design choices , ensuring alignment with system architecture and performance goals. Perform electrical simulations , component stress analyses , and laboratory tests to assess reliability and functionality. Conduct board-level debugging using industry-standard tools (oscilloscopes, logic analyzers, JTAG, signal generators). Verification & Documentation Develop and execute verification procedures based on detailed board requirement specifications. Ensure traceable compliance with upper-level system requirements throughout the design and test phases. Produce high-quality technical documentation , including: Test reports Design definitions Justification files Project Execution & Industrialization Deliver designs within defined cost and schedule constraints , balancing performance with efficiency. Integrate producibility and cost-effectiveness considerations, in collaboration with the industrialization team. Methodology & Regulatory Compliance Apply rigorous engineering methodologies and ensure full compliance with aeronautical standards , including: DO-254 (Design Assurance Guidance for Airborne Electronic Hardware) AMC20 (Acceptable Means of Compliance for airborne systems) Desired Candidate Profile: With a Masters degree in Electronics Engineering , you possess substantial experience in designing analog electronic boards for high-performance and environmentally demanding applications. Your expertise spans: Analog Circuit Design Design of analog systems including: Filters , power supplies , and EMI protection circuits Analog signal conditioning and low-noise sensor interfaces Linear motor control and precision analog feedback loops Independent calculation of key electrical parameters for both simple and complex analog circuits, involving: Transformers , operational amplifiers , MOSFETs , bipolar transistors , diodes , and capacitors ADC/DAC integration and signal conversion optimization. Skilled in laboratory testing , bring-up , and debugging of analog boards using standard equipment: Oscilloscopes Spectrum analyzers Current probes Signal generators Proven ability to build efficient PCB layouts that meet harsh environmental constraints , ensuring mechanical and thermal robustness. Strong awareness of electrical safety standards , consistently applied throughout design, testing, and validation phases.