13 Pil Jobs

Job Description: As a Computer Vision Engineer Developer you will contribute to the development and maintenance of AI pipelines addressing key problems such as object detection item tracking recognition and counting Working under the guidance of senior engineers and data scientists you ll assist in implementing deep learning models preparing datasets and validating performance metrics in real world scenarios This is an ideal role for early career AI professionals who are passionate about CV and eager to grow through exposure to synthetic data foundational models and production grade systems Key Responsibilities: Assist in building and testing CV models for detection tracking classification tasks and latest foundation and VLM models Prepare and annotate image video datasets support data ingestion and cleaning pipelines Contribute to writing and debugging training scripts model loaders and preprocessing functions Run evaluation jobs and generate performance reports using tools like TensorBoard or custom scripts Support error analysis by identifying model weaknesses across edge cases Collaborate with senior engineers on integrating models into scalable inference pipelines Help visualize model outputs draw bounding boxes heatmaps or segmentation masks for explainability Document experiments and code for reproducibility and knowledge sharing Used OpenCV MediaPipe and scikit image for preprocessing motion analysis and visual overlays Integrated DL models with post processing logic e g NMS temporal smoothing event triggering Ensured low latency inference by profiling and tuning frame wise preprocessing Supported integration of RTSP video feeds and video decoders in test pipelines point cloud ingestion and processing Open3D PCL calibration registration ICP FGR 3D detection segmentation with sparse CNNs PointNet and RGB LiDAR IMU fusion Technical Requirements: Good Python skills and working knowledge of PyTorch or TensorFlow Familiarity with image processing libraries e g OpenCV PIL and dataset tools e g COCO format YOLO datasets Eagerness to learn take feedback and contribute in collaborative development environments Exposure to object detection tracking projects academic hackathons or prior work Additional Responsibilities: Basic understanding of synthetic data or 3D asset usage in training pipelines Familiarity with Git Linux command line and Jupyter Notebooks Interest in building a career in computer vision and AI for real world automation Bachelor s degree in Computer Science Data Science or a related technical field 1 3 years of experience or strong internship projects in computer vision or ML model development Preferred Skills: Technology->Artificial Intelligence->Computer Vision,Technology->Artificial Intelligence->Artificial Intelligence - ALL,Technology->Machine Learning->Python

Company Name: Exemed Pharmaceuticals Designation - Drug Regulatory Affairs -Officer/Sr Officer Location - Vadodara ( Corporate Office) Market: Domestic Primary Job Descriptions Having knowledge of SUGAM portal and CDSCO website Submission for Mfg. & Mkt. Applications [CT21/CT-18] for IND, New Drug, Subsequent New Drug, FDC. Application of CT-05 / CT- 04 Application of CT-10 / 12/ 13 Application of import Licenses [CT-16/ Form 12/Form 08] Knowledge of IPC submissions Form 29 application Preparation of presentation for Subject Expert committee (SEC) Product Lifecycle & Management Additionally, should be well verse with Preparation of Module 4 & 5 Nonclinical & Clinical data Preparation of Pack Insert (PI), Patient information leaflet (PIL) and Summary Product Characteristics (SPC) Literature Search (Nonclinical, Clinical, Formulation etc.) Preparation of Product Monograph Preparation of different types of rationales (for FDC, efficacy, dosing etc.) Aware of BABE Guidelines/ CT Phase III guidelines & Animal Toxicology

You will be working as a Python Developer with a focus on Artificial Intelligence and Machine Learning. With 1.5 to 2 years of experience in the field, you will be responsible for tasks such as data mining, data extraction, and utilizing key skills like Python, Big Data, Machine Learning, and Artificial Intelligence. To excel in this role, you should have a basic understanding of statistics, linear algebra, and calculus. A good grasp of data structures is essential, along with proficiency in Python and working knowledge of statistical packages. Your responsibilities will include handling big data sets, performing data extraction, data mining, visualization, and storytelling. You should be comfortable working on both supervised and unsupervised machine learning problems. Experience with specialized packages related to textual data like NLTK and image data like PIL, OpenCV is preferred. Familiarity with deep learning frameworks such as TensorFlow is also beneficial. Hands-on experience in dealing with text and/or image data is required for this role. Knowledge of distributed and parallel processing frameworks like Spark, as well as an understanding of search platforms like Solr/Elastic Search, will be an advantage in successfully fulfilling your responsibilities.,

As a Computer Vision Engineer, you will play a crucial role in transforming business challenges into data-driven machine learning solutions. Your primary responsibility will be to design, develop, and implement computer vision algorithms and models for image and video analysis, object detection, recognition, and tracking. Collaborating with cross-functional teams, you will translate business requirements into technical specifications for computer vision solutions. Staying updated with the latest advancements in computer vision and deep learning, you will identify opportunities for innovation and optimization. To excel in this role, you should have at least 2 years of experience in computer vision and/or deep learning for object detection and tracking, as well as semantic or instance segmentation in academic or industrial domains. Proficiency in Python and related packages such as numpy, scikit-image, PIL, opencv, matplotlib, and seaborn is essential. Additionally, you must possess a strong foundation in data structures and algorithms in Python or C++, along with experience in training models through GPU computing using NVIDIA CUDA or on cloud platforms. Your responsibilities will also include working with large datasets, applying data preprocessing techniques, and optimizing computer vision models for efficiency, accuracy, and real-time performance. Hands-on experience with machine/deep learning frameworks like Tensorflow, Keras, and PyTorch is required, along with expertise in identifying data imbalance, data compatibility, data privacy, data normalization, and data encoding issues. You will be involved in model selection, evaluation, training, validation, and testing, exploring different methods and scenarios for effective outcomes. In this role, you will have the opportunity to work in a dynamic environment with a focus on innovation and collaboration. The position offers a 5-day working week with flexible timings. While we are not currently hiring for the Computer Vision Engineer role, please check back later for potential opportunities to join our team.,

As a Senior Data Scientist / AI Engineer with 8-10 years of experience, you will be a vital part of our team working on developing an AI-enabled ERP solution. Your primary responsibilities will include designing scalable AI models, implementing ML pipelines, and exploring the latest AI technologies to drive innovation. Additionally, you will play a crucial role in managing and mentoring a team of data scientists and AI engineers to foster a collaborative and efficient work environment. Your key responsibilities will involve designing and building AI models from scratch, optimizing machine learning algorithms, and integrating them into our ERP solution. You will also be responsible for developing and maintaining an AI development and deployment pipeline using cloud and containerized solutions. Furthermore, conducting R&D activities to identify opportunities for AI-driven automation, working on sentiment analysis, NLP, and computer vision tasks, and deploying ML models while ensuring seamless integration into production systems will be part of your role. Collaboration with product teams to align AI strategies with business objectives, leading and mentoring a team of data scientists and AI engineers, and fostering a collaborative team culture are essential aspects of this role. Your expertise in Python and ML frameworks, strong understanding of ML algorithms, experience with deep learning architectures, NLP, and computer vision, along with hands-on experience in deploying AI models using Flask APIs, Docker, and Kubernetes are critical for success in this position. Preferred skills include knowledge of Java, experience with software development best practices, understanding of SDLC, version control, CI/CD pipelines, and experience with Big Data technologies. If you are passionate about working with AI-driven products and have a proven track record of solving real-world challenges, we are excited to hear from you! This is a full-time position located in Trivandrum/Kochi, with a remote option available initially. If you have a minimum of 8 years of experience in AI, Machine Learning, or Data Science roles, and have worked on AI model deployment or building AI pipelines, we encourage you to apply. Leadership and team management experience, along with the ability to guide and develop junior team members, are essential requirements for this role. Your strong problem-solving skills, ability to articulate AI concepts effectively, and experience in interacting with clients to communicate AI-driven solutions will be highly valued.,

You will be responsible for running the full production cycle for all Derivatives asset types in AMERS, which includes preproduction and quality analysis, production, and deliveries. Additionally, you will gather requirements for Derivatives products in both vanilla asset types (IRS, Swaptions, FX and Equity Options, CDS, TRS, Inflation swaps) and complex products (Dispersion Swaps, Volatility Swaps, Hybrid products, Exotic Structured Notes). Managing the clients workflow evaluation pricing cycle and supporting TRPS Derivatives clients communications will also be part of your duties. To excel in this role, you should possess a Bachelor's and/or master's degree in Finance, preferably in Quantitative Finance, Mathematical Finance, or Financial Engineering. A well-rounded knowledge of financial markets is essential, along with the ability to independently research and apply complex concepts in a real-world context. You must be self-motivated, have the ability to learn quickly, and operate under tight time constraints. Strong problem-solving skills are crucial, along with proficiency in Excel and good verbal and written communication skills. You should have the confidence and poise to explain and defend evaluations to customers. Preferred skills for this position include experience with Rates using CALYPSO, working with both vanilla and complex derivatives, IRS and Swaptions expertise, familiarity with financial libraries and functions such as PIL, FINCAD, Numerix, and programming experience in scripting languages like C++, JAVA, or Python. As part of the LSEG team, you will be joining a dynamic organization of 25,000 people across 65 countries. Your individuality will be valued, enabling you to bring your true self to work and enrich the diverse workforce. You will experience a collaborative and creative culture that encourages new ideas and is committed to sustainability across the global business. LSEG is dedicated to re-engineering the financial ecosystem to support and drive sustainable economic growth, aiming to achieve growth by accelerating the just transition to net zero, enabling growth of the green economy, and creating inclusive economic opportunity. LSEG offers a range of tailored benefits and support, including healthcare, retirement planning, paid volunteering days, and wellbeing initiatives.,

Role & responsibilities The responsibilities of the role include processing Individual Case Safety Reports (ICSRs) and conducting literature screening activities. The candidate will be responsible for reviewing and assessing the validity of literature abstracts and articles, with further processing into the safety database as required. Additionally, the role involves maintaining the Extended Eudravigilance Medical Product Dictionary (XEVMPD) and performing EVWEB updates, including revisions to the Summary of Product Characteristics (SPC/SmPC) and Patient Information Leaflets (PILs). The candidate will also perform comparative reviews of SmPC and PIL documents against reference products. A key responsibility includes the preparation and maintenance of Risk Management Plans (RMPs), which involve identifying potential risks, outlining mitigation strategies, and ensuring regulatory compliance. Continuous monitoring of safety updates and detection of safety signals for client products is essential. All activities must be conducted in strict compliance with standard operating procedures (SOPs) and applicable regulatory requirements. Preferred candidate profile Eudravigilance, XEVMPD Maintenance, and EVWEB Updates Summary of Product Characteristics (SmPC) and Patient Information Leaflet (PIL) Risk Management Plan (RMP) and Regulatory Documentation ICSR Processing and Reference Product Comparison

Role & responsibilities We are seeking a Pharmacovigilance Associate with 2 to 3 years of experience in the pharmaceutical industry. The ideal candidate should have hands-on experience in processing Individual Case Safety Reports (ICSRs) and performing literature screening to identify safety information. This includes assessing validity of literature abstracts/articles for database entry. The role also involves maintaining XEVMPD, performing EVWEB updates, revising SmPCs, PILs, and preparing Risk Management Plans (RMPs). Monitoring safety updates/signals and ensuring SOP & regulatory compliance is essential. Preferred candidate profile Eudravigilance, XEVMPD Maintenance, EVWEB Updates, SmPC (Summary of Product Characteristics), PIL (Patient Information Leaflet), Regulatory Documentation, Reference Product Comparison, ICSR Process,

Company Name: Exemed Pharmaceuticals Designation - Drug Regulatory Affairs -Officer/Sr Officer Location - Vadodara ( Corporate Office) Market: Domestic Primary Job Descriptions Having knowledge of SUGAM portal and CDSCO website Submission for Mfg. & Mkt. Applications [CT21/CT-18] for IND, New Drug, Subsequent New Drug, FDC. Application of CT-05 / CT- 04 Application of CT-10 / 12/ 13 Application of import Licenses [CT-16/ Form 12/Form 08] Knowledge of IPC submissions Form 29 application Preparation of presentation for Subject Expert committee (SEC) Product Lifecycle & Management Additionally, should be well verse with Preparation of Module 4 & 5 Nonclinical & Clinical data Preparation of Pack Insert (PI), Patient information leaflet (PIL) and Summary Product Characteristics (SPC) Literature Search (Nonclinical, Clinical, Formulation etc.) Preparation of Product Monograph Preparation of different types of rationales (for FDC, efficacy, dosing etc.) Aware of BABE Guidelines/ CT Phase III guidelines & Animal Toxicology

Senior Software Developer (f/m/d) Identifier: INST-SSD-TL Location: Trivandrum For our office in Trivandrum, dSPACE is looking for creative and motivated professionals. You will work on exciting and technologically cutting-edge product development projects, in the areas of control prototyping, code generation and Hardware-In-the-Loop (HIL) simulation. We are currently offering a position as a Senior Software Developer for the development of a product solution that operates within a model-based development environment using MATLAB, Simulink, and Stateflow. As part of the development team, you will be responsible for the development and maintenance of Processor-in-the-Loop (PIL) functionality, which enables the early validation of software components on the processor that will later be used in the ECU. You will also be responsible for developing and maintaining the necessary firmware to integrate new components as part of the PIL functionality. In doing so, you can expect a variety of exciting, challenging, and diverse tasks that you will solve together as a team. Your future colleagues are looking forward to working with you on a wide range of challenging subjects. During the induction period, your colleagues will support you to familiarize you with our products and tasks. Your Tasks You develop and enhance software components within an experienced development team You coordinate new functionalities with stakeholders You analyze microcontroller hardware with the supported compiler to realize the PIL functionality You develop and maintain flash drivers and application interfaces to support PIL Simulation You take ownership of features, independently implement new functionalities, and guide the team in solving complex problems Your Qualifications You have a B.Tech/M.Tech university degree in Computer Science, Electronics and Communication or Electrical and Electronics Engineering, with a minimum of 5 years of relevant experience You are eager to learn and open-minded You have strong proficiency in C and C++, along with experience in Makefile script development You possess deep working knowledge of embedded systems, various microcontroller platforms, and compilers You have strong experience with MATLAB and Simulink You have good experience with testing methodologies for PIL Simulation framework or similar embedded validation environments You are familiar with Azure DevOps and Git for version control and CI/CD workflows You have excellent English communication skills, both written and verbal What We Offer A crucial role in a young, dynamic, and fast-growing team A work environment that fosters trust, respect, and feedback An onboarding buddy to integrate you smoothly into our team Productivity and improvement time between the development sprints A mentor helping you with your personal goals, technical progress in general and your software engineering skills in particular About us dSPACE is a market innovator and leader in providing solutions and systems for embedded controller software development in Automotive, Aerospace and Manufacturing industries. Founded in Germany in 1988, dSPACE employs over 2,600 dedicated people worldwide, who are committed to making the embedded controls software development process more efficient through innovative tools and services. Working at dSPACE means taking on challenging and varied tasks in a promising and exciting industry. With us, you have responsibility and can shape your personal career. A collegial and cooperative approach is as natural for us as the continuous development of your expertise. If you are ready to join our highly successful international team and take on the challenge of creating yet another success story in India send us your application (including motivational letter, CV, copies of your academic degree, references from former employers) at career.tvm@dspace.in indicating your earliest possible entry date.

The task is to develop the Safety concepts for these safety-related system functions for MCUs. Create hazard assessment and risk analysis (HARA). Perform IP, SoC, DFEMA. Develop FuSa Level3 software for MCU. System knowledge ASIL B, C or D system. Required Candidate profile SEOOC(Safety Element Out of Context), FFI (Freedom From Interference) FIT(Failure Intime) Rate Functional Safety Certified – Level 1 / Level 2 / Level 3

Key Responsibilities 1. Dossier Preparation and Submission CTD/eCTD Compilation: Assemble and submit regulatory dossiers in Common Technical Document (CTD) format, including modules for clinical, non-clinical, and quality data.

Role & responsibilities Develop US labeling documents to align with company goals and submission requirements for assigned ANDAs and/or 505(b)(2)s, if required, and ensure labeling meets all legal and regulatory requirements. This includes QC, proofing, editing, and formatting of documents, and coordinating the review and approval of final submission documents. Develop US labeling documents needed for early development projects requiring a human factor or comparative analysis study and ensure established labeling meets all legal and regulatory requirements. This includes QC, proofing, editing, and formatting of documents, and coordinating the review and approval of final submission documents with all relevant departments. Develop labeling content that requires carve-outs due to protected language associated with patents/exclusivities. Serve as a Subject Matter Expert (SME) in all facets of SPL/drug listing, including but not limited to finished product, bulk, and manufacturer under contract. The SME must be able to provide guidance to other team members related to established SPL documents (content and data elements) to ensure alignment with associated applications and applicable FDA regulations and guidance, as well as troubleshoot any validation errors received. Work closely with the SPL Vendor, as well as the FDA Drug Listing team, on any drug listing issues, ensuring a rapid resolution. Prepare and electronically compile full responses to the FDA via the appropriate filing mode. This includes but is not limited to the development of side-by-side comparisons, SPL, and other required submission materials, as necessary. Perform quality reviews of labeling and submission documents by proofreading established files for content accuracy, either manually or by utilizing the electronic proofreading tool TVT. Work closely with external departments, including the CMC and Device teams, to align with internal product/device strategy and processes. Work closely with Regulatory Operations, as well as in Tevas publishing software, to ensure assigned projects are submitted on time following the eCTD requirements related to labeling. Support products falling under Business Development deals, if required, from a labeling/artwork and drug listing perspective. Attend assigned project meetings to ensure labeling timelines are met. Maintain an accurate project tracker of all assigned projects with identified due date priorities and timelines of initial assignment, initiation, and completion of projects. Provide support to the Manager, as needed, in completing the year-end FDA Mandated Blanket No Change certification. This ensures all drug product listings remain active within the agency's National Drug Code (NDC) Directory, preventing potential issues such as disruptions in the market, Medicaid rebates, and other regulatory complications. Assist in the training of new labeling personnel. Maintain knowledge of US regulations, guidelines, and standard operating procedures applicable to US Gx labeling and drug listing. Work in a team environment. Perform all other job-related duties as required by management and dictated by process changes. Preferred candidate profile 7-9 years experience in the Pharmaceutical Industry. Min 6+ years of RA experience will be preferred in the respective Markets. Bachelors in Pharmacy/Master in Pharmacy/Master in science & Life sciences