553 Csv Jobs - Page 14

Entity :- Accenture Strategy & Consulting Team :- Strategy & Consulting Global Network Practice :- Marketing Analytics Title :- Data Science Manager Job location :- Gurgaon About S&C - Global Network :- Accenture Applied Intelligence practice help our clients grow their business in entirely new ways. Analytics enables our clients to achieve high performance through insights from data - insights that inform better decisions and strengthen customer relationships. From strategy to execution, Accenture works with organizations to develop analytic capabilities - from accessing and reporting on data to predictive modelling - to outperform the competition. WHATS IN IT FOR YOU As part of our Analyti...

Project Role : User Experience Lead Project Role Description : Lead prototype work and other software engineering solutions that create an optimized user experience. Translate design concepts to prototype solutions as quickly and tangibly as possible, with a balanced understanding of technical feasibility implications and design intent. Must have skills : Boomi Atomsphere Integration Good to have skills : NAMinimum 7.5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a User Experience Lead, you will lead prototype work and other software engineering solutions that create an optimized user experience. Your typical day will involve collabor...

Data Transformation: Utilize Data Build Tool (dbt) to transform raw data into curated data models according to business requirements. Implement data transformations and aggregations to support analytical and reporting needs. Orchestration and Automation: Design and implement automated workflows using Google Cloud Composer to orchestrate data pipelines and ensure timely data delivery. Monitor and troubleshoot data pipelines, identifying and resolving issues proactively. Develop and maintain documentation for data pipelines and workflows. GCP Expertise: Leverage GCP services, including BigQuery, Cloud Storage, and Pub/Sub, to build a robust and scalable data platform. Optimize BigQuery perform...

Hands-on experience with ETL testing tools Strong SQL skills Experience with file processing (CSV, XML, JSON) and data validation techniques. Familiarity with scripting languages Knowledge of cloud platforms (AWS, Azure) is a plus.

Handling Following Type of Projects at Site as Leader: PLC System Validation Project - Execution Handle the site engineers as per the project given by Head. Co-ordinate between customers & Head/Senior. prepare the work reports related to project

Experience in operating packing machinery for solid dosage forms Knowledge of GMP, GDP, and safety protocols Attention to detail and documentation accuracy Ability to troubleshoot minor mechanical issues Basic understanding of pharmaceutical regulatory compliance Blister packing Strip packing Bottle filling and labeling lines Preferred candidates who can join on immediately

Job location - Hyderabad Job title - Sr. Network Engineer PC & IS Network engineer Job description - Education and Experience: B.Tech in IT/Electrical Engineering with at least 5 years of experience . Experience working in P&G preferred. Skills Required: Controls & PC&IS: 1. Logic and programming in Allan Bradley PLC 2. Logic and programming in Mitsubishi PLC 3. Communication setup across HDL line PLCs and vision system Network: 1. Defining network architecture (AED/TID) 2. Execution and implementation of network architecture 3. Completing iRisk and CSV for applications 4. Switch and port configuration and enabling firewall rules, configuring ping integrations on applications 5. Establishing...

**Job Summary** The CSV Specialist will lead and support Computer System Validation (CSV) activities, specifically for computerized systems used in the development and manufacture plantswithin a pharmaceutical environment. This role requires a deep understanding of CSV regulations, quality standards, and an ability to ensure compliance with both FDA 21 CFR Part 11, EU Annex 11, and other regulatory requirements. 1. **Validation Planning and Execution** - Lead and manage CSV projects for new and existing computerized systems, ensuring adherence to CSV lifecycle processes and compliance with regulatory standards. - Develop and maintain validation documentation, including validation plans, prot...

Role & responsibilities: Strong experience in catalog management and product data maintenance. Proficiency in tools such as Excel, CSV imports, and catalog management . Familiarity with bulk uploads, product listing, and maintaining product specifications and descriptions. Experience working in a fast-paced, deadline-driven environment.

Dear Candidates, Greetings from KEYBIZ DASHBOARDS, We are looking for Quality Assurance Executive & Sr.Executive injectables&OSD for one of our reputed pharmaceutical client, based at Hyderabad & Vizag location. Please find below openings list. 1.IPQA 2.QMS 3.AQA 4.Validation 5.Equipment Qualification 6.CSV 7.Market Complaints. The above positions we are looking for Hyderabad & Vizag locations, interested please share us updated cv to prasanthi@mydashboards.in or feel free to call on 6305391924 Thanks and Regards Prasanthi - Dashboards Team HR

At Capgemini Invent, we believe difference drives change. As inventive transformation consultants, we blend our strategic, creative and scientific capabilities,collaborating closely with clients to deliver cutting-edge solutions. Join us to drive transformation tailored to our client's challenges of today and tomorrow.Informed and validated by science and data. Superpowered by creativity and design. All underpinned by technology created with purpose. The GxP CSV Validation Engineer ensures that digital systems used in clinical development comply with regulatory standards (GxP, 21 CFR Part 11, EMA Annex 11). They develop and execute validation protocols (IQ, OQ, PQ), risk assessments, and doc...

Role & responsibilities Monitoring Backup jobs training the documentation, and keeping to IT Head approval. Responsible for tracking hardware and software inventory in the ticketing tool. Updating the IT assets Maintaining the labels for all IT assets. Responsible for the Backup Responsible for GMP-related queries and prepared the documentation IT-related bills are filed and kept for approval. PCB-related onsite support and coordinating with vendors supported by the reporting Head. Monitoring and maintaining the CC Cameras infrastructure and escalating to the head if anything is critical. Troubleshooting third-party applications at the Unit level and escalating to the reporting Head to get s...

API -QA

Shift: Night Shift Mandatory skills: 6+ yrs C# Development, .Net Framework, ASP.Net API Responsibilities: - Develop, test, and deploy high-quality C# applications (Console and Web). - Design and manage MS-SQL databases with complex queries and procedures. - Handle data transformations using JSON, XML, and CSV. - Build and maintain ASP.NET Core APIs for internal/external use. - Integrate and consume external APIs. - Conduct code reviews and ensure best practices. - Collaborate with cross-functional remote teams. - Troubleshoot technical issues promptly. - Contribute to process improvements and stay current with tech trends. Qualifications: - 6+ years of C# development experience. - Strong kno...

So, whats the job? You'll lead the design, development, and optimization of scalable, maintainable, and high-performance ETL/ELT pipelines using Informatica IDMC CDI. You'll manage and optimize cloud-based storage environments, including AWS S3 buckets. You'll implement robust data integration solutions that ingest, cleanse, transform, and deliver structured and semi-structured data from diverse sources to downstream systems and data warehouses. You'll support data integration from source systems, ensuring data quality and completeness. You'll automate data loading and transformation processes using tools such as Python, SQL, and orchestration frameworks. You'll contribute to the strategic t...

Responsibilities: Develop, execute, and maintain validation protocols and documentation for PLC/SCADA systems and software. Ensure compliance with relevant regulatory standards, such as 21 CFR Part 11, GAMP 5, and ISO 13485. Conduct risk assessments and identify potential risks associated with PLC/SCADA systems and software. Develop and implement mitigation strategies for identified risks. Work with cross-functional teams to ensure that PLC/SCADA systems and software are designed, developed, and implemented in accordance with validation requirements. Provide technical expertise and support to project teams on validation-related matters. Stay up-to-date on the latest regulatory requirements a...

Werum PAS-X Support Engineer Experience Level: 6-9 Onsite: Bangalore Roles & Responsibilities: System management/Support ITIL, System/Application management experience, CSV knowledge Skill Area: MES Background (Pas-X knowledge preferred) , ITIL, System/Application management experience, CSV knowledge Main Technology: MES/Pas-X Mandatory Skills: (Must Have Skills) Pas-X

Hi, Wishes from GSN!!! Pleasure connecting with you!!! We been into Corporate Search Services for Identifying & Bringing in Stellar Talented Professionals for our reputed IT / Non-IT clients in India. We have been successfully providing results to various potential needs of our clients for the last 20 years. At present, one of our MNC client is hiring Computer System Validation Engineers. PFB the details for your better understanding : 1. WORK LOCATION : CHENNAI 2. Job Role: Engineer / Senior Engineer / Lead 3. EXPERIENCE : 7 to 12 yrs 4. CTC Range: Rs. 15 to 25 LPA 5. Work Type : WFO ****** Looking for SHORT JOINERS ****** Job Description : Min 4+ years of relevant EXP in COMPUTER SYSTEM VA...

We are seeking an experienced professional for the role of Assistant Manager, Computer System Validation (CSV) to join our Risk Advisory team. The ideal candidate will have a strong background in computer system validation within the life sciences and pharmaceutical industry, with a deep understanding of regulatory requirements and validation methodologies. Job Description- Computer System Validation (Assistant Manager) At least 6-7 years of computer system validation experience in a Life sciences and pharmaceutical environment. Good knowledge of cGxP regulations and software lifecycle approaches (e.g., 21 CFR part 11, EU Annex 11, GAMP 5, SDLC Waterfall/Agile methodologies) Having knowledge...

Hi, We are having an opening for R&D-IT Manager-ELN at our Baroda location. Job Summary : R&D-IT Manager will be responsible for the successful implementation of assigned projects. This role requires a strong technical skills and deep compliance understanding of R&D and Lab procedures and processes and the ability to work closely with cross-functional teams to ensure IT applications are running successfully. Experience in ELN implementation is preferred. Role and Responsibilities : ELN implementation for R&D Functions NuGenesis SDMS platform upgrade implementation Implementation of PMS- Store Inventory & Equipment inventory Computer System Validation of scientific software and instrument sof...

Hi, We are having an opening for Executive/Sr. Executive- R&D IT at our Gurgaon location Job Summary : R&D-IT Executive/Sr. Executive will be responsible for supporting IT applications, managing QMS across R&D Gurgaon functions. The person should have a strong understanding of CSV. The role requires a good understanding and experience in R&D/Lab policies and procedures to ensure applications/QMS are comply as per the applicable regulation. Job Description : Role and Responsibilities Application support for R&D applications (PMS, NuGenesis, Empower, Amplexor etc.) Managing and closure of assigned QMS within the timelines Application implementation support, testing and documentation of ongoing...

Role & responsibilities Job Title: Sr. eCompliance Specialist/Manager Education (minimum/desirable): Degree in Life Sciences, Pharmacy, Engineering, or Information Technology; or similar; advanced degree preferred. Languages: Fluency in English (oral and written), additional language(s) a plus. Experience/Professional requirement: 5-10 years of overall experience, and a minimum 5 years of relevant experience in the Pharmaceutical Industry and in particular within regulated functions such as IT Quality and Compliance; CSV compliance. Profound understanding of global regulations and Health Authorities expectations governing computerized systems incl. computerized systems validation, lifecycle ...

Company Description Welcome to AmpleLogic! We're a trusted provider of GAMP solutions, specializing in empowering the life sciences industry through our advanced Application Platform as a Service (aPaaS) platform. We are seeking a highly skilled and detail-oriented Quality Assurance (QA) Specialist with extensive experience in Computer System Validation (CSV) to join our team. This role will focus on ensuring the highest level of compliance, quality, and performance for all software and systems used within our organization, especially those that are regulated under industry standards. The ideal candidate will have a deep understanding of CSV processes, as well as experience working in highly...

locationsIN - Bangalore posted onPosted 10 Days Ago time left to applyEnd DateMay 30, 2025 (13 days left to apply) job requisition idR139071 A.P. Moller - Maersk is an integrated container logistics company and member of the A.P. MollerGroup. Connecting and simplifying trade to help our customers grow and thrive. With a dedicatedteam of over 80,000, operating in 130 countries; we go all the way to enable global trade for a growingworld. From the farm to your refrigerator, or the factory to your wardrobe, A.P. Moller - Maersk isdeveloping solutions that meet customer needs from one end of the supply chain to the other. Team / Opportunity At Maersk, we are transforming to become the global int...

Job Description: Quality Assurance Manager Location: Madhapur, Hyderabad Employment Type: Full-Time Job Summary The Quality Assurance Manager will oversee quality assurance processes for our clinical trial software and AI systems, ensuring compliance with global regulatory requirements, including USFDA (21 CFR Part 11), GDPR, HIPAA, ICH-GCP, ISO 90001 & 27001 and other relevant standards. This role requires deep expertise in Computer System Validation (CSV). With 10+ years of experience, the ideal candidate will lead a QA team, collaborate with cross-functional groups, and drive continuous improvement to deliver reliable, compliant, and innovative solutions. Key Responsibilities of a Quality...