5 Validation Reports Jobs

As a Validation Lead at Livspace, you play a crucial role in offering solutions for both modular and services scope of work to ensure a seamless home interior and renovation experience for our customers. While our dedicated vendors handle modulars, services are delivered through a curated marketplace of Livspace-certified contractor partners and an in-house contracting team. Your responsibilities include: - Validating drawings, Bill of Quantities (BOQ), and site conditions. - Understanding drawings across various disciplines such as modular & non-modular Kitchen, Wardrobe, Storage, furniture, civil, electrical, plumbing, etc., and verifying quantities in the BOQ. - Identifying design discrepancies and anticipating execution risks. - Highlighting any missing line items in the BOQ. - Finalizing the BOQ after resolving design discrepancies and conducting thorough validation at the site. - Providing error-free validation reports within the specified Service Level Agreement (SLA). To excel in this role, you should meet the following job requirements: - Hold a Diploma or B.Tech. in Civil Engineering or Architecture. - Possess at least 3 years of contracting experience, including 1 year in execution and 2 years in Quantity Surveying, preferably in residential or commercial projects. - Demonstrate the ability to assess design feasibility, visualize on-site conditions, and predict execution risks. - Be proactive, capable of prioritizing tasks effectively, and exhibit a high level of ownership. - Have a strong learning aptitude to adapt to evolving project requirements. - Exhibit excellent communication skills, both verbal and written, to effectively interact with stakeholders. Join Livspace, the leading home interiors and renovation platform in Asia, and be part of a dynamic team dedicated to transforming homeowners" dreams into reality. Visit our website for more information: https://www.livspace.com/in/about-us.,

Your main responsibilities as a selected intern will include: Conducting clinical validation tests of ICU ventilators, patient monitors, and other critical care devices in both hospital and laboratory settings. You will collaborate closely with intensivists, respiratory therapists, and ICU staff to evaluate the performance of products. Additionally, you will be responsible for designing and implementing ex-vivo and in-clinic testing protocols to ensure the functionality, accuracy, and safety of devices. You will play a key role in collecting, analyzing, and interpreting clinical data to generate valuable insights for enhancing product improvements. Documenting your findings, preparing validation reports, and contributing to regulatory submissions will be crucial aspects of your role. You will also be expected to identify and troubleshoot any device performance issues and provide constructive feedback to the engineering and Research & Development (R&D) teams for continuous product refinements. Assisting in the development of clinical workflows and best practices for the utilization of Noccarc devices in ICU settings will be an important part of your responsibilities. Moreover, you will be involved in conducting competitor benchmarking studies to ensure that Noccarc's products remain innovative and competitive in the field of respiratory care technology. Your contribution to articles, blogs, and various manuals on best clinical practices, device usage instructions, and journals published by Noccarc will be highly valued. About the Company: Noccarc Robotics is a rapidly growing hardware and med-tech start-up based in India, co-founded by graduates from IIT Kanpur. The company swiftly emerged as a prominent manufacturer of ICU ventilators in India during the early stages of the COVID-19 pandemic in 2020, achieving this feat in less than 90 days. Currently, Noccarc holds a significant market share of 18-20% in the ICU ventilator segment in India. Notably, the company secured its seed funding from the IAN Fund in June 2019 and has been profitable since December 2020, with annual revenues exceeding $11 million. What sets Noccarc apart is its team's proactive approach towards challenges and commitment to delivering effective solutions. The company fosters a result-oriented work culture and boasts a talented young team comprising individuals from prestigious institutions such as IITs, IIMs, NITs, and other renowned colleges. With a workforce of 130 individuals, Noccarc has experienced remarkable growth in revenue over the past two years, establishing itself as a profitable entity in the industry.,

Job Summary: We are seeking a meticulous and detail-oriented NPD (New Product Development) Documentation Specialist to join our dynamic team. The ideal candidate will be responsible for managing and maintaining all documentation related to our NPD process, ensuring accuracy, compliance, and accessibility. This role requires strong organizational skills, a keen eye for detail, and the ability to work collaboratively with cross-functional teams. Responsibilities: Develop and maintain comprehensive documentation for the entire NPD lifecycle, including project plans, design specifications, test protocols, and validation reports. Collaborate with product development, engineering, quality assurance, and regulatory affairs teams to gather necessary information and ensure documentation completeness and accuracy. Ensure all NPD documentation adheres to regulatory requirements and industry standards. Organize and manage documentation in a systematic and accessible manner, utilizing document management systems where applicable. Review and revise documentation as necessary to reflect changes in project scope, schedule, or requirements. Provide training and guidance to team members on documentation standards and best practices. Support audits and inspections by regulatory authorities or external auditors by providing accurate and timely access to documentation. Qualifications: Bachelors degree in a relevant field such as Engineering, Mechanical ,Technical Writing, or a related discipline. Proven experience (5 years) in documentation management within a regulated industry, preferably in new product development or a similar technical environment. Strong understanding of document control practices, quality systems, and regulatory requirements (e.g., FDA, ISO standards). Excellent written and verbal communication skills, with the ability to translate technical information into clear and concise documentation. Proficiency in document management software and tools (e.g., Microsoft Office Suite, SharePoint, Documentum). Highly organized with the ability to manage multiple priorities and deadlines effectively. Attention to detail and a commitment to accuracy in all documentation tasks. Job Type: Full-time Benefits: Flexible schedule Leave encashment Experience: NPD Documentation: 5 years (Preferred) Work Location: In person,

Responsible for Generation of Validation reports & Air Flow Pattern test video all site. Filling vendor registration form. Preparing quotation & sending to Customer after follow up. Preparing Validation Report. Preparing instrument calibration schedule. Scanning and maintaining calibration traceability of instruments in soft and hard copy. Weekly updating validation instrument in stock with co-ordination of validation team. Develop and maintain a QMS compliant with ISO 14644-1,2,3 and related industry standards. Note : Only Female candidates are preferred

Prepare and review validation protocols and reports (IQ/OQ/PQ) in line with GMP/GLP. Coordinate with service engineers for report inputs, data collection, and timelines. Ensure timely and error-free submission of reports to clients. Support the commercial team in responding to client queries related to technical documentation. Maintain accurate documentation for audits and internal quality systems. Coordinate with QA/QC and regulatory departments as needed. Assist in preparing quotations/proposals involving validation/calibration deliverables.