1203 Validation Jobs - Page 7

Description Job Summary This applied technology position creates software that is an integral part of Cummins products. The role involves understanding stakeholder requirements, developing specifications, and taking ownership for the design, implementation, testing, validation, and release of software solutions that control Cummins products across a variety of customer applications. The specialist will also collaborate with OEMs, suppliers, and internal teams to ensure robust system integration and validation. Key Responsibilities Investigate product software issues, analyze causal mechanisms, recommend and implement corrective actions, and document results. Apply and improve product softwar...

Summary As Assoc. Dir. DDIT DEV RA Sol. Del. you will create the detailed IT solution/service design, based on functional specifications to meet quality and performance requirements and technical constraints. Responsible for detailed design, development, and delivery of system solutions for Regulatory Affairs (RA). You will engage with global business leaders and leverage the appropriate IT teams and Functions to determine requirements and deliver data-driven recommendations to improve efficiency and add value. About The Role Position Title: Assoc. Dir. DDIT DEV RA Sol. Arch. Location Hyd-India Hybrid About The Role This role purpose is to act as a consultant and advisor providing guidance t...

Hello All.! We are hiring for the following role. Position: Tech Lead Conga CPQ/CLM & ERP Experience: 79 Years Location: Remote Key Requirements: 35 years of hands-on experience supporting and enhancing Conga CPQ/CLM and ERP systems . Expertise in Conga CPQ/CLM ; serve as the Subject Matter Expert (SME) for CPQ & ERP solutions. Strong in product modeling, pricing configurations, and quote management . Perform system testing, validation , and coordinate with business teams for UAT . Collaborate with cross-functional teams to gather, analyze, and document business requirements . Skilled in creating user stories, defining acceptance criteria , and working in Agile processes . Apply at: [HIDDEN ...

As an Additional Quality Control Analyst at Karuup Pharma, your role will involve the following responsibilities: - Quality specification, inspection, and assessment of raw materials, in process and finished goods including packing material - Clear documentation of lab analysis performed during quality control - Regular supervision of the manufacturing unit hygiene and utilities - Development and research of new product formulations - Timely maintenance of records for stability studies Qualifications required for this position include: - Education: B.Pharm/M.Pharm/Msc Chemistry - Experience: 1-5 years - Key skills: Knowledge in formulations, validation and calibration of QC lab equipment, Ms...

Role Overview: You will be joining the Data Operations group within BSI at Novartis, which is actively contributing to the company-wide digital transformation by leveraging untapped data resources to drive actionable insights. As a Data Engineer, your primary responsibilities will include designing, implementing, and optimizing scalable data pipelines, ensuring data quality, and building robust data infrastructure. Collaboration with various stakeholders and domain experts will be essential to ensure efficient data flow across the organization. Key Responsibilities: - Design, implement, and maintain scalable ETL pipelines to extract, transform, and load data from diverse sources into data wa...

As a Tester I - Semiconductor Product Validation at UST, your role involves assisting in day-to-day operations in Validation and Automation. This includes conducting test case execution on Hardware boards, raising Defects in the tool and performing First level triaging, contributing to team meetings, and sharing innovative ideas. You will also work closely with senior-team members to learn and develop necessary technical skills. Key Responsibilities: - Assisting day-to-day operations in Validation and Automation. - Conducting test case execution on Hardware boards. - Raising Defects in the tool and performing First level triaging. - Contributing to team meetings and sharing innovative ideas....

As a Central Team Change Management Engineer at Micron Technology, your primary role is to provide system setup and configuration changes for MES and BOP/BOI systems used in Backend Manufacturing areas. You will be responsible for supporting change management activities for new Manufacturing systems implementation across the network, collaborating with Central and Site teams across process, equipment engineering, and Manufacturing teams. Additionally, you will be involved in supporting system configuration for Backend Automation Program and its sustainment. This position requires proficiency in project participation, team collaboration, knowledge sharing, and working autonomously. Your key r...

As an Accountant, you will be responsible for various accounting tasks and support functions. Your key responsibilities will include: - Basic accounting entries and reconciliations - Month-end and year-end closing support (prepaid expenses, provisions, accruals, depreciation) - Fixed Assets tracking and capitalization - Data entry and validation in SAP B1 - Preparation of supporting schedules for P&L and Balance Sheet - Assistance in statutory and internal audits - Support in compliance documentation (RBI, ROC, SEZ, etc.) - Coordination for indirect tax filings of foreign subsidiaries - MIS data compilation and reporting - Assistance in budgeting and cost tracking - SAP implementation and au...

Role Overview: At Elanco, you will be the Manufacturing Science & Technology (MS&T) Manager for API, playing a crucial role in ensuring reliable, compliant, and cost-effective API manufacturing. You will collaborate with various departments to support established products, drive process improvements, and facilitate regulatory submissions. Your expertise will be instrumental in enhancing animal health and advancing the company's mission of Food and Companionship Enriching Life. Key Responsibilities: - Serve as the primary technical resource for assigned API manufacturing processes, offering on-site support as required. - Lead technology transfer, process implementation, validation, and improv...

Pharma manufacturing, Quality Assurance, Quality Control, GMP, GLP, HPLC, SOP, Validation, Regulatory Documentation, Production Supervision. For further information, please call -7026629008 / 8050011327

Job Title: New Product Development Trainer Location: Remote Job type: Part -time Job Summary: We are seeking an experienced NPD Trainer with over a decade of hands-on expertise in medical device design, product development, validation, and regulatory compliance . The Trainer will be responsible for designing and delivering structured training programs to upskill engineers, technicians, and project managers in end-to-end new product development processes from concept to commercialization. The ideal candidate should possess strong technical depth, familiarity with ISO 13485, FDA 21 CFR Part 820, and Design Control requirements, and the ability to translate complex product development concepts ...

Location Coimbatore - Tamil Nadu, India Pacesetting. Passionate. Together. HELLA is a listed, internationally positioned automotive supplier operating under the umbrella brand FORVIA. Within this de facto group, HELLA stands for high-performance lighting technology and automotive electronics. At the same time, the Company covers a broad service and product portfolio for the spare parts and workshop business as well as for manufacturers of special-purpose vehicles with its Lifecycle Solutions business group. HELLA has around 36,000 employees at more than 125 locations worldwide and generated consolidated sales of 6.3 billion in the fiscal year 2021/2022. YOUR TASKS Job Objective In the busine...

Opening in Medicamen Biotech Ltd(EU, TGA & ANVISA), Bhiwadi, Raj. Pharma formulation exp. Preferred Qualification: B.Sc./B.Pharma Vacant Post: 10 Nos. QA - IPQA/Docs/Validation QC - IPQC/HPLC/Chemical Testing/GC/KF Mail-ID: hrd@medicamen.com Required Candidate profile Immediate joiner prefer Experience : 2 to 8 Years Ready to Relocate Bhiwadi Self Motivated/ Team Player/ Committed for Performance. E-Mail: hr-ho@medicamen.com Mob: +91 7240001632/ 9992395009

Job Description: Require experience in IPQA, IPQA (API), Qualification (API), Validation (API), Analytical QA, APQR, Stability Studies, regulatory affairs, OOS investigation, Risk Assessment, Market Complaint, QA Documentation, Exposure in QMS, Deviation, CAPA etc with Trackwise system. Qualification - B.Sc./M.Sc./ B.Pharma/ M.Pharma. Experience - 04 to 09 Years. Role & responsibilities Preferred candidate profile The candidate from API background Only to apply. Send CV with Sub : Forwarding CV for position of QA dept to jagpal.dewal@ipca.com

As a Firmware Engineer for power management integrated circuits (PMICs) and systems, your role involves designing and implementing firmware solutions. Collaborating closely with hardware engineers, you will define power management requirements and specifications. Developing algorithms for power state management, sleep modes, and dynamic voltage/frequency scaling are key aspects of your responsibilities. - Optimize firmware for performance, efficiency, and responsiveness to power events. - Conduct testing and validation of power management features, including power profiling and analysis. - Debug and troubleshoot power-related issues in firmware and hardware interactions. - Document firmware ...

As a Firmware Engineer specializing in STM32 with Display at VONI SMARTIoT Pvt Ltd, you will be responsible for designing, developing, and optimizing firmware for STM32 microcontrollers with display interfaces. Your role will involve collaborating with a diverse team to create efficient firmware that drives displays and interacts with various sensors and peripherals. - **Firmware Development:** Develop and maintain firmware for STM32 microcontrollers, focusing on display integration and user interface interaction. - **Display Integration:** Interface with different display technologies like TFT LCDs, OLEDs, or e-paper displays to ensure seamless communication and optimal performance. - **Sen...

Role Overview: As a Manager at PwC, you will be responsible for leading and managing AI and data science projects from design to deployment. Your main focus will be on ensuring high-quality and scalable delivery, translating complex business problems into AI-driven solutions, and architecting AI pipelines and data workflows. You will guide project teams on data engineering, model development, validation, and operationalization. Additionally, you will communicate technical solutions effectively to business stakeholders, foster strong client relationships, and align AI solutions with business goals. Mentoring junior team members and promoting a culture of innovation, learning, and collaboratio...

Role Overview: You will be responsible for preparing and reviewing analytical method transfer/validation/verification protocols and reports. Additionally, you will prepare and review specifications/methods of analysis for various materials and testing processes. You will also be involved in preparing and reviewing justification reports for reducing tests in different testing phases. Monitoring compliance with USP revisions and managing change control for documents will be part of your responsibilities. Moreover, you will prepare and review various reports such as stability time point reduction, enhanced reduced testing, stability summary, and SOPs. Key Responsibilities: - Prepare and review ...

As a Specialist in the Site MS&T team within the Large Molecules Platform at Novartis Healthcare Private Limited in Hyderabad, India, you will work closely with multifunctional technical operations teams. Your role involves executing and supporting Technical Transfers and Life Cycle Management activities, with a strong emphasis on preparing and updating Risk assessments and Validation related documentation. Key Responsibilities: - Utilize Validation and Life Cycle Management Expertise to prepare process and cleaning validation documentation, conduct change evaluations, and ensure compliance with cGMP requirements - Support process validation lifecycle activities and participate in pre-valida...

As a Validation Test Engineer at Capgemini, you will be responsible for performing Flash and protocol conformance validation of control units. Your role will involve preparing test bench setups for ECUs and conducting diagnostics testing. You will be expected to develop test strategies, test plans, and execute tests, as well as analyze test defects and prepare reports accordingly. Additionally, you will be involved in automation tool scripting, verification, and validation. - Develop test strategies, test plans, and execute tests - Analyze test defects and prepare reports - Prepare test bench setups for ECUs - Conduct diagnostics testing - Perform Flash and protocol conformance validation of...

The Systems Engineer V&V (Medical Device) will collaborate closely with cross-functional engineering teams and focuses on supporting the execution of test cases and test strategies, ensuring the high performance and reliability of products in Surgical Robotics. Experience: 4-12 Years Location: Hyderabad (Work From Office) - Hybrid Responsibilities may include the following and other duties may be assigned Work in a multi-disciplinary team developing test methods for a complex, electro-mechanical system Test Method Development, Root Cause Analysis, Capability studies, Fixture Qualification, Risk Management & Non-Product software validation Validate HW/SW Fixtures and Test Methods Write valida...

About Atomgrid Atomgrid is on a mission to revolutionize the global specialty chemicals industry. We are creating a new-age, asset-light, R&D-driven brand that combines pioneering process innovation, market intelligence, and reliable contract manufacturing. We operate across sectors like Agrochemicals, Surfactants & Emulsifiers, Flavours & Fragrances, and Pharmaceuticals. Our growing team of scientists, technology engineers, and project managers is committed to delivering world-class solutions - on time, at the right price, and with unmatched quality. We are founded by IIT & IIM alumni and backed by marquee VCs in India. Read more here. - https://entrackr.com/2024/05/atomgrid-raises-rs-10-cr...

About Atomgrid Atomgrid is on a mission to revolutionize the global specialty chemicals industry. We are creating a new-age, asset-light, R&D-driven brand that combines pioneering process innovation, market intelligence, and reliable contract manufacturing. We operate across sectors like Agrochemicals, Surfactants & Emulsifiers, Flavours & Fragrances, and Pharmaceuticals. Our growing team of scientists, technology engineers, and project managers is committed to delivering world-class solutions - on time, at the right price, and with unmatched quality. We are founded by IIT & IIM alumni and backed by marquee VCs in India. Read more here - https://entrackr.com/2024/05/atomgrid-raises-rs-10-cr-...

Role & responsibilities 1. Preparation and reviewing of CTD and ACTD dossier. 2. Co-ordination with Plant and R&D to collect inputs required for Regulatory Submission. 3. Co-ordination with plant for Regulatory compliances. 4. Timely achievement of monthly plan & timely query response. 5. Gap Analysis/Updation of Master data. 6. Review of Change Controls, Stability Protocol, Clinical Trial Protocols & Artworks. 7. Get feedback from all the countries for respective variation, and there timely submission. 8. renewals. 9. Master data Updating. 10. Follow ups with plant for documentation regularly and review meeting. Tracking and reviewing of document requirements of upcoming new filing in ROW a...

Role Overview: As a Refrigeration Cycle Development Engineer, your main responsibility will be to study global PV in order to create refrigeration cycle variants that meet performance standards and requirements for different regions, all while considering cost targets. Key Responsibilities: - Develop VRF cycles and collaborate closely with other teams to design, validate, and verify cycles. - Lead a team to deliver all technical documents related to cycle design. - Establish and update VRF cycle standards. - Participate in VRF product cost reduction, maintenance, and improvement activities. - Troubleshoot customer complaints and benchmarking activities. In addition to the above, you will als...