16 Validation Reports Jobs

As the Head of R&D at Krishang Pharma Private Limited, you will play a crucial role in driving cutting-edge development for regulated markets. You will be responsible for leading end-to-end product development, scale-up, and technology transfer activities. Collaboration with cross-functional teams will be essential to ensure successful product launches, cost-effective processes, and regulatory readiness. Key Responsibilities: - Lead R&D strategy and execution for corticosteroids, hormones, and general APIs - Oversee route scouting, process development, optimization, and plant scale-up - Ensure adherence to GMP, ICH, and international regulatory standards - Coordinate with QA/QC, Regulatory A...

Job Summary: You will be responsible for overseeing and managing the validation processes of systems, processes, or products to ensure compliance with industry standards and regulations. Your role will involve extensive experience in system validation, quality assurance, and compliance management, with a focus on meeting regulatory requirements and ensuring operational efficiency. Key Responsibilities: - Lead and manage system validation activities for projects to ensure compliance with relevant regulatory standards such as FDA, GMP, ISO, and 21 CFR Part 11. - Develop and execute validation plans, protocols (IQ, OQ, PQ), and reports for systems and processes. - Coordinate with cross-function...

As a Sr Engineer-Hardware-Product Engineering at Enphase Energy, you will be responsible for owning the HW Engineering activities of the IQ Battery, which includes Cell pack, BMS, and BiDirectional converter. Your role will involve New Product Design, proposing solutions, Design improvements, Design root cause analysis for mitigating failures, Alternate component qualification, and compliance support. You will collaborate closely with cross-functional teams like FW, Reliability, Quality, Mfg, and Supply Chain to drive solutions into the field. **Key Responsibilities**: - Prime involvement in Product Engineering activities such as New Product Design, Root cause analysis, Design Analysis, reco...

Role Overview: As a Formulations Scientist in Hyderabad, India, you will be responsible for the development of oral solid dosage forms of Non-DEA and DEA substances. Your key functions will include conducting Literature Search, Pre-Formulation, Formulation Design, and Development of stable, Bioequivalent, and Manufacturable generic solid oral formulations. Key Responsibilities: - Act as a mentor and motivator to the team. - Develop robust formulations and processes for immediate release and modified release tablet and capsule dosage forms. - Evaluate patents and develop non-infringement strategies, including the capability of developing Paragraph IV products. - Scale-up and optimize manufact...

Quality Control (QC): Perform analysis of raw materials, intermediates, and finished APIs using HPLC, GC, UV, etc. Maintain analytical data and ensure accuracy as per GMP/GLP. Conduct stability studies and support method validation. Quality Assurance (QA): Review batch manufacturing and analytical records. Ensure compliance with SOPs, GMP guidelines, and regulatory requirements. Handle deviations, change controls, CAPA, and documentation control.

As a Site Transfer and ANDA Specications Specialist at our company, you will play a critical role in creating, revising, and reviewing specifications and methods for site transfers and ANDAs. Your responsibilities will include: - Having knowledge of method validation protocols and being able to create, revise, and review validation reports for drug substance, excipients, and drug products. - Initiating change controls as necessary for various aspects including method and specification revisions, stability protocols, batch analysis, reference standards, characterization of impurities, justification of specifications, facility templates, stability summary reports, 5313 reports, QOS, and stabil...

Executive Market Development (Auto component Filter) - Faridabad Graduate/ Diploma- Mech./Elect. Experience: 3-7 years Age Bracket: 27 to 32 years Interested? Share your CV at shubha@hireindians.com OR Call/WhatsApp: +91 81782 23314 Required Candidate profile Industries Automotive - Filter Industry Responsibilities: Filter market penetration in Faridabad - Ballabgarh & Palwal Samples procurement Fitment & reports Competition monitoring New product testing

Role: Conceptualize and developing of EV powertrain layout and designing components for 2 and 3 Wheelers and their integration. Collaborate with engineering, design, and production teams to ensure seamless integration and timely project delivery. Perform tolerance stack-up analysis for critical drivetrain and electric motor components. Oversee prototype development, testing, and validation processes for EV Powertrain components. Conduct benchmarking and implement performance optimization strategies. Lead the documentation of design specifications, Design releases and testing results for internal reference and potential patent applications. Prerequisites: Good knowledge of Automotive EV power...

The Market Risk and Portfolio Model Validation Specialist position in Mumbai, India, within the Risk division at Deutsche Bank involves managing a wide range of risks including credit, market, and non-financial risks. As part of the Model Risk Management (MoRM) team, you will be responsible for independent model validation and managing model risk globally in alignment with Deutsche Bank's risk appetite. The teams are spread across Mumbai, Frankfurt, Berlin, London, and New York. In this role, you will focus on developing and maintaining a central modelling and validation service for all risk model types and methodologies. You will review and analyze Market Risk and Portfolio models such as V...

We are looking for an innovative and experienced quality analyst to join our team. The quality analyst is responsible for developing and supporting the planning, design, and execution of test plans, test scripts, and process plans for projects. The successful candidate will work closely with various departments to perform and validate test cases based on quality requirements, and recommend changes to predetermined quality guidelines. You will be responsible for ensuring that the end product meets the minimum quality standards, is fully functional and user-friendly. To be successful as a quality analyst, you should demonstrate strong attention to detail and have analytical and problem-solving...

Job Summary: As a Validation Compliance GxP Consultant, you will be responsible for overseeing and managing the validation processes of systems, processes, or products to ensure compliance with industry standards and regulations. You should have extensive experience in system validation, quality assurance, and compliance management, with a focus on meeting regulatory requirements and operational efficiency. Key Responsibilities: You will lead and manage system validation activities for projects to comply with regulatory standards such as FDA, GMP, ISO, and 21 CFR Part 11. Developing and executing validation plans, protocols (IQ, OQ, PQ), and reports for systems and processes is a key part of...

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 discrep...

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 valida...

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 assuranc...

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.