1160 Quality Documentation Jobs - Page 2

*Head Q.A. Salary- 8-10 Lac PAExp. 15 years, Good working exposure in process, PDI, Multiple Customer, Customer visit, Customer PPD, QMS and MR activity.Good knowledge of ERP also reqd

The Associate Project Manager (APM) is responsible for managing and delivering consulting projects to Fortune 1000 Customers. He/ She will be owing client engagements and executing these projects parallel till closure. The APM is also responsible for creating project plans, executing those and delivering on time with high quality, value and with customer delight. This is a highly visible and complex role since the candi will be the point of contact and work with executives and users across the entire organization working on multiple accounts. The successful candi must be extremely well organized, focusses on details, process-oriented, quality- minded and has the ability to articulate in writ...

We are seeking motivated and experienced professional who can effectively contribute to the role deliverables connected with position below. In this position you can actively participate to our growth and make a significant impact in a fast-paced environment as: Your contributions to organisations growth: Responsible for QA documents review for receipt parts and coordinating QC activities at receipt. Responsible for project QA activities eg, QAP, Test procedure preparation & approvals, preparing other applicable quality documents and dossier. Conducting testing at various stages eg, DT, NDT, painting, hydro, pneumatic etc Maintain in process assembly checks and quality documents at various l...

Job post summary - CONSULTANCY TO BE DONE AT CLIENT'S FACTORY No requirement to come to office All Trainings Online You can cover manufacturers at any industrial area you prefer Pay: 1,200,000.00 - 2,400,000.00 per year Job description : Senior ISO and ZED Consultant Job Type : Full-time, Permanent, Freelance Remuneration :- 6,00,000 to 12,00,000 per year for ISO , 6,00,000 to 12,00,000 per year for ZED , 18,00,000 for each MCLS cluster of 10 clients for Intermediate and Advance level, which is done in 18 to 24 months. Total Remuneration 12,00,000 to 24,00,000 per year. Hybrid Working Visit to the clients factory is required at your & clients mutual convenience. Schedule: Flexible shift Educ...

Job post summary - CONSULTANCY TO BE DONE AT CLIENT'S FACTORY No requirement to come to office All Trainings Online You can cover manufacturers at any industrial area you prefer Pay: 1,200,000.00 - 2,400,000.00 per year Job description : Senior ISO and ZED Consultant Job Type : Full-time, Permanent, Freelance Remuneration :- 6,00,000 to 12,00,000 per year for ISO , 6,00,000 to 12,00,000 per year for ZED , 18,00,000 for each MCLS cluster of 10 clients for Intermediate and Advance level, which is done in 18 to 24 months. Total Remuneration 12,00,000 to 24,00,000 per year. Hybrid Working Visit to the clients factory is required at your & clients mutual convenience. Schedule: Flexible shift Educ...

Job post summary - CONSULTANCY TO BE DONE AT CLIENT'S FACTORY No requirement to come to office All Trainings Online You can cover manufacturers at any industrial area you prefer Pay: 1,200,000.00 - 2,400,000.00 per year Job description : Senior ISO and ZED Consultant Job Type : Full-time, Permanent, Freelance Remuneration :- 6,00,000 to 12,00,000 per year for ISO , 6,00,000 to 12,00,000 per year for ZED , 18,00,000 for each MCLS cluster of 10 clients for Intermediate and Advance level, which is done in 18 to 24 months. Total Remuneration 12,00,000 to 24,00,000 per year. Hybrid Working Visit to the clients factory is required at your & client’s mutual convenience. Schedule: Flexible shift Edu...

Responsibilities: Conduct regular audits & inspections Ensure compliance with industry standards Develop & implement quality processes Collaborate with cross-functional teams on product improvement Health insurance Annual bonus Provident fund

Essential Criteria: BE/Diploma in electronics Engineering, Knowledge of IATF In-depth knowledge of SMT, Paste printer, AOI, SPI, conformal & X-Ray machine- Programming, Operation & Machine maintenance. Primary Responsibilities : Establishing and maintaining Quality Documentation such as Procedure, Formats, Work and Test Instructions. Calibration management of monitoring and Measuring Instruments from NABL Accredited Laboratories Efficient and Effective planning, organizing, controlling of available resources Coordinating Monitoring and Measuring activities during Inward RM parts QC, In-process QC and Final inspection of FG product. Ensuring that the Corrective and Preventive actions are init...

Develop Inspection Requirement for HV & LV Electrical items based on Tech specification , Standards & Codes Requirements. Independently Conduct Kick-off- meeting & Pre-Fabrication meeting with Domectic and International Supplier. Review supplier quality documents, QAP/ITP, FAT/SAT procedures, technical reports, and compliance documents. Lead and participate in Factory Acceptance Tests (FAT) for electrical equipment such as HV/MV/LV switchgear, transformers,Generators, Varibale Shunt Reactors, UPS systems, battery banks, motors, Cables, MCCs, control panels, and protection systems. Independently conduct shop assessment of domestic and international suppliers. Conduct quality surveillance visi...

- QA/QC role. - Online QA. - Manage Change-overs. - Daily production QA SOP. - Production Monitoring. - Maintain QA/QC parameters. - Conduct the audits. - Manage line clearance. - Manage daily floor operations. Perks and benefits Good Accommodation + Pickup & Drop Facility.

Responsibilities: Lead quality initiatives Ensure compliance with ISO standards Oversee mechanical inspections Develop QC processes for aerospace products Manage QC documentation

ORGANISATIONAL OVERVIEW Lambda Therapeutic Research is a Global full-service Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK) and Warsaw (Poland), we offer comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries. JOB DETAILS 1. Ensure quality documents that objectively and accurately represent the clinical trial data 2. Ensure deliverables are met as per planned and documented guidelines and standard operating procedures 3. Assist with the supervision, plan ...

Qualification : Bachelor s degree in Instrumentation / Mechanical Engineering Experience : 2 5 Yrs Location of Job : Asangaon Key Skills Required: Analytical and problem solving skill Attention to detail Ability to interpret technical drawings and specifications Proficient in the use of quality control tools and software Knowledge of ISO and other relevant quality standards Job Profile : Plan, coordinate, and oversee daily QC activities, including inspections, testing, and audits. Conduct regular inspections of products and materials to identify defects or deviations from specifications. Collaborate with production teams to address and resolve quality issues in a timely manner. Participate i...

Responsible for ensuring all fabricated equipment and components meet technical specifications, codes (ASME, IS, API), and customer standards. Oversees inspection, testing, and documentation from raw material stage to dispatch. Key Responsibilities: Perform stage-wise inspections: fit-up, welding, NDT, hydrotest, final visual Review WPS, PQR, and welder qualifications Coordinate with Third Party Inspectors (TPI) and clients Maintain quality documents: inspection reports, MTCs, DPTMPTUT reports Ensure traceability and conformance to project specifications Monitor and report NCRs (Non Conformance Reports) and assist in CAPA Minimum Qualifications: Diploma B.E. B.Tech Mechanical Engineering Ski...

Purpose/Objective The Incharge Quality (GU) is responsible for developing and implementing a strategic quality control framework for cement production, incorporating Six Sigma and Statistical Process Control (SPC). This role involves overseeing all quality control stages, from raw material analysis to cement dispatch, ensuring adherence to international standards and local regulations. The Incharge Quality (GU)) provides technical guidance on advanced testing methods, drives process optimization and innovation, and manages the QC budget. They enforce health, safety, and environmental compliance, prepare detailed quality reports, and uphold ethical standards in all QC activities. Key Responsi...

Summary The Compliance Manager is responsible for ensuring Kryptons QMS comply with applicable Industry standards and Customer requirements as applicable. The Compliance Manager will be appointed as the Management Representative with the responsibility and authority for oversight of the QMS. Essential Functions Ensure that processes needed for the quality management system are established and implemented. Responsible for creating and maintaining the QMS procedures ensure compliance to regulatory requirements, customer requirements (internal & external) and certifications to International Standards. Report to top management on the performance of the quality management system and note needed i...

Responsible for ensuring all fabricated equipment and components meet technical specifications, codes (ASME, IS, API), and customer standards. Oversees inspection, testing, and documentation from raw material stage to dispatch. Key Responsibilities: Perform stage-wise inspections: fit-up, welding, NDT, hydrotest, final visual Review WPS, PQR, and welder qualifications Coordinate with Third Party Inspectors (TPI) and clients Maintain quality documents: inspection reports, MTCs, DPT/MPT/UT reports Ensure traceability and conformance to project specifications Monitor and report NCRs (Non-Conformance Reports) and assist in CAPA Minimum Qualifications: Diploma / B.E. / B.Tech Mechanical Engineeri...

Responsibilities: * Conduct quality audits & inspections * Ensure compliance with procedures & standards * Develop & implement quality plans * Monitor product/process performance * Prepare final reports & documentation * Preparing ISO Documentation Health insurance Provident fund Office cab/shuttle

Responsibilities: * Lead quality initiatives & improve processes * Ensure compliance with standards & customer requirements * Conduct regular audits & inspections * Manage quality documentation & training programs

Conduct in process and final quality inspections ensuring compliance to customer requirements. Identify defects, anomalies, and areas for improvement through visual examination and testing. Capable of using QC measuring instruments.

Review of analytical data. Preparation of SOPs, Specifications, and method of analysis (Raw material, In-Process and Finished product) Review of DMF to prepare Analytical method and specification Initiate Change Control and Deviation. Good understanding for Impurity profiling Well versed with regulatory agencys current requirement. Well versed with ICH quality guidelines Good knowledge for Pharmacopoeia Good communication especially writing skills for preparing quality documents and coordination with Cross functional teams

Field Coordinator will be responsible for the implementation of field level activities of OFI supported project titled Tackling the root causes of child labour in India spices supply chains in Barmer and Jaisalmer region of Rajasthan. The Field Coordinator will implement planned project activities within the approved budget and timelines with the guidance from the Senior Field Officer and share its up with their supervisor on regular basis. Remain alert and responsive to any child safeguarding risks, acquire relevant knowledge and skills which will enable you to promote strong safeguarding practices, understand the safeguarding policy and procedures and conduct yourself in a manner consisten...

Role & responsibilities Act as Custodian for Clinical protocols at unit level and ensure high standards of patient care Responsible for Interpreting and implementing quality assurance initiatives as per NABH standards in hospital and to ensure delivery of quality care to patients. Development of departmental policies and Procedures, as per NABH norms Ensure compliance to Quality indicator benchmarks and participation in quality initiatives. Undertake focused audits, mocks surveys, surprise audits to assess state of readiness for accreditation and focusing upon continual improvement. Work in association with a consistent team to co-ordinate quality initiatives and provide consistency in such ...

COMPANY PROFILE Shri Bhagwati Machines Pvt. Ltd., (SBMPL), Ajmer (Raj.) is accredited by TUV/SUD ISO, IMS & OH&S 9001: 2015, 14001:2015 & 45001:2018 and Certified OEM. SBMPL was incepted in 1995. We, are pleased to introduce ourselves as a reputed OEM for more than 25 years a leading manufacturer, supplier, and exporter of stone processing machinery at National & International Level. We are always conscious of preparing machines with the latest technology, robust and heavy duty, better performance, productivity and after-sales services. To meet all of the above qualities, SBMPL is the leading manufacturer with an innovative approach to the Mechanical Engineering of Stone Cutters Machines, an...

Hiring for Shanthala Spherocast: Supervise production and quality operations, ensure process control, inspection compliance, documentation, rejection reduction, and smooth coordination with shop floor and management.