38 Qms Documentation Jobs - Page 2

Preparing & complying with documents as per QMS/API Q1/EMS/OHS Interaction with certification bodies for audit systems,Training to all concerned in management systems as well as customer specific requirements Customers audits for management systems. Required Candidate profile Candidate should have exeprience in QMS Having experience in Oil/Automotive Industry

As a Senior Manager at Sun Pharmaceutical Industries Ltd located in Halol 1 - Plant, you will be responsible for the operation and maintenance of Utilities such as PW, WFI, Chilled Water, Steam, Compressed Air, and Nitrogen for all blocks. Additionally, you will oversee the operation, maintenance, and distribution of the water system for all blocks to ensure uninterrupted availability of Utilities for processes. Your role will involve conceptualizing and implementing energy conservation measures for both energy and water resources. You will be required to prepare annual revenue budgets, monitor expenses to ensure they are within budget, and propose annual capital budgets for finalization and...

As a QA/QC Engineer at SPECTRON Engineers Private Limited in Mumbai, you will be responsible for developing and implementing QA/QC procedures for both on-site and off-site project execution. Your key responsibilities will include conducting inspections and quality control of electrical, instrumentation, and mechanical works, reviewing WPS, PQR, ITPs, method statements, and third-party test reports, performing material inspection, calibration of instruments, and equipment verification. You will also be coordinating with clients, third-party inspectors, and internal teams for quality audits, ensuring compliance with applicable standards such as IS, API, ISO, and ASTM, as well as project specif...

Role & responsibilities * Moulding Process Management : Set, monitor and optimize moulding parameters for consistent part quality. Trouble-shoot process-related issues to minimize downtime and scrap. * Part Trial & Development : Lead new mould and part trials including validation and sample submissions (PPAP). Collaborate with tool room, QA and design teams for first-time-right trials. Maintain detailed records of part history, parameter settings, and change control. * QMS Documentation Prepare and maintain process-related documents : Process Flow, PFMEA, Work Instructions, Control Plan. Ensure compliance with ISO 9001 / IATF 16949 standards. Support internal/external audits with proper docu...

Role & responsibilities Sr.Executive : QMS & engineering documentation Primary Responsibilities: 1. Responsible for GMP compliance, as per procedures define and implementations of GxP practices. 2. To ensure the GDP and data integrity in routine/daily activities/operations. 3. Responsible for QMS documents related to engineering. 4. Audits & compliance 5. Preparation of SOPs, review & periodic revisions 6. To attend /or supervise all jobs related to Electrical/ Instrumentation Engineering activities at site. 7. Timely execution of equipments/instruments as per schedule coordination with user. 8. To attend emergency breakdowns of all plant wide machines round the clock as and when required. 9...

Ensure the adherence of Supplier Quality and In-coming Quality Maintain Incoming parts quality, supplier monitoring and supplier audit Be Part of CFT to have concrete AOI development with CD team during development. Evaluate supplier product quality on regular basis and guide them to achieve consistency in quality. Participate in supplier CAT Meeting. Preparing and implementing supplier wise annual audit plan to improvement and evaluate the suppliers Analyzing the audit report and action plan from supplier for closing NCs Issue Supplier notification for quality issue, debit etc. Adherence of quality systems at In-process Quality Conduct the Internal audit of product & Manufacturing Processes...

Role & responsibilities To manage Quality management system (QMS) in accordance with the Stellantis Quality Policy & Framework To Roll out the QMS standards and ensure the training and implementation in respective domain To assess the maturity of the QMS in all domains based on existing on-field practices To identify and prioritize audits needs depending on customer risks, regulatory requirements and the QMS maturity and guarantee the outcome of the corrective action plans, To execute yearly Audits comprising the System (IATF 16949 & ISO 9001), Start of Production readiness, Conformity of Production & Specific Audits, including closure of non-conformities. Liason with the external certificat...

Role & responsibilities 01 Quality Control Functions: 1.1 To ensure that the laboratory carrying out its testing, calibration, validation and all other technical activities in such a way to meet GLP requirements. 1.2 To carry out all technical activities and implementation of documented quality system. 1.3 To plan, schedule and monitor analysis of Raw Materials, Premix, Packing Materials, In-process materials, Finished products, Microbiological analysis, Water analysis and ensure that they meet defined relevant quality standards. 1.4 Periodically review logbooks, reports and test protocols related to Raw Materials, Premix, Packing Materials, Microbiological analysis, In-process and Finished ...

Good knowledge of QMS, Change control , Deviation. Having knowledge of Validation, APQR and other qulaity complience. Quality Management System (QMS) Implementation and Maintenance: Assist in the development, implementation, and maintenance of the QMS. Ensure compliance with relevant quality standards (e.g., ISO 9001, GMP). Maintain and upadate QMS documentation, including procedures, work instructions, and forms. Quality Control and Inspections: Conduct inspections and tests of products, processes, and materials. Identify and document non-conformances and deviations. Monitor and analyze quality data to identify trends and areas for improvement. Auditing and Compliance: Conduct internal audi...

1. Responsible for Raw material testing, In process Inspection, Final Inspection & PDI 2. Responsible for Customer Quality and timely calibration of various instruments 3. Candidate have exp in quality inspections, audits,failure analysis, QMS documentation, and team leadership, ensuring adherence to ISO, IATF, CSR to drive operational excellence. 4. Prepare the rejection & Scrap details on Daily/Monthly basis & Do analysis to control the rejection. 5. Handling Customer Complaint & Making 8D (Internal& External) to avoid thecomplaint. 6. Having Knowledge of 7 QC Tools, 5 Core Quality Tools and Maintaining MIS, Defect Analysis, Customer Complaint & find out the root cause & analysis the same ...

The Project Engineer will be responsible for the preparation, review, and management of essential project documentation including User Requirement Specifications (URS), Piping and Instrumentation Diagrams (P&ID), Qualification documents (DO, 1Q, OQ), Gantt charts, and relevant QMS documentation. This role will work closely with the cross-functional teams to ensure alignment with GMP and regulatory standards from the early design phase through to final qualification. In addition to documentation, the role will require hands-on coordination with vendors and contractors for timely execution of site works. This includes floating enquiries, obtaining and reviewing technical and commercial offers,...

Basic Role Details Division/ Department - Quality Assurance / R&D Location - Hardware Park (Hyderabad) This Role Reports to - Sr. General Manager - QA & R&D This Role Supervises - Lab Engineers / Design Engineers Purpose Of The Role To take care of the new product and process Design and Existing product and process Quality improvement Ideal Profile Educational Qualification - Essential: B.E./ B.Tech /M.Sc. with specialization in Electronics/Electrical Engineering, from a State/Govt. recognized University Preferred : Electronics/ Electrical/ Mechanical Work Experience Required (In yrs.) - Total: 5-8 yrs. Years (Relevant experience): 3-5 yrs. Other Relevant Direct Skills - AutoCAD / Relevant d...

Role & responsibilities Strong knowledge of SOP preparation, documentation structure, and revision cycles Experience in handling QMS documentation (e.g., change control, impact assessments, etc.) Good understanding of regulatory requirements Excellent written communication and organizational skills High attention to detail with the ability to manage multiple documentation tasks Hands-on experience with Caliber LIMS Preferred candidate profile The incumbent should have adequate knowledge in QMS documentation, Caliber LIMS & SOP preparation