359 Quality Documentation Jobs - Page 7

Amazon is looking for a data-savvy professional to create, report on, and monitor business and operations metrics. Amazon has a culture of data-driven decision-making, and demands business intelligence that is timely, accurate, and actionable. This role will help scope, influence, and evaluate process improvements, and will contribute to Amazon s success by enabling data-driven decision making that will impact the customer experience. You love working with data, can create clear and effective reports and data visualizations, and can partner with customers to answer key business questions. You will also have the opportunity to display your skills in the following areas: * Own the design, development, and maintenance of ongoing metrics, reports, analyses, dashboards, etc. to drive key business decisions. * Analyze the current testing processes and identify improvement opportunities with define requirements and work with technical teams and managers to integrate into their development schedules. * Demonstrate good judgment in solving problems as well as identifying problems in advance, and proposing solutions. * Derive actionable insights and present recommendations from your analyses to partner teams and organizational leadership. * Translate technical testing results into business-friendly reports * Have a strong desire to dive deep and demonstrate the ability to do it effectively. * Share your expertise partner with and empower product teams to perform their own analyses. * Produce high-quality documentation for processes and analysis results. A day in the life We are looking for a Business Analyst to join our team. This person will be a creative problem solver who cares deeply about what our customers experience, and is a highly analytical, team-oriented individual with excellent communication skills. In this highly visible role, you will provide reporting, analyze data, make sense of the results and be able to explain what it all means to key stakeholders, such as Front Line Managers (FLMs), QA Engineers and Project Managers. You are a self-starter while being a reliable teammate, you are comfortable with ambiguity in a fast-paced and ever-changing environment, you are able to see the big picture while paying meticulous attention to detail, you know what it takes to build trust, you are curious and thrive on learning. You will become a subject matter expert in the Device OS world. About the team The Amazon Devices group delivers delightfully unique Amazon experiences, giving customers instant access to everything, digital or physical. The Device OS team plays a central role in creating these innovative devices at Lab126. The Device OS team is responsible for the board bring up, low level software, core operating system architecture, innovative framework feature development, associated cloud services and end-to-end system functions that brings these devices to life. The software built by the Device OS team runs on all Amazon consumer electronics devices. 3+ years of Excel or Tableau (data manipulation, macros, charts and pivot tables) experience 2+ years of complex Excel VBA macros writing experience Experience defining requirements and using data and metrics to draw business insights Experience with SQL or ETL Experience creating complex SQL queries joining multiple datasets, ETL DW concepts Experience in Amazon Redshift and other AWS technologies

Roles and Responsibilities Develop and implement quality management systems (QMS) policies, procedures, and guidelines to ensure compliance with regulatory requirements. Conduct internal audits to identify areas for improvement and implement corrective actions to address non-conformities. Prepare and maintain accurate records of quality documentation, including standard operating procedures, work instructions, and training materials. Collaborate with cross-functional teams to develop new products or processes that meet customer needs while ensuring adherence to quality standards. Ensure ongoing monitoring of production processes to detect deviations from specifications and take corrective action as needed. Desired Candidate Profile 14-20 years of experience in Quality Assurance & Regulatory Affairs with expertise in QMS implementation. Strong understanding of pharmaceutical regulations such as FDA, GMP, ISO 9001:2015 etc. Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma).

Conduct and lead audits to ensure compliance with ISO 9001 and ISO 45001 standards. Manage team Review and audit the Costruction Quality Find gaps in Method Statements Prepare documents and Reports Do audits with safety complaince

Responsibilities: * Ensure product compliance with quality standards through inspections & audits. * Collaborate with production team on process improvements. * Conduct regular quality control checks using ISO methods. Annual bonus Provident fund

Q.M.S & Quality Assurance Responsible for implementation, monitoring and maintenance of QMS, EMS, OHSAS, IATF in all the units of organization. To Prepare and review the quality management system, environment management system and other system related documents. To report to top management on the performance of the documented quality management system, environment system and other systems as a basis for improvement of the quality system. To ensure that the quality/environment system is established implemented and maintained in accordance with standards. Well aware about 5 core tools like APQP, MSA, PPAP, FMEA and SPC and ensure that all applicable requirements of these standard manuals are implemented. To conduct Process and Product Audit as per the defined checklist and to ensure that it is working as per the Documented Quality System. To ensure that the continual improvement is going on after implementing the system. To liaise with certifying body for all the matters related to QMS/EMS and other standards. To establish control over document and data including documents of external origin. To establish control over records. To schedule and arrange Internal quality audits as per documented procedures. To conduct management review meeting as per defined frequency and as per documented procedure make minutes of meeting and circulate after approval of top management. To arrange system related trainings. To liaise with consultant. To ensure promotion of the customer requirements throughout the organization. To ensure promotion of the customer requirements throughout the organization. To ensure that all the raw materials are issued to production department only after necessary inspection and test are done and released by lab. To ensure that all the inspection, measuring and test equipment used in Quality control department are calibrated before validity for the same gets expired. To make necessary arrangements for customers/third party inspection, if any. To conduct process and product Audit as per the defined as per the documented quality system. Responsible for customer complaint handling, Joint inspection & field return product analysis & actions. Responsible for arranging customers visit/audit at plant. Responsible for BIS inspection & renewal of license.

Responsible for implementation, monitoring and maintenance of QMS, EMS, OHSAS, IATF in all the units of organization. To Prepare and review the quality management system, environment management system and other system related documents. To report to top management on the performance of the documented quality management system, environment system and other systems as a basis for improvement of the quality system. To ensure that the quality/environment system is established implemented and maintained in accordance with standards. Well aware about 5 core tools like APQP, MSA, PPAP, FMEA and SPC and ensure that all applicable requirements of these standard manuals are implemented. To conduct Process and Product Audit as per the defined checklist and to ensure that it is working as per the Documented Quality System. To ensure that the continual improvement is going on after implementing the system. To liaise with certifying body for all the matters related to QMS/EMS and other standards. To schedule and arrange Internal quality audits as per documented procedures. To conduct management review meeting as per defined frequency and as per documented procedure make minutes of meeting and circulate after approval of top management. To arrange system related trainings To liaise with consultant. To ensure that all the raw materials are issued to production department only after necessary inspection and test are done and released by lab. To ensure that all the inspection, measuring and test equipment used in Quality control department are calibrated before validity for the same gets expired. To make necessary arrangements for customers/third party inspection, if any. To conduct process and product Audit as per the defined as per the documented quality system. Responsible for customer complaint handling, Joint inspection & field return product analysis & actions. Responsible for arranging customers visit/audit at plant.

Ensure quality as per IS codes, approve specs/methods, inspect materials, supervise site, manage tests/docs, issue NCRs, audit support, vendor checks & report coordination.

Ensure quality as per IS codes, approve specs/methods, inspect materials, supervise site, manage tests/docs, issue NCRs, audit support, vendor checks & report coordination.

Responsibilities: Handle customer quality complaints Manage and submit PPAP prepare 8D reports Operate and interpret reports from CMM Maintain detailed inspection records and reports for traceability. Provident fund

Quality control engineer required at kundli sonipat Qualification- Any mechanical Exp- min 5 yrs Salary- 25k to 30k skills- Sheetmetal experience required

1. Inspect raw materials, components, and finished products to ensure they meet quality specifications 2. Analyze data, investigate defects, and develop corrective actions 3. Establishing standards, procedures, and documentation

OPENTEXT - THE INFORMATION COMPANY OpenText is a global leader in information management, where innovation, creativity, and collaboration are the key components of our corporate culture. As a member of our team, you will have the opportunity to partner with the most highly regarded companies in the world, tackle complex issues, and contribute to projects that shape the future of digital transformation. AI-First. Future-Driven. Human-Centered. At OpenText, AI is at the heart of everything we do powering innovation, transforming work, and empowering digital knowledge workers. Were hiring talent that AI cant replace to help us shape the future of information management. Join us. Your Impact We are seeking a skilled and motivated Technical Writer to join our team. We are an enterprise software product company with technical and domain specific offerings. As an individual contributor, you will play a crucial role in creating high-quality technical documentation and content to support our products. In our hybrid work mode, everyone works from office three days a week. This setup offers the perfect balance between collaboration and flexibility, ensuring effective communication and coordination within the team. What The Role Offers If you are passionate about technical writing and thrive in a dynamic, agile, and collaborative environment, we invite you to join our team as an individual contributor in this pure technical writing role. What you will need to succeed 3+ years of experience in technical writing. Degree in any discipline, preferably, information science or computer applications. Native-level proficiency in English with exceptional grammar skills. Instructional proficiency in software-related concepts and terminologies. Technically savvy and enjoys learning and explaining technical concepts. Professional working proficiency in MSTP (Microsoft Manual of Style for Technical Publications). Professional working proficiency in technical writing best practices. For example, organizing content, chunking, minimalism, re-use, etc. Individual contributor responsible for creating and maintaining end user documentation. Work with scrum teams and SMEs to create and validate documentation. Passion for research You enjoy conducting in-depth research to gather the necessary information for creating accurate and comprehensive technical documentation. Collaborative mindset You thrive in collaborative environments, actively seeking input and feedback from subject matter experts and cross-functional teams to ensure the highest quality documentation. Team player You are a valuable team player, capable of effectively collaborating with colleagues to achieve shared goals and objectives. Self-motivated You possess a strong internal drive and motivation, allowing you to work independently, meet deadlines, and consistently deliver high-quality results. Results-oriented You have a proven track record of delivering outcomes and achieving tangible results, demonstrating a results-oriented approach in your work. Passion for explanation You enjoy explaining complex technical concepts in a clear and understandable manner, ensuring that end-users can easily grasp the information provided. Dedication to simplification You are committed to simplifying complex ideas and processes, transforming them into user-friendly and accessible documentation. One Last Thing OpenTexts efforts to build an inclusive work environment go beyond simply complying with applicable laws. . Our proactive approach fosters collaboration, innovation, and personal growth, enriching OpenTexts vibrant workplace.

QC Engineer skilled in inspection, NDT, and quality standards (ASTM, ASME, JIS, EN). Expert in reading drawings, using measuring tools, and preparing QA/QC documents. Handles in-process/final checks, testing, NCRs, and audits.

Job Summary: ON-SITE ROLE The Production Associate Level I is responsible for the safe and efficient operation of machines and production equipment within a manufacturing environment. Working under direct guidance, this role ensures compliance with quality standards, production targets, and safety protocols while supporting team-based initiatives and continuous improvement. Key Responsibilities: 1. Health, Safety & Environmental (HSE): Immediately stop work and report any major injury hazards. Report all work-related injuries, illnesses, incidents, or hazards. Comply with all HSE standards, regulations, and procedures. Wear and maintain proper personal protective equipment (PPE). Promote interdependent safety by supporting co-workers' well-being. Correct hazards within your scope and capabilities. Understand environmental impacts of tasks and work to reduce them. Participate in mandatory HSE training activities. 2. Quality: Follow all applicable standard work procedures and quality documentation. Perform quality inspections and report issues promptly. Identify and contain non-conforming materials. Raise concerns to prevent quality and cost issues. 3. Delivery & Operations: Operate manual and automated machinery to produce or assemble products to specification. Meet production goals and maintain pace with required cycle times or engineering standards. Maintain a clean and orderly workspace, including housekeeping and machine care. Perform routine operator maintenance and equipment checks. Collaborate with maintenance and technical staff to report equipment issues. Remain flexible to perform other duties as needed to meet production demands. 4. Teamwork and Continuous Improvement: Communicate effectively with team members and support staff. Participate in required training and personal development activities. Actively engage in initiatives to improve safety, quality, workflow, and team performance. External Qualifications and Competencies Core Competencies: Collaborates: Builds strong partnerships and works cooperatively with others. Communicates Effectively: Shares information clearly and appropriately for different audiences. Customer Focus: Understands customer needs and delivers relevant solutions. Demonstrates Self-Awareness: Seeks feedback and uses it to grow. Nimble Learning: Quickly learns from both successes and failures. Self-Development: Takes initiative for personal and professional growth. Health and Safety Fundamentals: Proactively promotes a safe and injury-free workplace. Values Differences: Embraces diverse perspectives and fosters inclusion. Qualifications: Education, Licenses, Certifications: Diploma in Mechanical/ Automobile/ Production. May require licensing for compliance with export control or trade sanction regulations. Experience: Min. 2 years of experience in Assembly required. Internal candidates must demonstrate the ability to safely and effectively operate production equipment with direct guidance. Additional Responsibilities Unique to this Position Skills and Attributes: Diploma with 2+ years experience in Production profile. Basic mechanical aptitude and understanding of manufacturing processes. Ability to follow instructions, procedures, and safety protocols. Attention to detail and a commitment to quality. Team-oriented mindset with good communication skills. Willingness to learn and adapt in a fast-paced production environment.

Responsibilities: Develop & implement quality procedures. Conduct regular audits & inspections. Ensure compliance with industry standards Maintain accurate documentation. Client co ordination and follow quality standards of client Health insurance Provident fund

Manage the Quality Assurance function at manufacturing site Ensure compliance with ISO, GMP & REACH standard Develop, implement & monitor Quality Management Systems including SOPs, documentation & CAPA systems Handle customer complaints, conduct RCA Required Candidate profile 8–12 years of experience in QA, preferably in specialty chemicals Knowledge of analytical instruments, QC processes & technical documentation Strong knowledge - ISO 9001, GMP & other quality standards

Summary To write, review and/or manage the production of high quality clinical and safety documentation for submission to regulatory authorities in support of marketing applications. To provide documentation related consultancy to other line functions. About the Role Major accountabilities: To author and review high quality clinical and safety documents: non-registration Clinical Study Reports (CSR), Development Safety Update Reports (DSUR), Risk Management Plans (RMP). 2. Lead for outsourced Narrative projects. Coordinate other outsourced activities in RWS. 3. Core member of Clinical Trial Team (CTT) / participate in Safety Management Team (SMT). 4. Actively participate in planning of data analyses and presentation used in CSRs. 5. Act as documentation consultant in CTTs and SMTs to ensure compliance of documentation to internal company standards and external regulatory guidelines. 6. May act as Program Writer ensuring adequate medical writing resources are available for assigned program and consistency between documents. 7. Act as liaison between CTTs and publishing teams to ensure timely delivery of final documents for publishing. 8. Support the development of RWS through participating in RWS workstreams and other related activities. 9. Contribute to development of processes within RWS. May contribute to cross-functional initiatives. 10. Fostering cross-functional communication to optimize feedback and input towards high quality documents. 11. Maintain audit, SOP and training compliance. Key performance indicators: Delivery of high quality clinical and safety documents in time and in compliance with internal and external standards -Customer / partner/ project feedback and satisfaction -Adherence to Novartis policy and guidelines Minimum Requirements: Work Experience: Minimum 3-5 years of medical writing experience or 1-3 years of experience with MBBS/PhD. Good knowledge of and some experience in global regulatory environment and process (key regulatory bodies, key documents, approval processes, safety reporting requirements). Knowledge of process for and some experience in global registering of drugs (simple submissions). Excellent communication skills (written, verbal, presentations) Very good understanding of biostatistics principles. Ability to prioritize and manage multiple demands and projects. Ability to define and solve complex problems ( Problemsolver ) Broad knowledge and future oriented perspective Proven track record in matrix environment Experience in contributing to global, cross-functional projects. Global, cross-cultural perspective and customer orientation Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients lives. Ready to create a brighter future together? https://www. novartis. com / about / strategy / people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork. novartis. com/network Benefits and Rewards: Read our handbook to learn about all the ways we ll help you thrive personally and professionally:

Testing of all Dairy product Follow by SOPs Manual Ex. Milk quality, Ghee, Butter, Curd, G.J. Mix Powder, Colostrum Powder, Milk Powder (SMP, WMP), Whey Powder (DM-40, DM-70, WPP, WPC- 35, WPC-80, WPI-90) & its record as well as result.

Std room operations and experience of -CMM , Contour , Profile projector , Surface roughness measurement , Calibration of instruments GD&T Quality system IATF 16949 requirements .Exposure to various customer audits TPM QM Pillar activities. Required Candidate profile 8 -12 YEARS working experience, DME, Std room operations and Hands on experience of -CMM, Quality System,IATF 16949 documents etc

OPENTEXT - THE INFORMATION COMPANY OpenText is a global leader in information management, where innovation, creativity, and collaboration are the key components of our corporate culture. As a member of our team, you will have the opportunity to partner with the most highly regarded companies in the world, tackle complex issues, and contribute to projects that shape the future of digital transformation. AI-First. Future-Driven. Human-Centered. At OpenText, AI is at the heart of everything we do powering innovation, transforming work, and empowering digital knowledge workers. Were hiring talent that AI cant replace to help us shape the future of information management. Join us. Your Impact We are seeking a skilled and motivated Technical Writer to join our team. We are an enterprise software product company with technical and domain specific offerings. As an individual contributor, you will play a crucial role in creating high-quality technical documentation and content to support our products. In our hybrid work mode, everyone works from office three days a week. This setup offers the perfect balance between collaboration and flexibility, ensuring effective communication and coordination within the team. What The Role Offers If you are passionate about technical writing and thrive in a dynamic, agile, and collaborative environment, we invite you to join our team as an individual contributor in this pure technical writing role. What you will need to succeed 3+ years of experience in technical writing. Degree in any discipline, preferably, information science or computer applications. Native-level proficiency in English with exceptional grammar skills. Instructional proficiency in software-related concepts and terminologies. Technically savvy and enjoys learning and explaining technical concepts. Professional working proficiency in MSTP (Microsoft Manual of Style for Technical Publications). Professional working proficiency in technical writing best practices. For example, organizing content, chunking, minimalism, re-use, etc. Individual contributor responsible for creating and maintaining end user documentation. Work with scrum teams and SMEs to create and validate documentation. Passion for research You enjoy conducting in-depth research to gather the necessary information for creating accurate and comprehensive technical documentation. Collaborative mindset You thrive in collaborative environments, actively seeking input and feedback from subject matter experts and cross-functional teams to ensure the highest quality documentation. Team player You are a valuable team player, capable of effectively collaborating with colleagues to achieve shared goals and objectives. Self-motivated You possess a strong internal drive and motivation, allowing you to work independently, meet deadlines, and consistently deliver high-quality results. Results-oriented You have a proven track record of delivering outcomes and achieving tangible results, demonstrating a results-oriented approach in your work. Passion for explanation You enjoy explaining complex technical concepts in a clear and understandable manner, ensuring that end-users can easily grasp the information provided. Dedication to simplification You are committed to simplifying complex ideas and processes, transforming them into user-friendly and accessible documentation. One Last Thing OpenTexts efforts to build an inclusive work environment go beyond simply complying with applicable laws. Our Employment Equity and Diversity Policy provides direction on maintaining a working environment that is inclusive of everyone, regardless of culture, national origin, race, color, gender, gender identification, sexual orientation, family status, age, veteran status, disability, religion, or other basis protected by applicable laws. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please contact us at hr@opentext.com . Our proactive approach fosters collaboration, innovation, and personal growth, enriching OpenTexts vibrant workplace.

Responsibilities: * Develop quality plans & procedures * Ensure compliance with ISO standards * Conduct final inspections & process audits * Collaborate on continuous improvement initiatives Annual bonus Health insurance Provident fund

Job Summary Quality Documentation specialist reviews vendor documentation to ensure compliance with purchase order and prepare/ review Customer document packet to ensure compliance to Customer Purchase order. In This Role, Your Responsibilities Will Be: Review and approve vendor Documentation -CMTR s (Chemical, Mechanical, NDE, Corrosion, Painting . . etc) by comparison with material specification to assure compliance with ASME Code , Purchase Order and Emerson Quality Assurance requirements. Contacts Suppliers of documentation on deficiencies by interface with Supplier Quality Management personnel to delineate and clarify specification requirements and recommend correction action. Responsible for the review and approval of Supplier Documentation to assure that all purchased material, equipment and services confirm procurement specifications. Prepares and reviews Customer documentation packet. Ensure they are compliant to customer PO before uploading to Emerson portal. Investigates and initiates necessary corrective actions for documentation related to Customer/ internal complaints and collaborates with respective parties for improvements. Implementation of new document management tools Perform other duties as assigned! Who You Are: You have good attention to details and can set priorities and follow up on actions. You understand the project execution process and have a passion for learning and continuous improvement and collaboration. You quickly and significantly act in constantly evolving, unexpected situations. You actively seek guidance from relevant sources to learn and upskill yourself. For This Role, You Will Need: Bachelors / Diploma in Mechanical / Metallurgy. A minimum of 3 years experience in preparation and review of document packets related to ASME, API or equivalent certified valves/ products. People Skills works well in a team environment and collaborates well with other colleagues Communicate effectively in English, in both written and verbal form. Preferred Qualifications That Set You Apart: Working knowledge in Material properties, NDE, Coatings, ASTM standards, & ASME Sec II/ V to support the review of the vendor documentation Exceptional knowledge in MS office tools (Excel, Word, PDF) Experience in ASME Code valve data packet preparation and review. Working knowledge in Valve manufacturing, assembly & testing. Must have the ability to respond effectively to the most sensitive inquiries, complaints, or Ability to recognize and solve problems of a complex nature Our Culture & Commitment to You . .

Accountable for ensuring the smooth functioning of the Quality function of the organization and availability of QMS and Tools on the intranet. Hands on experience in ensuring the effective implementation of the Organizational Quality processes. Health insurance Provident fund

Department: Quality Assurance / Quality Control Reports To: Quality Head - Plant Quality Manager Role Overview: We are seeking a detail-oriented and process-driven Assistant Manager - Quality Engineer to oversee and enhance quality assurance and quality control functions in our cable manufacturing facility. This role ensures adherence to internal standards and customer specifications while supporting continuous improvement in product and process quality. Key Responsibilities: Ensure compliance with ISO, BIS, UL, CE , and other regulatory and customer-specific standards. Monitor and analyze in-process and final inspection data for cables, ensuring defect-free product delivery. Lead root cause analysis (RCA) and corrective/preventive action (CAPA) for internal failures and customer complaints. Coordinate with production, R&D, and supply chain teams to drive improvements in material quality and process stability. Supervise quality inspectors and lab personnel in day-to-day inspection and testing activities. Maintain calibration of test equipment and ensure timely internal audits of quality systems. Implement statistical quality control techniques such as SPC, MSA, and FMEA . Prepare and maintain quality documentation, reports, SOPs, and control plans . Participate in customer audits, third-party inspections, and quality reviews . Support new product development (NPD) through qualification testing, trials, and validation. Provide technical support in raw material evaluation and supplier quality initiatives. Key Requirements: Education: B.E./B.Tech in Electrical, Mechanical, or Polymer Engineering (preferred). Experience: 4-8 years in quality function within the cable, wire, or polymer-based manufacturing industry. Strong knowledge of cable testing standards (e.g., IS, IEC, ASTM). Familiarity with lab equipment such as HV test sets, tensile testers, elongation testers, aging ovens, etc. Proficiency in tools like 8D, 5 Why, Fishbone Analysis, SPC, Minitab (preferred). Experience using ERP systems such as SAP for quality documentation and reporting. Ability to lead internal teams and interact confidently with customers and external auditors. Key Competencies: Attention to Detail & Analytical Skills Problem-Solving & RCA Quality Standards & Regulatory Compliance Data-Driven Decision Making Cross-Functional Collaboration Customer-Oriented Mindset Team Leadership & Communication Why Join Us? Be part of a quality-driven organization with a strong reputation in the cable industry. Take ownership of key quality improvement initiatives and work cross-functionally. Opportunity to grow into leadership roles in quality and operations.

Roles and Responsibilities Conduct quality inspections of sheet metal parts using measuring instruments such as Vernier caliper, Micrometer, Height gauge etc. Ensure compliance with welding processes and standards (e.g. AWS) through visual examination and testing. Develop and maintain documentation for quality control procedures, including QMS systems. Perform final inspections on products before packaging to ensure conformance to specifications. Collaborate with production teams to identify areas for improvement in manufacturing processes. Desired Candidate Profile 1-4 years of experience in Quality Engineering or related field (Sheet Metal industry preferred). Diploma/B.Tech/B.E. degree in Mechanical or relevant specialization.