741 Quality Documentation Jobs - Page 16

Manager / Sr. Manager Quality & Clinical Testing Godrej Pet Care Nashik ———————————————————————————————————— About Godrej Industries Group (GIG) At the Godrej Industries Group, we are privileged to serve over 1.1 billion consumers globally through our businesses with market leadership positions in the consumer products, real estate, agriculture, financial services and chemicals industries. Read more: https://www.godrejindustries.com/ Introducing Godrej Pet Care: A New Chapter in the Pet Foods Industry We are excited to announce the launch of Godrej Pet Care (GPC), a 100% subsidiary of Godrej Consumer Products Limited, that’s set to make a mark in the thriving pet food industry. The pet food ...

As a Quality Assurance/Quality Control professional, you will be required to have a minimum qualification of Diploma in Mechanical Engineering (DME) along with at least 5 years of relevant experience in QA/QC roles. Your responsibilities will include ensuring compliance with relevant standards such as ISO, ASNT, IS, etc., and familiarity with industry standards and best practices. You will be expected to demonstrate proficiency in quality documentation and reporting, as well as possess knowledge of handling different kinds of quality instruments. This is a permanent position that requires you to work in person at the specified location.,

Conduct on-site inspections, audits and assessments to ensure compliance with industry standards and client specs. Document findings, prepare detailed reports and coordinate with clients and internal teams for effective quality assurance. Required Candidate profile Willingness to travel extensively. Good understanding of electrical systems, instrumentation principles & basic testing procedures. Strong report writing, documentation, and communication skills.

The position involves Project Management at sites, encompassing Quality documentation, Surveillance, and Expediting as a part of EPC contractor's engineer & inspection of various items for Projects. You will be responsible for preparing quality documentation aligning with project specifications, codes, and standards, and obtaining approvals from PMC/Client. Coordinating with Client/PMC/EPC for daily activities concerning Field quality & documentation is a crucial aspect of this role. It is essential to ensure services are performed in accordance with the End user/PMC/EPC Quality Assurance System/ISO 17020 requirements, including the BV Code of Ethics and BV Group policy. To be considered eli...

Hospital background with strong data analytical skills Skilled in Power BI, Excel, dashboarding & KPI tracking Experience in clinical workflows, quality & documentation Ideal for hospital analytics, operations & reporting roles

Job Purpose To provide quality support to all projects, quality engineers and analysts involved in Manufacturing and Production Operational Activities. Quality Improvement Initiatives To support an environment where Quality Employees support maintaining and improving flow, and create the required Quality behavior within those relationships. To create LEAN / Continuous Improvement thinking within the team, and validated by Improved Performance Results. Work under minimal guidance to ensure TechnipFMC''s Product are manufactured in accordance with TechnipFMCs Quality Management System, Business Processes and Client requirements. Effectively collaborating with various departments and clients to...

The APU Quality Leader position coordinate Quality members inside the APU, coordinate process and product audit, train and coach the Logical Thinking. This position cannot supersede Site Quality Manager authority. Initiate the QRQC in QIM database participate to the containment and validate the robustness of the containment Support APU Managers / Site Manager in the analysis of issues assigned in the QRQC activities Update the APU quality tracking charts : Customer Returns Cost of Non Quality Perform audits on the line to detect non-respect of the Standard and identify with the APU the actions to be completed to therefore comply with the Standard Participate in the eradication of Customer is...

Post- Quality Documentation Specialist Location - Pune Chakan Contact - 9356395439 Email - punejob2025@gmail.com Experience - 05-10 yrs Skills Certification in ISO 9001:2015 Internal Auditor or Lead Auditor. Prior experience in the renewable energy or heavy fabrication sector. Knowledge of ISO 45001 and ISO 14001 standards. Strong knowledge of APQP, PPAP, FMEA, Control Plans, and Process Flow Diagrams. Experience with ISO 9001 audits and OSHA safety documentation standards. JD Quality Documentation Specialist to manage and improve our documentation systems in line with industry standards. The ideal candidate should possess hands-on experience with PPAP, APQP, ISO audits, and OSHA documentati...

We are seeking a knowledgeable and detail-oriented IRIS Audit Specialist to oversee and execute Quality Management System (QMS) audits in alignment with the International Railway Industry Standard (IRIS) , specifically ISO 9001 and ISO 22163 . The ideal candidate will bring a solid understanding of quality principles, railway industry standards, and auditing techniques. They will play a key role in planning, conducting, and reporting IRIS audits and guiding continuous improvement initiatives within the organization. Key Responsibilities: Plan, schedule, and conduct internal IRIS audits in accordance with ISO 22163 and ISO 9001 standards. Use the IRIS Audit Tool and Portal for accurate audit ...

Responsibilities: * Conduct quality audits using ISO standards * Ensure compliance with PPAP documentation requirements * Maintain accurate computer records for quality management systems Provident fund

Post - QMS -Manager Qualification : BE Electrical or Electronics Location Pune chakan Contact - 9356395439 Email - jobpune12@gmail.com Experience : 5 + yrs experience in control Panel manufacturing Salary : No bar for the right candidate. QMS Development and Implementation: Establishing and maintaining the QMS according to relevant standards like ISO 9001, AS9100, or IEC 61439-1 & 2, as applicable. Compliance: Ensuring adherence to all relevant standards, regulations, and customer requirements. Documentation: Managing and controlling QMS documentation, including procedures, work instructions, and control plans. Audits: Conducting internal audits, coordinating external audits, and managing re...

Job Responsibilities Operations Build successful relationships with Life Sciences (LS) client stakeholders to promote confidence in quality and compliance, as well as forward planning. Provide management and leadership direction for the development and implementation of quality and compliance programs. Collaborate with other Life Sciences accounts to proactively accumulate, share and reapply all learnings, successes as well as best practices. Collaborate with Global Life Sciences Quality Vertical for development, revision and implementation of QMS and quality documents. Responsible for ensuring Lide Sciences facilities teams adhere to the required training and ensuring in compliance to clien...

Responsibilities: * Conduct quality inspections & audits * Ensure compliance with quality standards * Manage raw material inspections * Oversee quality control processes * Monitor product quality throughout production cycle

Track and Trace Analyst Job Description Your Job Do you thrive in fast-paced environments where coordination, communication, and precision are keyDo you love solving logistical puzzles to create smooth, on-time deliveries At Kimberly-Clark Professional (KCP), were looking for a Track & Trace Analyst to join our North America Customer Care team. In this role, you ll be the critical connection point between customers, transportation partners, and internal teams ensuring every shipment is tracked, every exception is resolved, and every delivery meets customer expectations. Youll lead initiatives, tackle complex problems, and make real impact on the customer experience. About Us Huggies . Kleene...

Role & responsibilities 1.Issurance of BMR,ECR to production Department. 2. Issuance ofprotocol to QC deparlment & other formats to respective department. 3. Issuance offinished product labels and seal. 4. To maintain, check and retention fi1led BMR, QC reports, formats and other filled records that are received from production, quality control and other departrnents. 5.To issue and Handling of change control,deviation,OOS reports and maintain their records. 6.To co-ordinate durins intemal audit. 7. To take QA round or as per SOP's. 8. To do any other supporting work in absence of any other staff from department as per instructior given by department head. 9. To prepare and review master doc...

Job Title: Asst. Manager / Manager Quality Control Department: Quality Control Number of Opening – 1 Nos Experience Required: 5 to 10 Years Location: At Factory – Daheli, Valsad, Gujarat Reports To: Quality Head Job Purpose: To ensure that all raw materials, in-process production, and finished goods meet the required quality standards. The QC Manager is responsible for implementing and maintaining quality systems, reducing rejections, and ensuring customer satisfaction through consistent product quality. Key Responsibilities: 1. Quality System Implementation: Develop, implement, and maintain quality control procedures and inspection plans. Establish and monitor quality parameters (bursting s...

Job Summary: The Documentation Engineer will be a key member of the execution team, responsible for managing and maintaining documentation related to installation, commissioning, and qualification of process and utility equipment. This role is ideal for mid-level professionals (3-5 years of experience) looking to advance their expertise in installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ) for equipment used in pharmaceutical, chemical, and food processing industries. Key Responsibilities: Prepare and maintain IQ, OQ, PQ documentation for micronizing mills, containment isolators, bulk handling systems, and fluid bed dryers. Ensure documentatio...

Key Responsibilities: 1. Quality Management System (QMS): Establish, implement, and maintain ISO 9001, ISO 14001, ISO 45001, and ISO 50001-compliant QMS. Ensure documentation, internal audits, CAPA, and system updates are regularly reviewed and improved. Ensure compliance with BIS, IEC, and MNRE guidelines. 2. Quality Assurance & Control: Define quality parameters and inspection plans for raw materials (glass, EVA, backsheet, cells), in-process components, and finished modules. Supervise QA/QC operations across all stages incoming material inspection, in-line process checks, and final testing. Manage electroluminescence (EL), IV testing, Hi-pot, insulation resistance (IR), and thermal cycle ...

As an experienced professional with over 3 years of experience in Computer System Validation (CSV) and IT quality assurance within regulated industries such as pharmaceuticals, biotechnology, or medical devices, you will be responsible for developing, executing, and documenting CSV protocols and reports for both new and existing computer systems and software applications. Conducting risk assessments and gap analyses will be a key part of your role to identify potential quality issues and implement necessary corrective actions. Your responsibilities will also include developing and maintaining quality documentation, such as Standard Operating Procedures (SOPs), validation plans, test cases, a...

Actively monitoring and ensuring the quality of products being assembled on a production line by performing regular inspections, identifying defects, implementing corrective actions, and collaborating with production teams to maintain high quality Required Candidate profile Candidate have Good Expereince in Assembly line Either Genset industry Interested Candidates can send their resume on hdinavdeep@gmail.com

Role & responsibilities Lead and manage Incoming (IQC), In-Process (PQC), and Final Quality Control (FQC) processes. Interface with customers, vendors, and cross-functional teams for quality audits, inspections, and approvals. Champion Root Cause Analysis (YY analysis) and drive implementation of effective Corrective and Preventive Actions (CAPA). Ensure compliance to Defense and Aerospace quality standards in design, development, and manufacturing stages. Maintain and continuously improve QMS documentation including SOPs, work instructions, inspection reports, and quality plans. Lead internal and external quality audits, certifications, and statutory compliance. Facilitate cross-departmenta...

Role & responsibilities * Creating and maintaining quality control processes, policies, and standards. * Tracking and analyzing quality control data to identify trends, root causes, and areas for improvement. * Supervising and mentoring quality control personnel, providing guidance and support. Working with various teams, departments, and stakeholders to align quality control efforts with business objectives. * Identifying opportunities to enhance product quality and production efficiency. * Maintaining accurate and up-to-date quality control documentation. Preferred candidate profile 10-15 years of experience in the valves/fittings industry, preferably with ADNOC, ARAMCO, KOC, etc.

Build Con is seeking a highly experienced and meticulous Head of Quality Control to lead the quality assurance and control operations at our Ready Mix Concrete (RMC) plant in Dombivli. This role is pivotal in ensuring that all concrete produced meets the highest standards of quality, adhering to IS codes, client requirements, and statutory regulations. Key Responsibilities: Lead and manage the entire Quality Control (QC) function of the RMC plant. Develop, implement, and monitor concrete mix designs in line with IS standards and project specifications. Oversee routine testing of raw materials (aggregates, cement, admixtures, water) and finished concrete to ensure consistency and compliance. ...

Maintain compliance with medical textile standards. Coordinate with production to maintain product quality. Train workers on hygiene, GMP, and quality SOPs. Good understanding of medical garment standards. Attention to documentation.

1. Looking for Graduate Engineer with 6-8 years of experience in QA department of an engineering or FMCG company. 2. Shall be well versed with ISO 9001, ISO45001 and willing to take responsibility for setting up the QMS. 3.Person possessing knowledge about TQM with experience in implementing POKA-YOKE is preferred. 4. Should have experience of documentation of audit process.