660 Iso Documentation Jobs - Page 10

Job Description :- Implementation & Documentation of IMS Provide the training of company employee ( 7 QC tools, SPC,TPM, Implementation of QMS,5s, etc) Documentation of PPAP Monitoring & updations of FMEA Ensuring that processes needed for quality management system are established implemented & maintained. Conducting management review meetings & verifying the actions decided in the meeting. Conducting internal quality audits & preparing the summary of audit for presenting management review meeting & closure of non-conformities after verifying them Controlling of documents I.e., their approval issue & also controlling any amendments in existing documents or needs for any new documents. Ensuri...

Candidate will primarily assist senior engineers with design, developments & implementation of sheet metal components & systems. Inspect raw materials, in-process components. Maintain proper documentation of inspection reports. Required Candidate profile ITI / Diploma/Degree in Mechanical Engineering.

design quality, supplier quality, manufacturing quality and field quality, CTQ in respective areas of ODM operation, Ensure product & process approbations, Overall MR for ISO related certifications, IS & IEC quality standards for lighting products,

Sessions on various Quality/Management System Mentor & coach companies using Omnex methodologies, deployment. Best in class systems, Problem Solving, APQP/PPAP/FMEA/Lean 6sigma. Undertake consulting/training for clients to ensure certification audits

Lead QA across SMT & assembly lines, manage audits, drive root cause analysis, enforce ISO/IPC standards, mentor team, resolve customer issues, and champion continuous improvement at Vikin Electronics, Ahmedabad

Experience into machinery manufacturing industry Research and draft blueprints, engineering plans, and graphics Supervise the manufacturing process of all designs Estimate cost limits and budgets for new designs. Develop test prototypes Required Candidate profile Experience Autocad, solid edge, solid works. Use design software to develop models and drawings of new products.

Job Title: Quality Assurance Engineer / Senior Engineer QMS & Audits Function: Quality Assurance Location: Tirupathi, Andhra Pradesh Experience Required: 4 to 7 Years Education: B.E. / B.Tech in Mechanical Engineering, Industrial & Production, or Total Quality Management MBA or MS in TQM (preferred, not mandatory) Qualifications: Certified Internal Auditor as per ISO 19011 standard for IATF 16949 or AS 9100 D from an authorized institute or organization Industry: Aerospace, Automotive, Precision Engineering, Manufacturing Employment Type: Full Time, Permanent Job Summary: We are looking for a motivated and experienced Quality Assurance Engineer to join our team and strengthen our Quality Man...

ONLY MALE CANDIDATE CAN APPLY INTERVIEW WILL BE IN PUNE JOB LOCATION WILL BE PATALGANGA - RASAYANI, PANVEL Designation: Engineer / Assistant Engineer Department: Quality Reporting To: QA Lead Location: Patalganga - Rasayani. Fabrication Plant, Industrial Area, Maharashtra Role Objective : To support the setup and execution of quality assurance processes across the fabrication lifecycle, including release checks, WPS traceability, documentation control, and audit preparedness enabling right-first-time fabrication, weld traceability, and ISO/client compliance. Key Responsibilities : 1. Assist the QA Lead in preparing and maintaining fabrication ITPs (Inspection and Test Plans), release checkli...

DME/BE - Mech with at least 10-15 years of experience in automotive industries, Knowledge of IATF 16949,VDA 6.3, Pokayoke, Kaizen. Having ERP Knowledge shall be preferred.

Responsibilities: * Conduct internal process audits. * Maintain accurate records and reports. * Ensure compliance with ISO 9001, 14001, 45001, 13485 standards. * Collaborate with cross-functional teams on quality improvement initiatives.

Recruitment Training & Development HR Policies ISO Documentation Employee Engagement

Understand customer needs & requirements to develop effective quality control processes Supervise inspectors, Technicians Keep accurate documentation Handling OOS & OOT Preparation of Audit report Understand requirements of ISO 13485:2016 (MDQMS)

Lead all QA activities including incoming, in-process, and final inspection of precision, mechanical components and assemblies. Supervise the calibration management of the companies inspection and manufacturing equipment, including CMM's, precision instruments, welding sets etc Manage and ensure competency in NDT techniques including UT and Dye Penetrant Testing of welds. Coordinate with design, production, and supply chain teams to resolve quality-related issues. ISO 9001 Management & Compliance: Maintain and enhance the companys ISO 9001:2015 Quality Management System. Conduct internal audits and prepare for customer and third-party audits. Ensure compliance with applicable quality standar...

Looking for Candidates who will be responsible for : QMS : Lead, maintain, and continually improve the companys Quality Management System in line with IATF 16949 and ISO 9001 requirements. Plan, execute, and monitor internal system audits per audit program; ensure auditor competency and closure of non-conformities. Facilitate management review meetings with actionable insights and data-driven inputs from core business processes. Ensure robust document and record control system as per standard; manage changes and version control across the organization. Ensure readiness for third-party and customer audits; lead responses to NCs and drive certification maintenance and renewals. Define and trac...

Responsibilities: * Maintain documents as per ISO audit point of view. * ISO based documentation and QMS maintain. Provident fund Health insurance

As a QA Assistant Manager with 5-7 years of experience in the pharmaceutical industry, you will be responsible for running the department independently. Your role will require strong skills in inter and intra-departmental communication, a desire to learn, and the ability to adapt and adopt to people and systems effectively. This position is based in Mumbai. Your key responsibilities will include: - Skilled handling of FDA-GMP audits to ensure compliance with regulatory standards. - Experience in establishing robust Quality Management Systems (QMS) to ensure compliance with GLP and cGMP standards. - Expertise in creating, reviewing, and maintaining Standard Operating Procedures (SOPs). - Mana...

Role & responsibilities 1. Leading Audit Program (MACE AUDIT, IATF 16949:2016, and CUSTOMER PROCES & SYSTEM AUDIT) of the company. 2. Ensure that processes needed for Quality Management System are established, implemented & maintained (e.g., Control of documents, Internal Auditing, MRM.) 3. Ensure implementation of various types quality standard throughout the plant for new products as per customer requirement. 4. Responsible for implementation of all procedure described in quality management system. 5. Responsible for ensuring that all In-House systems and procedures are updated revise and modified to meet the external certification bodies. 6. Responsible of verification and approval for ma...

Hello, Position : PPC Engineer (NPD) Qualifications : Dip, Degree Mechanical Skills : Production, Planning, New Product Development, Quality Plan, Documentations, PPC Module Email : rghrsolutions2@gmail.com Thanks, Vijay G Shinde RG HR Solutions

Ensure ISO documentation compliance, read mechanical drawings, use measuring tools, understand basic GD&T, and report quality issues accurately. Good observation, reporting, and basic computer skills required. Apply: hr@cogmac.com Provident fund

Position Purpose: Implement site EHS goals. Implement the occupational health, safety and environment functional requirements under the guidance of EHS Head to strategically achieve Organizational EHS Goals. Ensure that the projects, processes and operations of the organization are being performed in compliance with various acts, rules and applicable legal conditions while ensuring fulfillment of IMS and ESG requirements. Key AccountabilitiesRole DescriptorsIMS Implementation and Sustenance Responsible for implementation and management of documentation structure for ISO 9001:2016, ISO 14001:2016 and ISO 45001:2018 as Integrated Management System (IMS) for NEPRA. Responsible to conduct Intern...

We are Hiring for VP Quality for our Prestigious Electronics Component Manufacturing with High Precison Plastic and High Metal Component Consumer Electronics. Job Title: Vice President Quality Location: Oragadam, Chennai, Tamil Nadu, India Department: Quality Assurance & Regulatory Compliance Reports to: Chief Operating Officer / CEO Expereince 18 to 24 Years in Electronic Component Manufacturing / EMS We specialize in the manufacturing of high-precision components that meet the exacting demands of global industries including automotive, electronics, aerospace, and medical devices . Our advanced capabilities in micro-machining, ultra-tight tolerance control, and high-speed automation enable ...

Job Summary: We are seeking a highly experienced and qualified Senior ISO Consultant to lead, manage, and support consultancy and audit projects across multiple ISO standards including ISO 9001 (Quality), ISO 14001 (Environmental), ISO 45001 (Occupational Health & Safety), ISO 27001 (Information Security), and ISO 37001 (Anti-Bribery). The candidate should be capable of managing multiple clients, conducting gap analysis, implementing systems, training stakeholders, and supporting external audits. Key Responsibilities: Lead and implement ISO management systems for clients across ISO 9001, 14001, 45001, 27001, and 37001. Conduct gap assessments, risk assessments, and internal audits. Prepare d...

Perform in-process & final quality inspections Maintain ISO documentation & support audits & compliances Identify & resolve quality issues Root cause analysis, implement corrective actions Ensure product quality in coordination with production teams Required Candidate profile 3–5 years experience in engineering company/ fabrication & machine shop operations Knowledge of ISO implementation & documentation Proficient in inspection tools & interpreting engineering drawings

Overall handling of Quality Procedures & Quality Management System (QMS). Handling & Issuance of NCs, CAPA and Change Control. ISO Audits, PDI, BMR, Audit Documentation, Customer Audits Required Candidate profile BE/ Btech/ Diploma- Mechanical Engineering, Min. 1 year exp as Quality Executive/ Engineer in Medical Devices or Automotive Industry. Prior exp of handling Quality Procedures & QMS, CAPA, Audits.

Plan, execute & close quality system audits & submit them 2 customer as per requirements.IMDS[International Material Data System], SOC[Source of Contamination],Core QMS, VDA 6.3, Excellent knowledge of IATF,ISO 14000/ 45001.Sound interpersonal skills Required Candidate profile Organize meetings on company rules & regulations & amend/modify as needed.Lead training sessions on company's guidelines.Maintained change & revision history of documented quality system information