383 Iso Documentation Jobs - Page 8

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

Develop and implement quality assurance protocols and procedures Conduct inspections and tests to ensure product quality Maintain documentation and records as per industry standards Ensure compliance with IATF 16949:2016 and other relevant standards Required Candidate profile Bachelor's degree in Engineering or related field. 5–6 years of experience in QA . Strong understanding of quality control standards and methodologies

Job description ISO 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 client’s factory is required at your & client’s mutual convenience. Schedule : Flexible shift Education: ( Any of the following) 1. Any Gradutate with knowledge of ISO consultancy/ISO Auditing/ Quality Related fields 2. Any Graduate with minimum 8 years industrial experience in manufacturing. 3. Diploma with 10 years industrial experience in manufacturing 4. BE/BTech with 8 years industrial experience in manufacturing 5. Knowledge of ISO &/or Lean tools implementation/Documentation/Consultancy/Systems/Quality related fields shall get additional weightage Place of Posting:- Shall be required to cover industries near your residence to provide onsite/ Offsite consultancy in factories. Roles and Responsibilities :- 1. To provide onsite and offsite consultancy to the MSME manufacturing clients for doing ISO 9001/14001/45001 consultancy at client’s site and offsite. 2. Same Consultants shall be trained to provide ZED consultancy of the Central government scheme of Zero Defect Zero Effect (ZED) promoted by Ministry of MSME. 3. Same consultants shall also be trained to provide consultancy for lean tools under MCLS MSME Competitive (Lean) Scheme promoted by government of India. Training :- 1. The candidate shall be trained by our company so that he can pass an online examination of Quality Council of India (QCI) to become a national level approved ZED certified consultant and subsequently trained to become national level approved MCLS certified consultant. 2. After clearing the online exam, the consultant shall be allotted MSME manufacturing clients by our company for implementation of ZED scheme. 3. ZED consultant shall be required to implement the ZED &/or lean techniques / modules to help the client obtain ZED/MCLS certification as per the guidance of our company. 4. Consultant shall be provided regular training, support and guidance from the head office so that the ZED/MCLS modules can be implemented properly at client’s factory and ZED &/or lean certificate is delivered in time. Perks and Benefits: 1. Performance incentives Like New Laptop, New Mobile, New Inverter for your residence after starting at least 3 projects as per company norms. 2. No outstation travel required 3. Cell phone reimbursement 4. Flexible schedule 5. Internet reimbursement ABOUT THE COMPANY – BMCPL Boon Management Consultants Pvt. Ltd. (BMCPL) is a consultancy organization (Incorporated in 2005) that specializes in providing services for improvement of systems including capacity building, implementation of lean tools, ZED Consultancy etc. BMCPL is providing consultancy and training services to it’s clients all over India through our consultants located pan India. Besides many private and services sector clients , we are providing services to government/semi-government organizations. Some of our government clients are 33 ZILLA PARISHADS, RURAL DEVELOPMENT DEPARTMENT- GOVERNMENT OF MAHARASHTRA, OFFICE OF GOVERNOR OF MAHARASHTRA, etc. For the ZILLA parishad project done by us, RURAL DEVELOPMENT DEPARTMENT (RDD) has won National Award. MoMSME has selected Quality Council of India (QCI) which is an autonomous body under Govt. of India for implementing and Monitoring ZED scheme across India. QCI has selected BMCPL as a ZED consulting organization and also for MCLS consulting organization for pan India operations. About the ZED Scheme: The Ministry of MSME has selected the Quality Council of India (QCI), an autonomous body under Govt. of India to implement and Monitor the ZED (Zero Defect Zero Effect ) scheme across India. QCI has selected BMCPL as a ZED consulting organization for pan-India operations. The majority of the fees for this project shall be paid by govt. (Ministry of MSME/QCI) and negligible cost shall be borne by the client.The details of the scheme can be seen on govt. website zed.msme.gov.in Till date Boon has trained 150+ ZED consultants and 40+ MCLS consultants from different parts of India Like Maharashtra, West Bengal , Gujrat, Telangana, Tamil Nadu, AP, Karnataka, etc. The consultants have passed the Quality Council of India Examination and have received ZED Consultant certificate. BMCPL has 700+ MSME clients who have taken Pledge to become a ZED certified organisation. Out of this 500+ MSME clients have already received ZED Bronze certification, 200+ clients have received ZED Silver certification and others are in process to get ZED Silver/Gold certification. BMCPL has 100+ MSME clients who have taken pledge to do MCLS and out of this more than 50 MSME clients have received MCLS BASIC level certificate.

B.Tech Chemical, M.Sc Chemistry, B.E Environment and Must have ADIS/PDIS Skill Required for you to qualify for role ISO Implementation (ISO 9001, 14001, 45001), ISO Audit, ISO Documentation, HIRA, HAZOP Your Role at Luthra Group Role and responsibilities Review Site IMS documents, SOP preparation, and records and labelling. Ensure compliance with ISO 9001:2015; ISO 14001:2015, ISO 45001:2018 standards and regulatory guidelines. Oversee data digitization and record-keeping of O&M manuals and drawings. Manage Gensuite applications, User-IDs, Permissions and Monitor Site wise Gensuite App progress, including generating statistics, presenting data, and training staff. Address Gensuite errors, and handle Gensuite APP enhancement lists. Compile and follow up on internal and external audit findings. Prepare audit checklists and ensure compliance tasks are assigned and completed at different sites. Review Corporate and Site documents, records. Ensure Green Certified products are procured and used at certified sites.

Role & responsibilities Develop, assist, implement, and maintain robust documentation in line with international standards. Collaborate with clients to implement best practices and optimize processes. Coordinate during training sessions on ISO compliance and regulatory updates. Work with cross-functional teams to enhance quality assurance frameworks. Conduct internal audits for systems like QMS, EnMS, etc. Preferred candidate profile ISO standards and certification process understanding. Auditing, compliance, and documentation experience. Strong communication and training skills. Analytical, detail-oriented mindset. ISO Lead Auditor certification (preferred).

Roles and Responsibilities Ensure compliance with quality management systems (QMS) through implementation, maintenance, and continuous improvement of ISO documentation. Prepare SOPs for various processes such as BMR, CAPA, Change Control, Cleaning Validation, etc. Conduct qualification testing and validation protocol execution to ensure product quality and regulatory requirements. Develop and maintain accurate records of test results, reports, and certificates related to quality assurance activities. Collaborate with cross-functional teams to identify areas for improvement in quality control processes. Desired Candidate Profile 5-10 years of experience in pharmaceutical industry with expertise in QMS implementation. Strong understanding of GMP regulations and industry standards like ISO 9001:2015. Proficiency in preparing documents like BMR, SOPs, Capas, Change Control procedures. Experience with cleaning validation process validation protocol execution.

Key Roles and Responsibilities Prepare manuals, SOPs, and work instructions without errors. Conduct internal audits for IMS as per ISO 9001:2015, ISO 14001:2015, and ISO 45001:2018. Perform facility and 5S audits. Assist and guide departments in implementing 5S practices. Create and maintain documents as per RJC requirements. Prepare presentations and monthly review meeting reports. Explain processes or concepts in detail. Analyze problems and find solutions. Understand and apply standards and requirements. Be a self-learner and strive for continuous improvement. Work with a result-oriented mindset. Be self-motivated with a professional and ethical approach. Collaborate well with team members. Educational Qualifications & Experience Any UG degree or diploma with relevant experience 0-6 Years Experience Proficient in MS Office, Root Cause Analysis (RCA), and Corrective Action Preventive Action (CAPA). Experience working with ISO standards is essential. Strong communication and presentation skills. Fluency in English, Tamil, and Hindi (preferred). Good analytical and problem-solving skills. Detail-oriented with a focus on continuous improvement. Team player with a positive attitude. If you are interested in this position, please reach out directly at 8056907222 / 8056923339 or share your resume at sanjay.m@ejindia.com.

Responsibilities: * Ensure compliance with ISO standards through documentation and audits * Conduct system audits and document findings * Develop and implement QMS policies and procedures

Our Client a reputed 60Yrs Chemical Company needs - Post : QC In-Charge Location :Palghar Experience : Min 15 years of experience in QC. Qualification : M.Sc. Chemistry / B.Tech in Chemical or related field Salary : 15 LPA Job Profile: Should have thorough experience in laboratory of chemical manufacturing unit. Operation/calibration of analytical instrument. Analysis of raw material. Water analysis. Lead the QC team and manage all quality control activities across the plant. Ensure timely and accurate testing of raw materials, in-process, and finished products. Coordinate with production, QA, and R&D teams to ensure consistent quality. Ensure calibration, maintenance, and proper functioning of QC instruments. Skills: Strong knowledge of chemical analysis and lab/QC techniques. Leadership and team management. Root cause analysis and problem-solving. Documentation and report writing. Attention to detail and quality mindset. Email CV with current salary and notice period to resume@jobspothr.com All job updates on www.jobspothr.com Call 99877 06721 / 83697 08611 after mailing CV Good Luck !

Our Client a reputed 60Yrs Chemical Company needs - Post : QC In-Charge Location :Palghar Experience : Min 15 years of experience in QC. Qualification : M.Sc. Chemistry / B.Tech in Chemical or related field Salary : 15 LPA Job Profile: Should have thorough experience in laboratory of chemical manufacturing unit. Operation/calibration of analytical instrument. Analysis of raw material. Water analysis. Lead the QC team and manage all quality control activities across the plant. Ensure timely and accurate testing of raw materials, in-process, and finished products. Coordinate with production, QA, and R&D teams to ensure consistent quality. Ensure calibration, maintenance, and proper functioning of QC instruments. Skills: Strong knowledge of chemical analysis and lab/QC techniques. Leadership and team management. Root cause analysis and problem-solving. Documentation and report writing. Attention to detail and quality mindset. Email CV with current salary and notice period to resume@jobspothr.com All job updates on www.jobspothr.com Call 99877 06721 / 83697 08611 after mailing CV Good Luck !

Position: Head - Quality Location: Raipur, Chhattisgarh Industry: Steel (Texmaco Rail & Engineering Ltd.) Role Summary: Lead the quality function at Raipur Steel Foundry, ensuring products comply with customer specifications, statutory requirements, and internal standards. Responsible for developing and executing quality strategy, system implementation, audits, customer interactions, and continuous improvement. Key Responsibilities: Develop, implement, and monitor quality systems and policies Oversee QA/QC teams and drive adherence to quality objectives Lead root cause analysis and corrective action plans Coordinate with customers and third-party auditors for product approvals and audits Manage certification and recertification processes (ISO/IATF) Promote a culture of quality across the organization Qualifications: BE/B.Tech in Metallurgy or Mechanical Engineering 15+ years in Steel / Foundry quality functions, with at least 5 years in leadership roles In-depth knowledge of quality tools, SPC, ISO standards Strong leadership, problem-solving, and communication skills

Roles and Responsibilities : Ensure General and Preventive Maintenance of Plant Machinery & utilities. To lead for engineering function for entire site including project planning, New project execution and maintenance etc. Preparation of monthly engineering reports and effective monitoring of energy resources for reducing energy cost and monitor the manpower and accurate utilization for completing departmental tasks. Responsible for Calibration, Validation, Qualification Protocol & Reports. Operation & maintenance of HVAC BMS system . To work as per cGMP guidelines and upkeep the HVAC facility and all-time readiness for audit. Implementation of periodical servicing, annual maintenance, and other Engineering related works Should have practical knowledge of electrical-mechanical industrial engineering equipment installation & commissioning, Should be well equipped with Operation & maintenance, process piping, utility equipment & HVAC Installation & commissioning. Developing and Managing contract with vendor,ensuring timely availability of equipments, Spare parts, services and consumable to facilitate smooth execution. Execute activities & deliverables and prepare weekly and monthly reports. Execute GEP documentation like qualification, validation, change management, Project management and other quality-related engineering documentation. Lead work area and ensure personal safety and whole execution activity should be performed as per site safety compliance and procedures. Well knowledge of ETP plant and AHU operation is preferred. Work in Autocad, and other QMS softwares. To use the problem-solving tools to find out the root cause of any failure and implement the CAPA accordingly. Also has to take care of the operation and maintenance of remaining utilities like Chillers, hot water pumps, cooling towers, air compressors, Boilers, Water systems, ETP, Fire pump house, Electrical systems, safety compliance activities. Knowledge Required 1. 10-12 years of experience in Formulation Pharmaceutical Plant. 2. Minimum of 10-12 years of experience with Electrical & Mechanical installation, calibration, troubleshooting, HVAC O&M and Area Validation. 3. Computer proficiency in AutoCAD, MS Office, Excel, e-mail and internet functions.

Responsibilities: * Develop quality procedures & documents * Conduct regular audits & inspections * Ensure compliance with ISO standards * Implement quality management system Provident fund

Responsibilities: * Ensure compliance with quality standards & regulations * Conduct regular audits & inspections * Develop & implement quality procedures * Monitor product/service performance * Maintain accurate documentation Annual bonus

Responsibilities: Lead factory ops, ensure GMP compliance & ISO doc prep. Collaborate with R&D on new product launches & scale-up plans. Oversee API manufacturing processes & quality control measures.

Responsibilities: * Fabrication of piping, tanks, vessels. Material handling. Knowledge of Materials SS-Super duplex/SS 316/SS304, CS & other. * ISO documentations as per specific requirements. * RO/UF/NF/MF system manufacturing experience. Provident fund

The main purpose of this role is to carryout & perform all related activities to create Safety Culture and Krishnapatnam Factory as injury free and safe place to work for all categories of people. Main Accountabilities Advise and assist the Plant management in the implementation of EHS obligations, statutory and Bunge Global Safety Management system guidelines concerning prevention of personal injuries and maintaining a safe working environment. Promote setting up of safety committees and act as adviser and catalyst to Safety committees Administers the entire safety program ensuring safety compliance by the Plant team and all employees and subcontractors working at the site. Design and conduct suitable training and educational programmes for the prevention of personal injuries and for the propagation of safety awareness. Carry out plant safety inspections in order to observe the physical conditions of work and the work practices and procedures followed by workers and to render advise on measures to be adopted for removing the unsafe physical conditions and preventing unsafe actions by workers Advise the concerned departments in planning and organising measures necessary for the effective control of personal injuries Compiling HSE statistics and reporting to Plant management / Bunge India Safety Manager on a monthly basis Investigation of industrial accidents and occupational diseases and near-miss incidents Advise on safety aspects in all job studies and to carryout detailed job safety studies of selected jobs Check and evaluate the effectiveness of the action taken or proposed to be taken to prevent personal injuries Advise the purchasing and stores departments in ensuring high quality and availability of personal protective equipment Organise campaigns, competitions, contests and other activities which will develop and maintain the interest of the workers in establishing and maintaining safe conditions of work and procedure Maintain ISO & Bunge EHS Documentation Observe the Unsafe Conditions, Unsafe Act and Violation of safety Rules in the plant to initiate action for rectification by Technical Team Ensure and close monitoring of Work Permits System and Co-ordinate, Assess and give Safety Clearance for plant maintenance activities Make sure that safety features are in-built at the initial stage of new projects and inspect / recommend rectification on a continual basis Ensure regular Internal EHS audits / Inspections are carried out and regular follow up of external EHS audits / Inspections observations Conduct Safety Committee meeting, Fire drills and Mock drills on regular basis Monitoring the Workplace on Industrial Hygiene and suggest the control methods Carry out planned Safety Inspection and Risk Analysis and draw action plan Knowledge and Skills Behavior Use knowledge of Bunge's business, structure and strategy to develop innovative solutions to improve results or eliminate problems Build partnerships, appropriately influence to gain commitment, foster talent and coach others to grow in current or future roles Drive results through high standards, focus on key priorities, organization, and preparing others for change Technical Having the discipline and general management skills to make sure that people follow the standard processes and procedures Setting reasonable, challenging and clear expectations for people, and holding them accountable for meeting the expectations Team building skills so that the people work together well and feel motivated to work hard for the sake of the project and their other team members Proactive verbal and written communicator skills, including good, active listening skills Strong Technical Analytical, Communication skills and Presentation skills Ability to work under pressure Lead by example Good Team Player Education & Experience Degree / Diploma in Engineering with a Safety Diploma from RLI/CLI/any course approved by Andhra Factory Inspectorate for the appointment of Factory Safety officer as per relevant law Proficiency in Telugu is a Must Work Experience: 5-8 Years, preferably from Edible oil / Chemical Industry / MNC would be advantage but not essential Skill: Knowledge of SAP & MS Office skills

Ensure compliance with ISO standards & audits Conduct internal/external audits and vendor inspections Handle client meetings, pre-bid coordination, and customer complaints Monitor NCRs, statistical reports, and ensure project QA/QC effectiveness Required Candidate profile Must be Level-II in RT / UT as per EN ISO 9712 Monitor statistical method reporting. Discipline: -Electrical Engineer or equivalent Experience: - 5 to 7 years (Male or Female)

About the Role Were launching a new precision machining unit and are looking for a hands-on, experienced Production Manager to lead the charge. If you are passionate about CNC/VMC operations, process excellence, and leading shopfloor teams, this is your opportunity to build and lead a new plant from the ground up . Bonus If You Have Greenfield plant setup or commissioning experience Six Sigma, Lean, or TPM certifications Exposure to cross-functional leadership (Quality, Maintenance, SCM) Why Join Us? Be a founding member of our new precision machining unit Lead a high-visibility, high-impact project from day one Collaborate with a forward-thinking leadership team focused on quality and innovation Role & responsibilities What You'll Do Plant Setup & Operations Lead the commissioning of CNC/VMC machines (4-axis, turn-mill etc.) Plan and execute machining operations to meet production, quality, and delivery targets Ensure effective resource utilization: manpower, machines, and tools Team & Process Management Manage operators, supervisors, and cross-functional teams Train and mentor, the team in best practices, TPM, and 5S Enforce process discipline and build a culture of quality on the shopfloor Technical & Continuous Improvement Implement TPM, ISO/IATF-16949, and Lean Manufacturing principles Lead VAVE, productivity improvement, and cost optimization projects Develop jigs/fixtures in coordination with design and NPD teams Capex & Project Leadership Assess equipment needs and prepare CAPEX proposals Lead internal projects for machinery procurement and setup Support prototyping to serial production transitions in collaboration with customers Preferred candidate profile What You Bring Bachelor's in Mechanical / Production / Industrial Engineering 3-6 years in precision machining, 23 years in a leadership role Hands-on experience with CNC/VMC machines and Fanuc controls Strong knowledge of ERP, tooling, CAD/CAM, and quality systems (ISO/IATF)

Technical/Functional Skill Set: Inspection PCBA, Mechanical , Cables Accountable for ensuring the smooth functioning of the Quality function of the organization and availability of QMS and Tools on the intranet. Accountable for ensuring the effective implementation of the Organizational Quality processes. Defect Tracking & Analyzation Job Description: Developing and implementing quality control systems. Ensure effective co-ordination across groups / Groups to ensure effective QMS implementation and practice of processes. Regular update meetings with Groups to ensure effective process implementation and suggest any changes required. To assist project Groups in reviews and testing tracking for all assigned projects Sustenance of ISO 9001:2016 & AS9100 D certification for Organization and contribute towards continuous process improvement. Initiating Project Kick-off Meeting Project Planning and Tracking Monitoring of Project Reviews and Testing Activities Assist in Internal Audits and Corrective Actions / Closure of NCs Initiating Project Closure Process Monitoring and analyzing quality performance. Collection of data for Metrics and Analysis Collaborating with operations managers to develop and implement controls and improvements. Working with customers and quality agencies for Physical inspection, testing and final delivery Ensuring that workflows, processes, and products comply with safety regulations. Desired Skill Set: Inspection & Process Compliance. Good Excel, Macro will be an added advantage.

Role & responsibilities Implement and monitor QMS in line with ISO 9001 and BIS standards. Conduct internal audits and coordinate ISO certifications. Oversee inspection/testing at raw, in-process, and finished stages. Analyze data and drive corrective actions (CAPA). Support new product development with quality compliance. Train teams on quality standards and practices. Ensure supplier quality and address defects. Maintain SOPs, audit logs, and improvement records. Qualifications: Bachelors in Engineering/Metallurgy/Jewellery Tech/Science (MBA preferred). 58 years of QA/QC experience in manufacturing; jewellery industry preferred. 23 years in team leadership and audit coordination. Skills: ISO 9001, jewellery quality inspection, CAPA, QMS/ERP systems. Strong communication, problem-solving, decision-making, and team collaboration.

Job Summary: We are seeking a highly experienced and skilled Deputy General Manager (DGM) Design to lead and manage the design and development of valves and related components. The ideal candidate should possess a strong background in mechanical or metallurgical engineering with hands-on experience in various types of industrial valves. This role involves driving product design, tooling strategies, process improvements, and quality documentation in alignment with ISO standards. Key Responsibilities: Lead the design and development of valves such as gate valves, butterfly valves, swing check valves, and air valves. Develop and approve valve prototypes/samples in coordination with cross-functional teams. Oversee tool design and implement optimized tool manufacturing methods . Maintain and control technical drawings , ensuring alignment with project and customer requirements. Drive compliance and maintenance of ISO documentation , standards, and audits. Provide technical support to production, quality, and sales teams when needed. Coordinate with vendors and customers for design validations and approvals. Mentor and guide junior design engineers to improve team capability. Required Qualifications: Education: B.E./B.Tech in Mechanical or Metallurgy Engineering. Experience: 10 to 15 years of relevant industry experience, with significant exposure to valve design and development. Preferred Expertise: Proven hands-on experience in gate valves, butterfly valves, swing check valves, and air valves. Key Skills: Strong understanding of valve design standards and manufacturing processes Proficiency in CAD software (e.g., AutoCAD, SolidWorks, Creo) Knowledge of tooling techniques , materials, and DFMEA Familiarity with ISO standards and documentation control Excellent problem-solving and leadership abilities Effective communication and project management skills

Knowledge of ISO/IATF standards and documentation Strong coordination and communication skills Hands-on experience with ERP/MIS systems Good analytical and problem-solving skills Drive continual improvement culture across departments.

???? Hiring Now Document Controller | Saudi Arabia ???? *???? Position: Document Controller* *???? Location: Saudi Arabia* * ???? Experience: Min. 5 Years* * ???? Salary: SAR 1500 2000 (?35,000 ?45,500 INR)* *???? Job Summary:* We're looking for a detail-oriented and experienced Document Controller to handle, manage, and organize project documentation. You'll work with systems like DMS / SharePoint and ensure compliance with ISO standards throughout the document lifecycle. *? Key Requirements:* ???? 5+ years of experience in Document Control ???? Proficient in DMS / SharePoint ???? Knowledge of ISO documentation procedures ???? Excellent organizational & communication skills *???? Benefits Include:* ???? Accommodation ???? Transportation ???? Medical Insurance ????? Food Allowance (instead of meals)

NDT - ASNT / ISNT- LEVEL II / III with valid certificates Exp. in Pressure Vessels, Heat Exchangers, boilers & components, manufacturing processes related to fabrication, welding control, heat treatment, inspection, testing, preservation, packing