383 Iso Documentation Jobs - Page 3

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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 standards, customer specifications, and regulatory requirements. Maintain documentation such as quality manuals, procedures, inspection reports, and non-conformance records.

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 track KPIs for core and support processes; drive gap analysis and improvements. Oversee application of APQP, PPAP, FMEA, MSA, and SPC in relevant functions; support teams in correct and effective usage. Drive structured change control process for product, process, and system-level changes. Ensure deployment and compliance of Customer-Specific Requirements (CSR) within the QMS. Establish and monitor risk analysis and contingency planning for business continuity. Develop and deliver QMS training; build awareness across functions on quality standards and updates. Drive, Train & Facilitate QC & production for QC circle teams to resolve perennial issues. Localization : Responsible for establishing Quality of parts developed as per management initiatives. Support supplier for understanding current supplier product quality and guide in establishing a similar or supplier quality products. Support in completion of testing and validations of parts as per all applicable engineering standards and facilitate for customer approval as per the requirements stated by customer. Qualifications: Mandatory: B.E./ B.Tech Mechanical Desired: IATF / VDA certification Functional/Technical Competencies Required: IATF 16949, VDA 6.x, APQP, PPAP, FMEA, MSA, SPC, Control plan, VA/VE, Benchmarking, Customer management, Problem solving techniques, 8D approach, MS Office. Behavioural Competencies Required: Stake holder management, Communication, Leadership, Agile mindset, People management, Customer management, Supplier management, Self initiative & Proactive, Process driven approach. Key result areas / job outcomes: Drive and achieve QMS certifications by effective implementation of QMS Completion of internal system audit plan No of QCC projects completed Customer specific QMS implementation & rating / ranking as per customer systems % of parts localised as per management target Interested Candidates can send their CV on alka.p@peoplesource.in. Immediate joiners will be preferred. Alka Pathak Tiwari Senior Recruitment Consultant Email: alka.p@peoplesource.in

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). - Managing and implementing change control processes effectively. - Proficient in preparing and maintaining Site Master Files, Master Validation Plans, and Batch Manufacturing Records (BMRs). - Conducting stability studies, managing stability programs, and handling Out of Trend (OOT) and Out of Specification (OOS) results. - Establishing and maintaining standards according to current regulatory guidelines and Pharmacopeia revisions. - Evaluating deviations, managing change controls, and implementing corrective and preventive actions (CAPA). - Proficient in equipment qualification, process validation, cleaning validation, and method validation. - Overseeing the calibration of equipment and adhering to ICHQ7A guidelines and other regulatory standards. - Conducting trend analysis, providing feedback for continuous improvement, and implementing Quality Risk Management strategies. - Working towards continuous improvement of quality systems and efficiently managing Quality Control departments. - Handling ISO documentation procedures, including quality manuals, work instructions, checklists, and audits. - Managing sampling and testing of excipients, Essential Oils, and Aroma chemicals. - Strong skills in effective manpower handling and communication in English, both oral and written. This is a full-time position with benefits including Provident Fund. The work schedule is day shift, and the work location is in person.,

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 material checked by IQC during receiving of material. 7. Creating Quality awareness by conducting training for Executive/ Supervisors whose work will affect the Quality of the product. 8. Responsible for implementation of standards related to quality at supplier and verification of implemented standard through the audit at supplier. 9. Responsible for approval of material made under 4M Change and abnormal situation. 10. Responsible for submission of countermeasure against customer complaints. Preferred candidate profile QMS Engineer Perks and benefits

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 Internal & External Audits and ensure that the non-conformities are closed in a time bound manner. Compliance Management Responsible to identify and implement the compliance requirements pertaining to Environment, Occupational Health and Safety for site locations and perform compliance submissions to various authorities in time bound manner. Responsible maintain compliance requirement for sites for applicable compliance conditions in EHS domain. Responsible to Coordinate government bodies like SPCB, CPCB, DISH etc. during their site visits. ESG (Sustainability) Reporting Collect and submit the data required for ESG reporting to relevant stakeholders within the organization. EHS Accountabilities Responsible for coordination to obtain EHS related licenses and permissions from various government bodies. Responsible to identify EHS requirements for the project components during expansion or modification, and proactively communicate with relevant stakeholders to ensure its implementation. Suggest to use the technologies which are in line with Sustainability Goals of the organization. EHS Performance improvement of Site location Review the EHS performance of the site by participating a EHS Review meeting with Management and ensure the requirements are fulfilled for various EHS related activities. Responsible to execute strategies for implementation of work practices which improves EHS performance of the organization. Perform investigations for Incident or Accidents as per common procedure and ensure that the corrective actions are implemented to align with the organizational goal of Zero Incident. Training and awareness Responsible to design training contents for EHS related Topics and impart relevant training to implement EHS management system. Celebrate various EHS related important days to improve awareness among the employees. Knowledge, Experience and SkillsQualification M.Sc./ B.Sc. Fire; or B.E./B.Tech/M.Sc. Environmental Science or relevant domain of Environment, Health and Safety; or equivalent Post Diploma in Industrial Safety or equivalent (Mandatory) Experience 6 to 8 years of experience in EHS Department SkillsSkill AreaLevel or depth requiredPurpose Collaboration and coordinationHigh level of competency requiredTo establish EHS culture for organization.To perform various IMS related documentation done through various stakeholders.Decision MakingHigh level of competency requiredTo guide the organization in various compliance requirements during project phase as well as during operational phase.Meeting EffectivenessModerate competency requiredTo communicate cross functional EHS activities and implement EHS requirementsConflict ManagementModerate competency requiredTo resolve cross functional conflicts generated due to cross functional EHS requirements.Collaboration and coordinationHigh level of competency requiredTo establish EHS culture for organization.To perform various IMS related documentation done through various stakeholders.

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 us to deliver components with consistent accuracy, even at nano-levels. From connector pins and contact terminals to sensor housings and relay parts , each component is engineered with a focus on dimensional stability, material integrity, and functional reliability . Our production environment adheres to cleanroom standards , supported by in-line vision systems and rigorous quality protocols, ensuring zero-defect delivery. Position Summary: The Vice President Quality will lead and shape Company's global quality strategy from its India hub. You will oversee quality systems, compliance, and continuous improvement initiatives across multiple manufacturing lines, ensuring alignment with international standards (ISO, IATF, etc.) and customer expectations in the consumer electronics and High precision component sectors. Key Responsibilities: Strategic Quality Leadership: Define and execute a comprehensive quality vision and roadmap aligned with corporate goals. Lead the organization toward zero-defect manufacturing and world-class quality systems. Quality Systems Management: Oversee implementation, maintenance, and improvement of ISO 9001, IATF 16949, ISO 14001, and other relevant standards. Ensure compliance with customer-specific requirements and regulatory standards. Operational Excellence: Establish robust in-process quality controls, end-of-line testing, and root cause analysis mechanisms. Drive Six Sigma, Lean Manufacturing, and continuous improvement across quality operations. Customer Engagement: Act as the primary quality interface for key global customers and regulatory bodies. Lead audits, manage customer complaints, and implement corrective/preventive actions (CAPA). Team Development: Lead, mentor, and grow a high-performing, multi-disciplinary quality team. Foster a culture of ownership, accountability, and proactive problem-solving. Cross-functional Leadership: Collaborate with R&D, Engineering, Manufacturing, and Supply Chain to embed quality into design and production. Provide input on supplier quality and global sourcing strategies. Qualifications: Bachelors or Masters degree in Engineering or related technical discipline. 18 to 24 years of progressive experience in Quality, with at least 5 years in a senior leadership role in a precision manufacturing or electronics environment. Deep understanding of ISO, IATF, IPC standards, and global regulatory requirements. Proven success in building and leading large quality teams across sites or regions. Strong customer-facing communication, audit readiness, and project management skills. Six Sigma Black Belt or equivalent certification is preferred. What We Offer: A leadership role in a fast-scaling, global manufacturing company. Opportunity to shape and institutionalize quality excellence in a greenfield/expanding facility. Competitive compensation, benefits, and professional development opportunities. Collaborative and innovative work culture with global exposure. Apply Now Thanks and Regards L Sainath Jayaram SAI HR CONSULTANTS DIRECTOR TALENT ACQUISITION 8015088704 sainathjayaram95@gmail.com

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 documentation such as policies, procedures, manuals, and audit reports. Advise clients on compliance strategies and continuous improvement. Deliver training and awareness sessions to client teams. Coordinate with certification bodies and assist during third-party audits. Ensure timely project delivery and client satisfaction. Keep up to date with changes in ISO standards and regulatory requirements. Requirements: Bachelors degree in Engineering, Environmental Science, IT, or a related field. Minimum 8 years of relevant experience in ISO consultancy or auditing. Certified Lead Auditor in ISO 9001, 14001, 45001 (mandatory). Lead Auditor certification in ISO 27001 and 37001 (preferred or willing to obtain). Strong knowledge of management system integration. Excellent communication, project management, and analytical skills. Ability to work independently and manage multiple client engagements. Willingness to travel as required. Preferred Qualifications: Experience working under ISO/IEC 17021 framework. Knowledge of local and international compliance requirements. Previous experience with certification bodies or third-party audits.

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

Our Esteemed client in Isolation valve industry in Pune is looking for Assistant Manager QA with relevant experience of 8 to 12 years in Inward, In process and Final Quality. Required Candidate profile University Engineering Degree in Mechanical, Production or Instrumentation is required. Atleast 4-5 years of experience with Isolation valves or similar industry is mandatory.

Acquire prospective customer from food & agri industries for business. End-to-end handling of QMS, FSMS, ISO & other systems certification for the customers which includes training, documentation, implementation & audits of prospective clients. Required Candidate profile B.Tech/M.Tech in Food Science with experience in FSMS/QMS/ISO implementation and documentation

Female candidates as Process Consultant, Chennai office (Mon to Sat) This includes tasks like conducting risk assessments, Develop security policies, Compliance, Security Incidents etc Establishing and Maintaining the ISMS/QMS and other standards Required Candidate profile 2 years of experience in information security Basics of ISO standards, frameworks, cloud infrastructure and security CMMI documentation (CMMI framework, QMS, ISO, Process mapping, CMMI) 9884000283

Manage the HDPE,OPVC pipe, Fitting production factory including production activities, Raw Materials planning and Manpower. Supervise effective maintenance of all machines. Manage a team of more than 100 people. Manage over all plant activities. Required Candidate profile Experience in HDPE/OPVC Pipe Industry is essential Taking care of overall production activities Resource management and achievement of Target Integrated Management system, documentation and compliance

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 execution and documentation. Evaluate the effectiveness of Quality Management Systems using a process-based, risk-driven approach. Review and assess compliance with railway-specific requirements, including operational and regulatory standards. Identify, document, and classify non-conformities; support the implementation of corrective and preventive actions (CAPA). Deliver clear and concise audit findings and reports to relevant stakeholders. Monitor follow-up actions to ensure timely closure of audit issues and drive continuous improvement. Liaise with external auditors and support third-party IRIS certification or surveillance audits. Train and guide internal teams on IRIS requirements, audit readiness, and QMS best practices. Analyze IRIS performance levels and contribute to achieving higher ratings (e.g., Silver, Gold). Keep updated with industry changes, IRIS portal updates, and evolving regulatory requirements. Required Qualifications & Skills: Bachelor's degree in Engineering, Quality, Industrial Management, or related field. Minimum [X] years of experience in Quality Management or IRIS auditing within the railway or industrial manufacturing sector. Strong knowledge of ISO 9001 and ISO 22163 (IRIS Standard). Proven experience in conducting IRIS audits , including audit planning, execution, and reporting. Proficiency with audit techniques such as interviewing, observation, and document review. Familiarity with the IRIS Audit Tool and IRIS Portal usage. Experience in non-conformance management and CAPA processes . Strong communication, interpersonal, and presentation skills. Ability to work independently and collaboratively across cross-functional teams. Detail-oriented mindset with a commitment to continuous improvement . Preferred Certifications: Certified ISO 9001 Lead Auditor or equivalent. IRIS Auditor Certification (if applicable or preferred). Six Sigma or Lean certification (optional but beneficial).

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 responses to audit findings. Non-Conformance Management: Identifying, investigating, and resolving non-conformities, implementing corrective and preventative actions (CAPA). Customer Complaints: Managing customer complaints, conducting root cause analysis, and implementing preventive measures.

JOB PROFILE: Overall responsibility of electrical maintenance department related activities inside and outside the plant. JOB CONTENT: Preventive Maintenance Planning & Scheduling. Trouble shooting Handling a team Ensuring the EHS and environment management system documentation and KPIs pertained to the dept through periodical review. Handling entire Electrical statutory requirements Implementation of Electrical safety management system (LOTOTO, Hand tool safety, Earthing & Bonding, HD yard Maintenance) Hazardous area classification. KEY RESPONSIBILITIES: 1)To plan and execute the maintenance schedule for upkeep of equipment. 2)To maintain control on energy consumption. 3)To attend equipment breakdowns and trouble shoot repeated failures. 4) To comply all the statutory requirements related to Electrical function and to ensure the electrical safety in the Plant. 5) To provide necessary resource for carrying out repairs and maintenance of the equipment including CAPEX. 6) Resource planning and preparation of R&M expenses for the budget and monitoring the expenses and analyzing the R&M expenses and reporting. 7) To provide training to all the team members and co-ordinate training programs with HR department 8) To analyze the performance of the equipment and to study the equipment reliability every month. 9) To lead the team in implementing Quality System initiatives such as 5S & Kaizen. 10) To fulfill the QMS / EMS / OHSAS / GMP requirements. QUALIFICATION: Diploma in Electrical with 4-8yrs of experience. Experience in a pharma, petrochemicals, chemicals, process plant maintenance and utility operations Interested candidates can share their resumes to stk3@sanmargroup.com, Shortlisted peoples need to relocate Hosur / Berigai location - Job location

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

Conduct inspections and examinations of products, processes, to assess their quality and compliance with established standards.Implement quality control procedures and best practices. Maintain detailed records of quality assessments and test results. Required Candidate profile Diploma / BE with 1+ year of experience in Quality department of engineering company. Must have very good experience of documentation, quality management and testing. Job based at Baroda.