427 Qms Implementation Jobs

The Quality Management System (QMS) Manager is responsible for developing, implementing, and maintaining the companys quality management system in compliance with industry standards and regulatory requirements Certification needed : ISO Audit Certificate Industry required : Paint/ Chemical/ Automobile Role & responsibilities : Develop, implement, and maintain the Quality Management System (QMS) in accordance with ISO 9001 or other relevant standards. Conduct regular internal audits and coordinate external audits to ensure compliance with regulatory and certification requirements. Identify areas for process improvements and lead initiatives to enhance quality, efficiency, and customer satisfaction. Collaborate with cross-functional teams to ensure quality objectives are integrated into all operational processes. Monitor key quality performance indicators (KPIs) and prepare reports for senior management. Preferred candidate profile : Strong knowledge of ISO 9001 standards and other relevant regulatory frameworks. Excellent analytical, problem-solving, and communication skills. Experience conducting audits and managing CAPA processes. Ability to lead cross-functional teams and drive continuous improvement initiatives. Proficiency in quality management software and MS Office tools.

Our client is a leading provider of innovative solutions across industries like Oil & Gas, Industrial, Defence, Marine, Construction, Energy, Data Centre, Technology etc. With a strong global footprint, they are committed to delivering high-quality products and services while ensuring strict compliance with ISO standards. ISO & Quality Compliance Specialist (based in Peenya Industrial Area, Bengaluru) Overview: Our client is seeking an experienced professional to manage ISO 9001:2015 and ISO 14001:2015 requirements, lead internal audits, maintain compliance documentation, and support continuous improvement initiatives. This position also provides operational and supply chain backup support when needed. Your Responsibilities: ISO & Compliance : Act as lead representative during ISO 9001:2015 and ISO 14001:2015 audits (internal & external). Maintain, review, and update Quality & Environmental Management System (QMS/EMS) documentation. Conduct internal audits, track NCRs, and manage CAPA processes. Train employees on ISO procedures, work instructions, and compliance requirements. Drive continuous improvement initiatives across departments. Customer Quality Assurance: Handle customer quality documentation and promptly respond to quality-related queries. Lead investigations for customer complaints in coordination with HQ and the Sales Team. Manage customer-specific quality records, root cause analysis, and corrective actions. Sales & Operations Support: Assist sales teams with quality and compliance documentation for tenders and proposals. Provide compliance data for customer presentations and audits. Coordinate with operations to ensure fulfilment of customer quality requirements. Operations & Supply Chain : Adhoc support in assembly scheduling, vendor coordination, and logistics tracking. Assist with procurement follow-ups, inventory checks, and stock reconciliation. Your Profile: Diploma or Bachelors degree in Engineering or equivalent. 3 to 6 years in Quality Assurance, Compliance, or QA/QC roles with strong ISO audit exposure. ISO 9001:2015 Internal Auditor Certification is mandatory. ISO 14001:2015 or IMS Auditor Certification is preferred. Familiarity with document control, NCR/CAPA processes, and operational workflows. Candidates from commercial trading of industrial/mechanical products, equipment suppliers, manufacturing, Oil and Gas, EPC services, or engineering services are preferred. Applicants from automotive components, electronics, or similar sectors with transferable ISO skills will also be considered. Strong documentation and record-keeping skills, excellent communication and interpersonal abilities to interact with auditors, customers, and cross-functional teams. A team player interested in working in a collaborative environment. Process-oriented mindset with problem-solving capability. Proficiency in MS Office and ERP systems. Our Offer: Join an international company. A supportive work environment with a focus on teamwork and safety. Competitive salary based on experience. If you are interested in the opportunity, we encourage you to apply with an updated resume. Our consultant will be in touch if your profile meets the specific requirement of our client. Comaea Consulting www.comaeaconsulting.com

Location: Chennai, Tamil Nadu, India Job ID: R0104338 Date Posted: 2025-09-01 Company Name: HITACHI ENERGY TECHNOLOGY SERVICES PRIVATE LIMITED Profession (Job Category): Sales, Marketing & Product Management Job Schedule: Full time Remote: No Job Description: The opportunity Manage a team of Tender Quotation Specialists to deliver high quality, competitive offers and timely submissions to Customers. Prepare Bids & proposals during tendering phase. Drive the team to have complete responsibility for the tenders prepared from IN Operation Center with appropriate inputs from the different stakeholders. How you ll make an impact Lead a team of Tender Quotation Specialists in the preparation of competitive offers. Responsible for process, tool & QMS implementation actions within the team. Implement LOM Tendering process in-line with the global framework. Ensure tendering processes are followed within the team and ensure close, efficient collaboration with all the tendering stakeholders Forecast planning of tenders for the team in close coordination with OU Tendering Managers Take responsibility for team organization, planning, staffing as well as budgeting Resource planning for the new tenders & monitor of the pipeline tenders collaborating with Operating Units Responsible for maintaining internal & external KPIs. Takes responsibility for Tender delivery of the team and ensure KPIs on track. Review & Guide the team members on Tender Solution Strategy in-line with the local market. Guide Analyzing the risk probability & severity of the tenders from technical, commercial, contractual perspectives & support the team towards the mitigation strategy liasing with the different disciplines. Handling of Performance & development for team members and support performance management in-line with the required tendering competencies. Provide feedback to the team members and develop their competency level Identify improvement areas & implement within the team. Training & Development of team members. Handling the daily operational issues and others . Responsible for daily/weekly follow up meetings with the team members . Responsible to ensure compliance with applicable external and internal regulations, procedures, and guidelines. Living Hitachi Energy s core values of safety and integrity, which means taking responsibility for your own actions while caring for your colleagues and the business. Your background Bachelors in Electrical & Electronics with 10+ years of experience in similar role. Masters in Power Systems with 8+ years experience in similar role. Experience in People Management and handling a small team, Deep knowledge in substation tendering and project engineering activities (technical & commercial). Knowledge of Hitachi Energy Products & System offerings). Experience and skill to prepare and support Bid Process. Strong communication and people skills with high focus on internal and external Stakeholders and their needs. Eagerness for learning and innovation, readiness of mind for the use of various new tools for the engineering tasks but also for organizing the team efficiently. Proficiency in both spoken & written English language is required. Qualified individuals with a disability may request a reasonable accommodation if you are unable or limited in your ability to use or access the Hitachi Energy career site as a result of your disability. You may request reasonable accommodations by completing a general inquiry form on our website. Please include your contact information and specific details about your required accommodation to support you during the job application process. This is solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes will not receive a response.

Responsibilities: * Conduct quality audits * Ensure compliance with QMS standards * Implement QMS processes * Manage customer quality expectations * Ensure process control and improvement

They play a key role in implementing and maintaining quality standards, driving continuous improvement initiatives, and resolving complex quality issues to meet the stringent requirements of the automotive industry and its customers

Responsibilities: * Develop ISO Documentation * Should be profecient in Words and excel * Should be able to conduct internal audits * Manage ISMS program * Maintain compliance records * Ensure QMS adherence Travel allowance

Maintain and update QMS docs, lead audits, conduct QC checks, manage CAPA and supplier records, support training, ensure ISO 13485 compliance, and promote quality awareness. Diploma/Bachelor’s with 4–5 yrs in quality/manufacturing preferred.

Support production activities by maintaining and updating production records, performing in-process checks, ensuring compliance with ISO 13485, assisting in equipment and process validations, and supporting proper documentation and record retention.

SOP & STP. Documentation, & reports. Stability Protocol & Compilation of Data. Change control, CAPA initiation, & review. Deviation initiation & investigation. Records of Batch Manufacturing & Packing. Testing WFI, RW & RM. Batch release, QA records. Provident fund

Having exp in handling of QMS implementation in Woven garmenting factories and good exp in Technical and internal audit activities are mandatory. Candidates who completed the ISO9001:2015 QMS Certified auditor training will be additional advantage Required Candidate profile Candidate who has completed the Quality related course or certified from BV/ INTERTEK preferred. For Muzaffarpur Opening, accommodation will be provided. Location: Bangalore & Muzaffarpur Factories.

Having exp in handling of QMS implementation in Woven garmenting factories and good exp in Technical and internal audit activities are mandatory. Candidates who completed the ISO9001:2015 QMS Certified auditor training will be additional advantage Required Candidate profile Candidate who has completed the Quality related course or certified from BV/ INTERTEK preferred. For Muzaffarpur Opening, accommodation will be provided. Location: Bangalore & Muzaffarpur Factories.

Lead testing & inspection teams for raw materials & finished product Develop & implement quality assurance programs Identify & resolve quality issues Conduct audits Collaborate with teams to optimize quality processes Drive cost-effective solutions

Hands on experience with PLEX Supplier Quality and Manufacturing Quality PLEX MES Module PLEX CMMS Module PLEX A&O Module (Automation and Orchestration) PLEX APM Module (Asset Performance Management) PLEX PM Module (Production Monitoring)

Set & maintain quality policy. Integrate QMS into processes. Provide necessary QMS resources. Lead support participation QMS. Meet customer legal requirements. Identify address risks and opportunities. Assign QMS roles, reporting, change management.

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 clients QMS and quality training requirements. Responsible for ensuring that the work conducted by the Facilities team, and its subcontractors is in full compliance with contractual requirements, clients SOPs, GxP, FDA and other regulations. Able to perform/support internal JLL compliance audits and prepare SOPs, and training materials for use by the Life Sciences facilities team in the performance of their work. Guide Life Sciences facilities team in closing recommendations from clients audit. Expected to interface with the clients quality personnel to ensure that all of the clients SOPs are followed, work performed by the LS facilities team is properly documented for traceability in the framework of GDP. Sustain quality assurance support and develop a Quality Engineering Maintenance program for a controlled-environment manufacturing and laboratory facility as it relates to the facilities maintenance of this plant. Conduct investigations and drive accountability for all quality events. Lead programs to create value for client to ensure program deliveries meet or exceed expectations. Facilitate quality-relevance investigation via structured Root Cause Analysis. As part of career development, lead Life Sciences accounts as an IFM leader.Reporting Manage and report on critical & key performance measurements. Develop and submit periodic site status reports related to the Quality Program. People Management Effectively lead and guide a Life Sciences Quality team by clearly communicating expectations, accountabilities and providing performance feedback for continuous improvement. Ensure Life Sciences Operations team members complete relevant quality and compliance training. Coach new Life Sciences team members on quality and compliance for their adaptation into specific Life Sciences accounts. Mentor, develop and train peer and direct report team members. Provides direction/information to vendors, facilities staff and service providers as required to ensure that quality assurance expectations are communicated and followed.Others Any other quality-relevant duties and tasks assigned. Knowledge, Skills & AbilitiesMINIMUM REQUIRED PREFERRED Education/training Bachelor degree preferred Degree in science, technical or relevant discipline Sound fundamental knowledge in process utilities. 6+ Years of relevant experience preferred with minimum 4+ years in Quality and Compliance discipline in GxP manufacturing or laboratory environment. Six-Sigma and Root Cause Analysis training is essential.Skills and knowledge Background in technical documentation Work independently and within a team. Strong mindset of compliance and client-focus. Communicate effectively with technical, quality assurance and other personnel. Proficient in Word, Excel and other Microsoft Office Suite programs Ability to investigate, recognize and diagnose trends and patterns. Solid understanding of cGMPs as they relate to the performance of maintenance and repairs to facilities, utilities and equipment utilized for the manufacturing plants and laboratories for drug products. Experience working at an FDA regulated manufacturing facility in a quality assurance or quality control capacity. Support investigations and corrective action plans for appropriate discrepancies. Investigation of compliance issues as required, collaborating with relevant Compliance Partner(s) Understanding of FDA regulations including 210 CFR part 210 and 211. Strong commitment to quality assurance, and a willingness to help develop a quality first culture on the site. Knowledge of Quality Engineering techniques, CMMS systems, and Quality Management Systems English communication is essentialOther abilities Good oral and written communication skills including the ability to communicate to all levels of management and willing to interface with a diverse customer base including technical and non-technical personnel.Physical work requirements and work conditions Familiar with process utilities and GxP environment.On-site Aurangabad, MH

Focus on ISO STANDARDS & IMPLEMENTATION, CUSTOMER HANDLING, DATA ANALYSIS, APQP, PPAP, FMEA, SPC, SIX SIGMA, RISK ASSESSMENT, ROOT CAUSE ANALYSIS, QMS DOCUMENTATION, QMS IMPLEMENTATION, QUALITY SYSTEM AUDITS, QMS AUDIT, QA CERTIFICATIONS, CQA etc Required Candidate profile DIP/BE 6+yrs exp into QA Strong exp with Greenfield plants & EMS unit preferred Exp in handling ISO IMPLEMENTTION, SIX SIGMA, OEM CLIENT SUPPORT, APQP, PPAP, FMEA, SPC, QMS AUDITS et Call @ 9677076683 Perks and benefits Excellent Perks. Send CV to cv.ch1@adonisstaff.in

At TE, you have the opportunity to work with diverse backgrounds and industries to contribute to creating a safer, sustainable, and more connected world. **Key Responsibilities:** - Collaborate with vendors, communicate requirements, manage purchases, and ensure quality standards are maintained. - Estimate timelines, determine specifications and related costs, oversee inspections, and drive quality improvement. - Assist in implementing quality plans, programs, and procedures using quality control statistics and lean manufacturing concepts. **Qualifications Required:** - BE/ B.Tech (Electronic, Mechanical) degree - Six Sigma Green/Black Belt certification preferred - Knowledge of Quality Core Tools - Certified Internal Auditor for IATF & VDA 6.3 **About TE Connectivity:** TE Connectivity plc (NYSE: TEL) is a global industrial technology leader focused on creating a safer, sustainable, and connected future. With a diverse range of connectivity and sensor solutions, TE enables advancements in transportation, energy networks, automated factories, data centers, medical technology, and more. TE Connectivity Offers: - Competitive Salary Package - Performance-Based Bonus Plans - Health and Wellness Incentives - Employee Stock Purchase Program - Community Outreach Programs/Charity Events - Employee Resource Group **Additional Company Information:** TE Connectivity ensures that every connection counts by working closely with customers in approximately 130 countries. The company has over 85,000 employees, including 9,000 engineers, dedicated to creating a better future through innovative solutions. **Competencies:** - Values: Integrity, Accountability, Inclusion, Innovation, Teamwork **Critical Experience:** - Strong knowledge of IATF 16949, ISO 9001, VDA 6.3, and CQI standards. - Understanding of APQP, PPAP, MSA, SPC, FMEA, Control Plan, 8D. - Excellent problem-solving and analytical skills. - Strong documentation and process orientation. - Effective communication and stakeholder management skills. - Experience in handling customer audits and OEM requirements.,

SMT Quality Engineer with focus on QMS & audits. Ensure IPC-standard compliance, lead internal & external audits, monitor SMT process quality, drive CAPA, and support certifications. Strong knowledge of ISO standards & QMS systems essential.

We are seeking a skilled QMS Consultant. This role is critical in helping automotive manufacturers and suppliers adhere to IATF 16949, CQI ,Lean Sixsigma , GD&T , ISO 14001,ISO 45001,VDA standards by developing and implementing effective QMS Measures

We are seeking a skilled QMS Consultant. This role is critical in helping automotive manufacturers and suppliers adhere to IATF 16949, CQI ,Lean Sixsigma , GD&T , ISO 14001,ISO 45001,VDA standards by developing and implementing effective QMS Measures

Quality Management System Defect Analysis New Product Execution Core Tool Implementation Supplier Development VW, BIQS, Toyota, MSIL, Fiat customer requirements Program / Project Manager

Job Title : Quality Manager (Trained ISO/IEC 17025) Location : Faridabad Job Summary : We are seeking a highly skilled and experienced Quality Manager to oversee the quality management system in the laboratory. The ideal candidate will have experience in carrying out NABL (National Accreditation Board for Testing and Calibration Laboratories) audits as per ISO/IEC 17025 and a strong understanding of laboratory quality Management processes. The Quality Manager will play a key role in ensuring the laboratory's operations meet national and international standards of quality, accuracy, and reliability. Key Responsibilities : Develop, implement, and maintain the laboratorys Quality Management System (QMS) as per the ISO/IEC 17025 and NABL guidelines. Lead and coordinate the NABL audits (internal and external), ensuring compliance with all relevant standards. Monitor and ensure compliance with laboratory policies, procedures, and regulatory requirements. Identify and address quality issues within the laboratory, implementing corrective and preventive actions as needed. Prepare, review, and maintain the documentation for the laboratory's quality management system, including audit reports, corrective actions, and risk assessments. Ensure the laboratorys equipment and facilities are properly calibrated and maintained to meet required standards. Collaborate with other departments and stakeholders to promote a culture of quality within the organization. Continuously evaluate and recommend improvements to the laboratory's processes and systems to enhance quality and operational efficiency. Stay updated with changes in quality standards, regulations, and best practices, ensuring the laboratory stays in compliance with industry standards. Qualifications & Requirements : Educational Qualification : Minimum B.Sc degree Or M.Sc. Experience : Minimum of 5 years of experience in laboratory quality management, including experience in conducting NABL audits as per ISO/IEC 17025 . 4 days Intenal Quality Management Training on ISO/IEC 17025:2027 Strong understanding of laboratory accreditation standards, quality assurance practices, and continuous improvement techniques. In-depth knowledge of ISO/IEC 17025 and NABL accreditation processes. Proven experience in preparing for and managing successful audits, both internal and external. Strong analytical skills, attention to detail, and the ability to troubleshoot complex quality issues. Excellent communication, organizational, and interpersonal skills. Ability to work independently and as part of a team, managing multiple tasks and projects.

RESPONSIBILITIES: 1. Quality Leadership & Compliance Lead the Quality Assurance department and ensure compliance with GMP, regulatory guidelines, and company policies. Implement, monitor, and continuously improve quality systems across the organization. Oversee documentation control and ensure data integrity in all QA processes. 2. Quality Oversight & Decision-Making Oversee and approve critical quality documents (such as master SOPs, batch release records, change controls, deviations, and CAPA) while ensuring effective review by the QA team. Ensure timely closure of investigations related to deviations, OOS, and complaints, with effective corrective and preventive actions. Authorize batch release in line with regulatory and company requirements. Ensure qualification and validation of equipment, utilities, and manufacturing processes as per regulatory expectations. 3. Audits & Regulatory Inspections Conduct internal audits and ensure site readiness for external audits (regulatory and customer). Act as the primary point of contact during inspections by regulatory authorities and clients. 4. Team Management & Development Guide, train, and develop the QA team to strengthen compliance and quality culture. Allocate responsibilities within the QA department and monitor performance. 5. Cross-Functional Collaboration Collaborate with Production, QC, Engineering, and other departments to resolve quality-related issues. 6. Continuous Improvement Drive initiatives across the plant to enhance quality systems, compliance, and overall quality culture. REQUIRED SKILLS AND KNOWLEDGE: Bachelors/Masters degree in Pharmacy, Chemistry, or related field. Minimum 13+ years of experience in Quality Assurance, with at least 5 years in a leadership role in the pharmaceutical industry (API) . Strong knowledge of GMP, ICH, WHO, USFDA, MHRA, and other regulatory guidelines . Proven experience in facing regulatory inspections and handling audits . Expertise in change control, deviation, CAPA, OOS investigations, and batch release . Excellent leadership and people management skills. Strong documentation control and data integrity orientation . Good communication skills with proficiency in English (written and spoken). Knowledge of Telugu and Hindi preferred for better coordination with cross-functional teams. HOW TO APPLY: Email resume to prasant.vadada@metroapi.com (subject: Application - QA Head - Kazipally/Bonthapally). Talent Acquisition team will screen resumes and contact shortlisted candidates for an initial interview via telephonic. Candidates shortlisted after the initial round will be scheduled for further interviews with the Corporate QA Head, Plant Head, and/or Management (if required) Please carry original ID and educational/professional documents when called for in-person interview. Note: For any information before applying, or to track your application/recruitment status, you may contact Mr. V. Prasant (HR) at 8637085495 / 9679617228 .

ROLE OBJECTIVE To ensure effective implementation and continual improvement of the Quality Management System in line with IATF 16949, ISO 9001, VDA standards, customer-specific requirements, and organizational goals. KEY RESPONSIBILITIES Quality Management System Implementation Ensure effective implementation and compliance of QMS across the organization. Drive alignment with IATF 16949, ISO 9001, VDA 6.3, and customer-specific requirements. Develop, update, and monitor QMS documents including Quality Manual, Procedures, Work Instructions, and Records. Conduct gap analysis and initiate corrective & preventive actions. Audits & Compliance Plan, conduct, and support internal audits, process audits, product audits, & layered process audits Facilitate external/customer audits and ensure timely closure of NCs. Ensure calibration, MSA, and traceability compliance. Training & Awareness Create training plans and provide QMS awareness to employees. Build knowledge about quality systems across all teams. Document & Change Control Manage document control and revision updates. Manage and coordinate engineering and process change controls at site level. Quality Improvement & Risk Management Drive continuous improvement projects in line with TEOA / Lean / Six Sigma initiatives. Support risk management activities through PFMEA, DFMEA, and robust process controls. Customer & Stakeholder Management Support customer requirements related to QMS compliance. Ensure customer complaints, feedback, and audit findings are addressed effectively. Prepare QMS-related reports and present to Plant leadership. Track KPIs such as COPQ, audit closure rates, customer complaints, and process adherence. EDUCATION/KNOWLEDGE BE/ B.Tech (Electronic, Mechanical) Six Sigma Green/Black Belt preferred Knowledge of Quality Core Tools Should be Certified Internal Auditor for IATF & VDA 6.3 CRITICAL EXPERIENCE Strong knowledge of IATF 16949, ISO 9001, VDA 6.3, and CQI standards. Good understanding of APQP, PPAP, MSA, SPC, FMEA, Control Plan, 8D. Excellent problem-solving and analytical skills. Strong documentation and process orientation. Effective communication and stakeholder management skills. Experience in handling customer audits and OEM requirements. COMPETENCIES Strong understanding of QMS standards (IATF 16949, ISO 9001, VDA 6.3). Knowledge of customer-specific requirements. Awareness of risk-based thinking and continuous improvement methods. Ability to plan, conduct, and report audits independently. Skilled in identifying non-conformities and root causes. Ability to check effectiveness of corrective and preventive actions. Strong Communication Skills Clear reporting and explaining findings. Influencing Skills Should be able to guide teams to accept and act on improvements

Vacancy for QMS Engineer in Sheet Metal Industry Exp - 3 to 5 years IATF 16949:2016, Internal Auditing, QMS, MR Responsibilities IATF/EHS Qualification - BE / Diploma Mechanical Location - Chakan Pune. On Roll Job Call on - 8408824722/ 9518340393