428 Qms Implementation Jobs - Page 5

Role & responsibilities To take the lead in implementing & improving Quality Management System across multipal sites. Ensuring compliance with ISO 9001, IATF 16949, ISO 45001 & ISO 14001 Standards Lead system/ internal audits & ensure timely closure of non conformances with a recurrence prevention approach. Coordinate external certification audits by liaising with certification agencies Creating & updating standards based on customer audits and customer specific requirements Continuously review standards for business process improvements Conduct management review meetings Develop & deliver QMS/IMS related training programs across sites Preferred candidate profile Essential: Should have been in corporate lead QMS position for a minimum 08 to 10 years and certified as lead auditor. Have good experience in VDA 6.3 standards Automotive background throughout the career. Prior manufacturing / design experience. Good knowledge of digital tools. Good leadership and communication skills. Desirable: Network with societies like ACMA, CII, TQI, etc.

Job Description We are looking for an experienced and detail-oriented QA Manager to join our team in an Injectable Pharma Plant. The ideal candidate should possess strong knowledge of pharmaceutical quality systems, regulatory compliance, and hands-on exposure to validation activities. Key Responsibilities: Lead QA operations in an Injectable Pharma Plant ensuring compliance with cGMP and regulatory requirements. Handle complete validation activities including Autoclave, DHS, and HVAC validations. Monitor and ensure compliance of Media Fill, Temperature Mapping and other critical processes. Manage QMS activities such as Change Control, Deviations, CAPA and ensure timely closure. Act as the front face during audits/inspections and ensure effective CAPA implementation post audit. Ensure adherence to Good Documentation Practices (GDP) and prepare, review, and update SOPs . Conduct training sessions for employees on new/revised SOPs. Coordinate with Microbiology & QC departments and provide basic technical support. Desired Candidate Profile: Minimum 5 years of experience in QA in an Injectable Pharma Plant. Strong knowledge of QMS, regulatory compliance, and validation activities . Excellent communication and leadership skills. Ability to lead audits and represent the organization effectively. Team-oriented professional with attention to detail. Perks and Benefits: Competitive Salary [Insert Range if applicable] Growth and learning opportunities in a reputed organization Exposure to regulatory audits and international compliance standards

Role & responsibilities Oversee the implementation and maintenance of the Quality Management System (QMS) in line with ISO standards and company policies. Act as the primary point of contact for quality matters between the organization, customers, and regulatory bodies. Investigate and resolve customer complaints in depth , identifying root causes and ensuring effective corrective and preventive actions. Coordinate internal audits, inspections, and compliance checks to ensure adherence to quality standards. Monitor process performance and quality metrics , recommending improvements to enhance product and service quality. Ensure proper documentation of quality records, CAPA (Corrective & Preventive Actions), and NCRs (Non-Conformance Reports). Collaborate with cross-functional teams (production, R&D, supply chain) to implement quality improvement initiatives. Train employees on quality procedures, standards, and best practices to foster a culture of quality awareness. Review and approve quality reports and customer feedback summaries before submission to management or clients. Liaise with customers and vendors to communicate quality expectations, updates, and resolutions effectively. Preferred candidate profile Qualification: B.E / B.Tech / Diploma in Mechanical, Production, Industrial, or related Engineering fields. Min Experience: 10 years in quality management, preferably in manufacturing or engineering industries. Certifications (preferred): ISO 9001 Lead Auditor, Six Sigma, or equivalent quality management certifications. Strong experience in handling customer complaints, root cause analysis, and implementing corrective & preventive actions (CAPA). Knowledge of quality standards, regulatory compliance, and documentation practices . Excellent analytical, problem-solving, and process improvement skills . Strong communication and coordination skills to liaise with customers, vendors, and internal teams. Proactive, detail-oriented, and capable of driving quality initiatives across departments . Familiarity with internal audits, NCR management, and quality reporting tools .

Roles and Responsibilities Handle customer audits, internal process audits, and system audits related to IATF standards. Prepare and review ISO documentation for QMS implementation. Conduct quality management system (QMS) audits according to customer requirements. Ensure compliance with industry regulations and standards through effective QMS practices. Collaborate with cross-functional teams to identify areas for improvement in the organization's processes.

Being a Biotech graduate having one - two - three years experience in biotech manufacturing industries in all department reputed biotech industries required urgently in Vapi and Daman surrounding area. Required Candidate profile BSC Bio / Msc Biotech / B. tech Biotech / Fresher or experience 1 / 2 / 3 years.

POSITI ON:- DGM-GENERAL MANAGER QUALITY CONTROL Work in a challenging position in a quality driven organization to provide professional expertise and service by continuous improvement, learning, growth and technological up gradation and achieve growth. CORE COMPETENCIES : Team work, Problem Solving, Customer Service, Interpersonal Skills, Managing Peoples, Change management, Organizational support, Planning & Organizing, Delegation, Business Acumen, Cost consciousness, Ethics, Professionalism, Adaptability, Safety & Security, Innovation AREAS OF EXPERTIES: Taking care and Ensure all Products Quality which is manufacturing in Nashik Plant. Lead a Team of 30 to 35 Employee / inspectors in the Department Ensure QMS Implementation in each Process / Products all the time. Through Process monitoring and System Implementation ensure Quality Product Manufacturing with minimum Manpower requirements. Well and Advance planning in all Quality activities from Raw material receipt to Finished Goods Dispatch. Ensure Quality / Delivery in all stages On time / EveryTime. Through Past History and Present Quality filter in each supplier Via Vendor Rating Card Feeding Quality Product to production Process lines. Prime Focus on Vendor Development / Contract Manufacturing / Buy Sell Concept Quality / Outsourced product Quality. Should have Rich Experience in Handhold the Vendor to meet our Quality requirements and Find out Right Supplier for Right Products. He should Attend the Kick of Meeting (KOM) and Pre Inspection meeting (PIM) to Customer and understand the Customer Requirements & get the Clarification for various points of Customer Requirements from Customer / EPC (Project Executer) and meets the Requirements Successfully.. Raw Material Inspection Like, Castings ( Body & Bonnet ), Forgins ( Stem, Disc ) & Other Materials, Raw Materials & Finished Valves Offer to Third Party Inspector in Various Stages & Final Inspection Making Quality Assurance Plan (QAP) / Inspection Test Plan ( ITP) & Special requirement Charts. Depends upon the Customer Requirements, Making Quality Assurance Plan and handed over to Sales Co Ordination Department & follow up to the Customer for getting Approval. Third Party inspectors, Expeditors & Customers in both Export & Domestic Project Orders to be Handled. Documents hand over to Third Party Inspectors on time and getting Inspection Release or Shipping Release as soon as possible. Line by Line Status & Activities in Project Orders giving to Expeditor & Customer in right Time. Maintain good relationship with all Third party Inspection Agencys.

About the team: ZF''s Commercial Vehicle Solutions (CVS) division helps shaping the future of commercial transportation ecosystems. Our mission is to be the preferred global technology partner for the commercial vehicle industry. What you can look forward to as Assistant Manager/Senior Engineer: Handling supplier for routine issues and daily NC management.. Handling daily quality issues with supplier and on time closer of issues with CAPA. Closely Working with supplier for process Audits/ improvement to get zero defect. Implementation of ZF DNA principles at supplier end to build quality culture. Prepare, Monitor and maintain supplier report. Coordinate and drive change management with internal and external stake holder Responsible for APQP launch, PPAP and drive new development activity. Responsible for supplier performance/PPM within business target. Your Profile as Assistant Manager/Senior Engineer: Must have experience of Supplier Quality. BE/Diploma in Mechanical/Automobile/Metallurgy, 6 to 10 years of experience. Knowledge of Quality Core Tool, IATF/ISO. Knowledge basic manufacturing process (casting, forging, rubber molding, Coating, Platting, Tube manufacturing, etc.) This position needs to work between ZF & Supplier Knowledge of APQP, PPAP,8D, QRQC.Handling supplier Audits, VDA 6.3 lead Auditor will be added advantage. Why should you choose ZF Group in India? Innovation and Technology Leadership: ZF is at the forefront of technological advancements, offering a dynamic and innovative work environment that encourages creativity and growth Diverse and Inclusive Culture: ZF fosters a diverse and inclusive workplace where all employees are valued and respected, promoting a culture of collaboration and mutual support Career Development: ZF is committed to the professional growth of its employees, offering extensive training programs, career development opportunities, and a clear path for advancement. Global Presence: As a part of a global leader in driveline and chassis technology, ZF provides opportunities to work on international projects and collaborate with teams worldwide. Sustainability Focus: ZF is dedicated to sustainability and environmental responsibility, actively working towards creating eco-friendly solutions and reducing its carbon footprint. Employee Well-being: ZF prioritizes the well-being of its employees, providing comprehensive health and wellness programs, flexible work arrangements, and a supportive work-life balance. Be part of our ZF team as Assistant Manager - Plant Supplier Quality and apply now!

We are seeking an experienced SAP QM Solution Lead / Architect with deep expertise in SAP Quality Management (QM), solution architecture, and S/4HANA. The ideal candidate will have a strong background in managing end to end SAP implementations, leading cross functional teams, and delivering scalable solutions aligned with business goals. Key Responsibilities: Lead the implementation, development, and support of SAP QM solutions on S/4HANA. Analyze and document detailed business requirements and translate them into functional specifications. Ensure alignment with ongoing S/4HANA project design and rollout plans. Architect and configure SAP QM solutions to meet business needs. Drive functional improvements and lead the deployment of new features. Coordinate testing phases including User Acceptance Testing (UAT). Prepare training materials and support user onboarding with e learning tools. Collaborate with stakeholders across business and IT teams to ensure successful delivery. Provide consultative leadership in pre sales engagements and solution presentations. Mandatory Skills: Bachelors or Masters degree in Engineering, Business Administration, or related field. 10+ years of hands on experience in SAP QM, including full lifecycle implementations. Strong experience with SAP S/4HANA (greenfield or brownfield projects). Proven ability to lead teams and manage project deliverables. Excellent effective communication, presentation, and stakeholder management skills. Experience with cross module integrations (e.g., PP, PM, EAM). Familiarity with LabWare LIMS is a plus. Deal Breaker Skill: Expertise in S/4 Quality Improvement Functional. Preferred Skills: Experience in validated environments and regulated industries. Knowledge of advanced planning solutions. Strong administrative capabilities and multitasking abilities. Willingness to travel as required (up to 25% travel frequency).

We are looking for a skilled SAP QM Functional Consultant to join our team. The ideal candidate will have deep functional expertise in SAP Quality Management (QM) module and will be responsible for implementing, configuring, and supporting QM processes in line with business requirements. This role involves working closely with cross-functional teams to ensure quality standards and compliance across manufacturing, procurement, and supply chain functions. Key Responsibilities: Lead the analysis, design, configuration, and implementation of SAP QM module based on business needs. Collaborate with business users to gather and understand quality management requirements. Map business processes to SAP QM functionalities including Quality Planning, Quality Inspection, Quality Control, and Quality Certificates. Configure QM components such as Inspection Plans, Quality Notifications, Quality Certificates, and Lot & Serial Number Management. Support integration with other SAP modules like MM (Materials Management), PP (Production Planning), SD (Sales and Distribution), and PM (Plant Maintenance). Conduct workshops and training sessions for end-users and provide post-implementation support. Develop functional specifications and work with ABAP developers for custom developments/enhancements. Perform system testing, integration testing, and support user acceptance testing (UAT). Troubleshoot and resolve functional issues, analyze root causes, and recommend solutions. Maintain documentation of configurations, business processes, and procedures. Stay updated on SAP QM best practices and recommend continuous process improvements. Support data migration and validation activities related to quality management. Assist in change management and communicate updates to relevant stakeholders. Required Skills and Qualifications: 7 to 12 years of experience as a SAP QM Functional Consultant with full lifecycle implementation experience. Strong knowledge of SAP Quality Management module including quality inspections, quality notifications, inspection lots, and quality certificates. Experience in SAP QM integration with MM, PP, SD, and PM modules. Hands-on experience with configuration and customizing in SAP QM. Ability to analyze complex business processes and translate them into SAP QM solutions. Experience in preparing functional specifications and collaborating with technical teams. Good understanding of quality standards, ISO compliance, and manufacturing quality processes. Strong communication skills with the ability to liaise effectively between technical and business teams. Experience working in Agile or Waterfall project methodologies. Ability to work independently and as part of a team. Preferred Qualifications: SAP QM certification is a plus. Exposure to SAP S/4HANA QM module. Experience in industries such as manufacturing, pharmaceuticals, or automotive is preferred. Knowledge of SAP Quality Management reporting and analytics tools. Compensation & Benefits: Competitive salary package commensurate with experience. Health insurance, performance incentives, and other benefits. Opportunity to work in a dynamic and growth-oriented environment.

Quality manager required from a mobile accessories company Qualification - any electronics Exp- min 10 yrs salary- max 70000 Location - kundli, sonipat. Wtsapp me resume at 8295842337- Mr. Bansal

Responsibilities: Ensure compliance with regulatory requirements qa QMS knowledge Handle qa documentation &sop Lead IPQA activities and train staff Office cab/shuttle Free meal Food allowance Health insurance Annual bonus Provident fund Lactation rooms

Role & responsibilities 1. Establishment and implementation of harmonized Quality Management Systems at all API plants. 2. To perform Self-Inspection and routine audit in all the API plants, R&D and subsidiaries of Akums. 3. To ensure compliance as per current regulatory requirements at all the API plants, R&D and subsidiaries of Akums. 4. Preparation, review and implementation of CQA SOP's at all API Plants of Akums. 5. To involve in regulatory audits along with site team and to ensure compliance submission within timeline. 6. To review investigation for elimination of Market complaints and support plant team to handle market complaints. 7. To co-ordinate and organize Corporate Quality Management Review meeting of API plants of Akums. 8. To raise queries and discussion with senior to resolve queries on daily basis. 9. SOP validation & implementation Preferred candidate profile • CQA Experience in Pharma- API industry will be preferred • Must have good understanding about WHO GMP Perks and benefits Salary no bar for deserving candidates.

-Lead, manage, and continuously improve the Quality Management System (QMS) at the Gundulpet facility near Mysore. -Ensure compliance with global food safety standards, statutory requirements, and customer specifications. Required Candidate profile -Proven track record in managing BRC audits (mandatory) along with other international certifications. -Strong knowledge of global food safety standards, HACCP, GMP & regulatory frameworks

-Lead, manage, and continuously improve the Quality Management System (QMS) at the Gundulpet facility near Mysore. -Ensure compliance with global food safety standards, statutory requirements, and customer specifications. Required Candidate profile -Proven track record in managing BRC audits (mandatory) along with other international certifications. -Strong knowledge of global food safety standards, HACCP, GMP & regulatory frameworks Perks and benefits Food & accomodation provided by the company

We're seeking a Head of QA to lead our IATF 16949 implementation. The role requires experience in plastic injection molding, and involves overseeing quality, implementing processes, and ensuring compliance. Health insurance Performance bonus Provident fund Gratuity

Role & responsibilities Manager-Quality & MR. 10-18 years of relevant experience, a minimum of 5 years in managing a team. Experience in Composites or Aerospace desirable. Must have worked as Management Representative for the Organizational Quality for AS-9100. Experience and knowledge in AS-9100 and NADCAP procedures. Experience and knowledge in Operational quality processes Line inspection, raw material, and final product. Experience and knowledge in Lean Management, Six Sigma, Kaizen Experience and knowledge in problem-solving techniques, root cause analysis, and quality tools. BE in Mechanical or Aerospace Engineering, MBA desirable. Preferred candidate profile

Develop, implement, and monitor quality management systems in line with ISO, ASME, AWS, or equivalent standards.Prepare and execute PQP, ITP and Method Statements. knowledge of ISO 9001, welding codes (AWS, ASME), fabrication & erection standards. Required Candidate profile Experience in quality audits, inspections, NDT, WPS/PQR, and QMS implementation. Certification in Lead Auditor – ISO 9001/QMS is highly desirable.

Job Title: Solar Cell Quality Integrated PV Manufacturing Location: Kavali/Ramayapatnam, Andhra Pradesh (Location near to Nellore, AP) Position: Manager / Associate Manager /Deputy Manager Solar Cell Quality About the client: INDOSOL Solar Private Limited is a Special Project Vehicle (SPV) of Shirdi Sai Electricals Limited (SSEL), who is a leading Indian Conglomerate (Manufacturing B2B) in Transformer manufacturing, headquartered in Hyderabad. Having qualified in PLI (Production linked incentive) scheme through MNRE, Government of India is keenly materializing to set-up 10GW Integrated PV manufacturing for the entire value chain (Polysilicon, ingot, wafer, cell, Module & Glass manufacturing). Currently, this position is for their 1GW Module facility. Job Purpose The Incumbent will be part of solar cell quality function and will be responsible to drive the Quality department through best practices & innovative methods. He/ she will work closely with the other department functions to define all the necessary process and control procedures to meet product functionality, quality and reliability requirements. He/ she will be self-motivated and with good ethics and dedication to be a part of engineering team working on strategic ambition to be the world leading Integrated PV Manufacturer. Essential Duties & Responsibilities: To develop the processes and procedures to implement and establish the complete quality control procedures and guidelines for the inspection of solar Cell manufacturing, from incoming quality to finished good. Lead a team of quality engineers, providing guidance, training, and support to ensure accurate and consistent quality inspection procedures. To conduct regular audits/surprise checks/inspections of cells, ensuring statutory and regulatory compliance with respect to industry standards. To analyse the complete plant data to acquire trends, patterns, and areas for improvement. To collaborate with cross-functional teams, including engineering, manufacturing, and operations, to address quality issues and implement corrective actions. To maintain documentation related to inspection processes, including inspection reports, findings, and corrective actions taken. To monitor supplier performance and conduct audits to ensure compliance with quality standards and contractual requirements. To stay up-to-date on industry trends, technological advancements, and regulatory changes related to solar cell inspection. To drive continuous improvement initiatives to enhance the efficiency and effectiveness of solar cell inspection processes. He / She will be responsible for all levels of Quality Assurance including Incoming Quality Control, In Process Quality Control and Final Quality Assurance of the Solar Cells. Product and process audit to ensure the stability of process and quality of product at each stage of Solar Cell modules manufacturing process & measure the process performance. MIS Preparation and ISO/IMS Documentation to prepare the Various Quality Reports and maintain the activity of Document Control as per the requirements of ISO 9001, ISO 14001, OHSAS 18001. Complete Accountability & Inspection of Visual, Electrical and Final Quality Parameters of the Solar Cell. Improvement in production process to reduce rework, rejections. Man power management with proper utilization to get maximum efficient output. Responsible for maintaining quality standards across projects carrying out inspection, Customer audits & third party inspection. Responsible for monitoring defined inline process quality, process parameters of cell line tools in production line Involved in trials towards improvement of Cell performance Root cause /FMEA / SPC / 7 QC tools analysis of process/Production/Quality Issues associated with Cell Production line Handling and Calibration of Cell Sorter and other measurement tools of Four Probe, EL, and Life time scanner, Core scan tester Preparation of Quality MIS and Analysis on CTQ Parameters and Cell performance. On Job training to shop floor Operators for corrective actions of issues Implementation of TQM Concept on Shop Floor like 5S. Required Qualifications Bachelor's/Masters degree or above in Electrical/ Electronics/ Mechanical/ Material/ Production engineering with a Minimum 8-15 years Industry experience leading quality function in Tier 1 Solar Cell manufacturing companies or Electronic or Semiconductor Assembly industries. Candidates having experience in PERC/TOPCon/HJT Cell technologies will be highly desirable.

Responsibilities: * Manage QMS implementation & maintenance * Conduct process audits & ISO audits * Develop & implement quality strategies * Collaborate with cross-functional teams on improvement initiatives

Implement QMS, Conduct Internal Audit & MRM, Prepare the Process & Product Audit Plan, Co-ordinate for customer audit and external audit. 5S audit, Monitoring, MIS reporting, Maintain VSA audit, 4M analysis, MACE Activity documents review, Required Candidate profile Graduation in Engineering, Quality Management, or related field. Certified Lead Auditor for ISO 9001 and/or IATF 16949. Strong communication, analytical, and problem-solving skills.

About The Role About the team: ZF''s Commercial Vehicle Solutions (CVS) division helps shaping the future of commercial transportation ecosystems. Our mission is to be the preferred global technology partner for the commercial vehicle industry.What you can look forward to as Assistant Manager/Senior Engineer: Handling supplier for routine issues and daily NC management.. Handling daily quality issues with supplier and on time closer of issues with CAPA. Closely Working with supplier for process Audits/ improvement to get zero defect. Implementation of ZF DNA principles at supplier end to build quality culture. Prepare, Monitor and maintain supplier report. Coordinate and drive change management with internal and external stake holder Responsible for APQP launch, PPAP and drive new development activity. Responsible for supplier performance/PPM within business target. Your Profile as Assistant Manager/Senior Engineer: Must have experience of Supplier Quality. BE/Diploma in Mechanical/Automobile/Metallurgy, 6 to 10 years of experience. Knowledge of Quality Core Tool, IATF/ISO. Knowledge basic manufacturing process (casting, forging, rubber molding, Coating, Platting, Tube manufacturing, etc.) This position needs to work between ZF & Supplier Knowledge of APQP, PPAP,8D, QRQC.Handling supplier Audits, VDA 6.3 lead Auditor will be added advantage.

Manage the Quality Assurance function at manufacturing site Ensure compliance with ISO, GMP & REACH standard Develop, implement & monitor Quality Management Systems including SOPs, documentation & CAPA systems Handle customer complaints, conduct RCA Required Candidate profile 12-20 years of experience in QA, preferably in specialty chemicals Knowledge of analytical instruments, QC processes & technical documentation Strong knowledge -ISO 9001, GMP & other quality standards

1. Quality Management System Formulate and implement Varroc Quality Management System and facilitate continuous internal process and system improvement Monitor review activities to sustain certification requirements of the customers, including self-audits and audits by customers. Facilitate certification by external third-party agencies such as International Automotive Task Force (IATF) through yearly plant surveillance audits Coordinate observations from all plant audits through Plant QA Lead and Plant Head for reporting and submission to the customer 2. Customer Quality Assurance Manage customer complaints through supervision of plant quality leads, including implementation of corrective actions to ensure issues are not repeated Manage warranty cost reduction by implementing system improvements to reduce early failure rate of parts Manage customer satisfaction scores improvement through reduction or rejection reduction PPM (parts per million - internal, external) Participate in meetings with customer quality assurance representatives 3. New Product Development Develop quality management processes as per the requirement of the customer for the new part Ensure submission of production part approval process by overseeing testing with R&D and ME and participating in weekly reviews Ensure continuous improvement to quality by overseeing kaizens, and other improvement techniques, throughout the product life 4. Regular Production Lead weekly operations meetings attended by the BU Head and Strategy Lead to address any issues/concerns pertaining to quality at the plants Design mechanism for component testing and process testing and implement in plants Oversee plant quality leads to conduct testing on the line and final inspection of parts Enforce mechanism to improve supplier performance, including any major supplier issues which are affecting part quality and customer matrix 5. Team development Participate in recruitment process to identify the right talent across positions within the function Establish individual performance expectations and regularly review individual performance of the team Identify and create development opportunities for team members to enhance functional knowledge

Maintain accurate documentation of all QA/QC activities and test results Demonstrate attention to detail in all QA/QC tasks Proactively solve problems related to quality assurance and control

Responsible for meeting compliance of system and process as per QMS requirement, meeting compliance of customer specific requirement and to manage smooth & efficient functioning of incoming quality. Required Candidate profile Manage smooth & efficient functioning of incoming quality with adequate manpower development and their safety. Ensure costs are reduced and budgets are made effectively