235 Qms Implementation Jobs - Page 9

Role & responsibilities Conducting and Documenting Internal and Refresher Trainings Training Coverage and Participant Documentation Issuance and Retrieval of QMS Formats (OOS, Change Control, Deviation, Calibration) Collection, Review, and Archival of Calibration Records Compliance with ISO/IEC 17025, ISO 17034, and ISO 9001 Requirements Issuance and Archival of Instrument Usage and Calibration Logs Preparation and Control of Master SOPs, Specifications, and STPs Withdrawal and Return of Superseded Master Documents Preparation and Distribution of TDS Masters for New Samples Preparation of Protocols and Reports for Qualification/Validation/Verification/Method Transfer Completion and Verification of QMS Monitoring Formats (e.g.,Temp & Humidity, Data Backup) Review of Audit Trails for GxP Computerized Systems Preferred candidate profile Bachelors or Master's degree in Science or related field. Professional certifications related to Quality Management Systems (QMS), ISO standards, or calibration (e.g., Six Sigma, ISO 9001 Lead Auditor) are an advantage

At present average onsite utilization of Rajkot team is > 90% and we will ensure after addition of new resource. Janak bhai who was IMS auditor has resigned & need to fill up his vacant place. Roles and Responsibilities Should be responsible for audit/ quality for various industry for IATF, ISO 9001, other standards as Quality Assurance / Management Representative Audit planning Branch other operation supports Minimum 5-7 yrs. experience in automotive industry Implementation experience in on IATF & ISO 9001 Lead auditor qualification in ISO 9001. Experience in conducting internal audits Internal auditor IATF Internal Auditor ISO 9001

Application invited for ISO & QMS Lead Auditor JOB TYPE : Freelance engagement / Consultancy Location : INTEROCEAN, Mohan Estate Industrial Estate, Near SARITA VIHAR Job Description Exposure in Implementation and maintenance of ISO 9001:2015 requirements through Bureau Veritas certification body. Conducting Internal Audits as per Audit plan Conducting Management Review Meetings as required Witnessing and getting External Audits cleared Updation of ISO system (Manual, Formats, Procedures etc.) when required. Conducting ISO Awareness trainings Guiding Staff about implementation and assisting in making records (Quality Objectives, Continual Improvement Records and related reports). Preparing all relevant (Internal Audit & MRM) records as per system requirement Travel to Port Offices and conducting Internal Audits. Skillset required: Education & Certification: Required relevant degree & professional certification or training course pertaining to ISO Standards, Quality management, Environmental Management, or Occupational Health and Safety. Interested candidates, please mail your cvs at pooja.budhiraja@interocean.in

Acquire prospective customer from food & agri industries for business. End-to-end handling of QMS.FSMS & other systems Certification for the customers which includes training, documentation, implementation & audits of prospective clients. Annual bonus Work from home Travel allowance Job/soft skill training

Oversee the entire quality assurance process, from raw materials to finished goods, ensuring consistent quality & compliance, ensuring that products meet regulatory requirements & quality standards like ISO 13485, ISO 9001, 21 CFR 211 & 21 CFR 820 Required Candidate profile Bachelors in science 10-15 years' experience in quality in medical device/ pharma industry QMS implementation experience Must have regulatory audit exposure Like WHO/ USFDA & EU GMP

QMS - Manager Should have knowledge of IATF MACE / VSA VDA should be from forging industry of automotive background know how of all forging defects should have background of customer interaction knowledge of heat treatment process

Role & responsibilities Review, improve and implement existing Quality processes and procedures and KPIs to ensure it is aligned to create highest product quality and highest customer service. Drive improvements in all areas of operations, focusing on key performance indicators and key divisional processes. Support plants as necessary with root cause analysis, problem solving and drive consistent improvements. Assist plants with the deployment of corporate quality policies, auditing practices and ensuring adherence to company's Quality and Regulatory strategies in accordance with the established strategic plan. Assist plants with deployment and implementation of customer requirements and specifications as applicable. Ensure communication between plants and sharing of best practices and lessons learnt - for consistent customer support and representation for global accounts. Essential Functional Requirement Seasoned and competent Quality professional with over 10+ years of experience. Experience with auto component manufacturing companies; preferably having a high volume-low value product portfolio. Significant experience in turnaround strategies for quality improvement as well as leading wins for Quality Awards / Certifications. Qualified engineer with certifications in relevant quality systems ISO / TS / IATF / Six Sigma etc. Total Quality Management Professional (TQMP) brining hands-on experience of leading TQM, Manufacturing Excellence implementation in an organisation. Preferred candidate profile Educational Qualification: Bachelor of Engineering (Mechanical or Metallurgy) Experience: 10+ Years Any additional requirement: Specify Candidates current Designation for search & right fitment: Head Quality, Head QMS, Head Manufacturing Excellence Preferred Industry Type: Automotive

Position Deputy Manager - Quality Assurance Experience: 7 - 14 Yrs Function: Product & Technology Development Primary Responsibilities: The incumbent will be responsible for the design, implementation, and verification of quality systems across food manufacturing units. Key duties include centralized monitoring of key process and quality performance indicators and reporting through the Management Information System (MIS). The role also involves preparing detailed product trial quality reports and compiling comprehensive documentation (dockets) to facilitate technology transfer to production units. Requirements: Proven knowledge and experience in food quality system design, implementation, and verification. Strong understanding of process control validations in relation to product performance. Familiarity with food safety standards and protocols, including HACCP, ISO, GMP, and related frameworks. Exposure to process automation and quality automation systems is highly desirable. Proficiency in preparing and managing documentation related to quality systems and food safety plans, including procedures and standardized formats. Prior experience in a production environment will be considered an advantage. Competency in using software applications for effective MIS reporting is essential.

Role & responsibilities To Monitoring Customer Complaints & minimizing complaints through action taken. To Monitor all area PPM (Final Inspection & escalation to respective areas for improvement & provide support to achieved defined targets. Responsible for adherence of Quality management system & align with TS 16949/Customer requirements on monthly basis. Effectiveness Monitoring of Corrective & preventive action plan. Improve Customer Rating. Preferred candidate profile Btech Mechanical with 19+ years of work experience in Automotive Industry. Leadership quality, Analytical skills, knowledge of quality tools, Communication skills, Presentation skills 5 S & Safety audits

Hiring Quality Head for Leading PMC in Navi Mumbai Roles and Responsibilities Conduct quality audits, inspections, and reviews to ensure compliance with ISO standards and company policies. Develop and implement effective quality control procedures for construction projects. Lead and manage the QA/QC department, including setting quality goals, SOPs, and best practices. Collaborate with project teams to identify areas for improvement and implement corrective actions. Ensure accurate documentation of quality records, reports, and certificates. To handle multiple projects /To lead department Must have exposure of handling Real Estate, Industrial & Infra projects Desired Candidate Profile Strong knowledge of ISO systems implementation and auditing principles. B.Tech/B.E. degree in Civil from a recognized university. 15-24 years of experience in civil engineering or related field with expertise in QA/QC, quality audit, internal quality auditing, etc. Excellent communication skills with ability to work effectively at all levels within an organization. To apply, please send your resume with following details Mail to: harshala.kadave@gemengserv.com Subject Line: Application for Quality Head @ Mumbai Total Experience: Current CTC: Expected CTC: Current Location: Notice Period: Reason for change:

Manage the Quality Assurance function at manufacturing site Ensure compliance with ISO, GMP & REACH standards through robust QMS implementation, audits & CAPA systems Required Candidate profile 8–12 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

Responsibilities: As a A Quality Management System (QMS) Engineer * Develop & maintain quality docs, including compliance with industry standards * Implement QMS,IATF, ISO standards, PPAP Process t audits. continuous improvement initiatives Provident fund Annual bonus Food allowance Health insurance Office cab/shuttle

Knowledge of sheet metals & machinery components. Knowledge of PPAP, APQP, SPC, MSA, FMEA Knowledge of ISO 9001, IATF, EMS, OHSAS knowledge of MIS data collection, MAC audit system knowledge of top management MRM 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.

Role & responsibilities Handling and management of the Engineering department. Overall responsible for the maintenance of the plant, Machinery, Utilities, Building, and premises Coordination with concerned department heads for the timely execution of engineering activities. Planning and scheduling preventive maintenance of Production, QC, Warehouse equipment, and utility as per the preventive maintenance planner. Review of SOPs, protocol & reports, and preventive maintenance planner and checklist. To provide technical guidance to the engineering team and top management. Responsible for the selection and design of equipment, plant layout, materials handling, and ordering of material. Up-dation of facilities as per regulatory guidelines such as man material handling, HVAC system and utility etc. The monitoring of compliance with the requirements of Good Manufacturing Practice. Handling of QMS activities related with engineering department. Ensure that environmental, Health and Safety, Engineering, Quality standards and procedures are adhered to review the technological system that supports a more environmentally friendly approach. Requirement and skills: Proven working experience as a Manager-Engineering. People-oriented and results-driven. Candidates having pharmaceutical experience of working in liquid and tablet products, Equipment, utility, and maintenance will be the preference. Preferred candidate profile Applicants must be stay in Modinagar (Ghaziabad).

FOUNDRY Cast Iron Foundry In charge Strong Background in Cast Iron Green Sand Foundry Ensuring Rejection as per Targets & Driving Continual Improvement any Quality Issues related to Metallurgy Responsible and Monitoring driving continual improvement Required Candidate profile BE Mech/ Metallurgy Strong Background in Cast Iron Green Sand Foundry10~12 Years of Experience SAP PP Module and driving inventory management program QMS & EHS Implementing Safety Controls Compliance

Customer complaints management , Customer satisfaction Reduce the cost of poor quality Support to new development project Implement cost saving projects Implement cost saving projects Implement QMS Training and awareness Required Candidate profile knowledge of process improvement tools / techniques such as 6 sigma, VDA / Lean manufacturing team leading experience with Audit and Supplier quality

Job Title: Quality Engineer Department: Quality Department Location: Chakan, Pune Reporting To: Manager Job Description: We are seeking a motivated and detail-oriented Quality Engineer to join our Quality Department. The ideal candidate will have relevant experience in ISO standards implementation and in-process inspection. This role involves supporting the planning, execution, and follow-up of internal and external audits, maintaining compliance with ISO standards, and driving continuous improvement in quality systems. Key Responsibilities: Assist in the implementation, maintenance, and continual improvement of ISO standards: ISO 9001, ISO 45001, and ISO 14001 . Plan and coordinate internal and external audits , including third-party and surveillance audits. Conduct in-process inspections to ensure adherence to quality requirements at all stages of production. Identify process non-conformities and assist in the root cause analysis and corrective action implementation. Maintain and update documentation related to Quality Management Systems (QMS) , Environmental Management Systems (EMS) , and Occupational Health and Safety Management Systems (OHSMS) . Coordinate with various departments to ensure compliance and system effectiveness . Prepare audit reports, maintain audit records, and track closure of audit findings. Support training and awareness sessions related to quality and ISO standards. Participate in continuous improvement initiatives to enhance overall system efficiency and product quality. Candidate Requirements: Education: Diploma/Bachelors degree in Engineering, Quality Management, or a related field. Experience: 15 years in a Quality role with exposure to ISO standards and in-process inspections. Technical Skills: Working knowledge of ISO 9001, ISO 14001, and ISO 45001. Familiarity with audit processes and documentation. Hands-on experience with in-process inspection tools and techniques.

HIRING FOR SENIOR LEADERSHIP POSITIONS PHARMA MANUFACTURING Credo Signature Solutions is inviting applications for Two Prestigious Senior Leadership Roles with one of our esteemed pharmaceutical clients engaged in the manufacturing of tablets and liquid formulations. The manufacturing facilities are located across the Northern Himachal region and Punjab . 1. PLANT HEAD 2. QUALITY HEAD Key Requirements (Common to Both Positions): Minimum 20+ years of experience in the pharmaceutical industry Proven track record in a similar leadership capacity (Plant/Quality Head) Prior experience working with top 10 Indian pharmaceutical companies Strong leadership qualities with the ability to drive performance and foster cross-functional collaboration Thorough knowledge and hands-on experience in handling regulatory audits such as USFDA, EU-GMP, WHO, and other RoW markets Excellent interpersonal and communication skills Qualification: B.Pharm/M.Pharm/M.Sc or equivalent Additional Role Expectations: For Plant Head: Comprehensive understanding of end-to-end plant operations including Production, Quality, Engineering, Supply Chain, and EHS Ability to create synergy among departments and align them with business goals Strategic mindset with a focus on compliance, operational excellence, and people development. For Quality Head: Deep expertise in Quality Assurance, Quality Control, and Compliance Strong exposure to QMS, CAPA, data integrity, and regulatory documentation Capability to lead a large quality team and maintain a culture of quality and compliance across the site. Compensation: CTC in the range of INR 40 Lacs to 50 Lacs PA (negotiable for exceptional candidates) Location: Manufacturing sites in Northern Himachal Pradesh and Punjab. How to Apply: Interested candidates may share their updated resume at: info@credosignaturesolutions.com Only shortlisted candidates will be contacted for further discussions.

Role & Responsibilities * To ensure that the processes needed for quality management system are established, implemented and maintained. * Establish documentation of the organization in line with requirements of ISO 9001, API Spec Q1 and API 15LR in consultation with concerned process owner and ensure their adequacy. * Drive internal audits and co-ordinate external audits. * Ensure implementation of corrections/ corrective actions/ preventive actions as applicable. * Ensure effectiveness of actions taken. * Plan and ensure execution of periodic audits and initiate subsequent actions. * Co-ordinate management review meetings as per specified requirements. * Maintain relevant database. * Keep database of departmental measurable on periodical basis and put up to management. * Ensure control over documents and records as applicable. * Create and review technical training programs to meet organizational needs. This includes developing course content, objectives, and schedules. * Monitor and analyze the results of training programs. This includes evaluating the overall effectiveness of the program and making improvements. * Prepare training materials, such as presentations, worksheets, and course outlines. * Collaborate with other internal teams and stakeholders to develop course content and goals. * Maintain records of training activities, participant progress, and program effectiveness. * Collaborate with senior management to obtain necessary training resources. * Qualify the work force at site & plant level.

Position Summary The QMS Manager will lead the development, implementation, and maintenance of the organization's Quality Management System (QMS) within the fabrication sector. This role involves ensuring compliance with industry standards, driving continuous improvement initiatives, and fostering a culture of quality excellence. Expertia+1TE Connectivity Careers+1 Key Responsibilities QMS Development & Implementation Develop and implement quality management strategies and plans aligned with ISO 9001 and industry-specific standards. Establish and maintain quality documentation, including manuals, procedures, and work instructions. TE Connectivitys + 1 Energye + 1 Compliance & Auditing Plan, conduct, and manage internal and external audits to ensure compliance with QMS requirements and industry regulations. Support third-party audits and certifications. JobLeads+1TE Connectivity Careers+1 Process Improvement Identify opportunities for process improvement within the QMS and manufacturing processes. Collaborate with relevant departments to implement changes that enhance efficiency and quality. JobLeads+1TE Connectivity Careers+1 Corrective & Preventive Actions (CAPA) Lead CAPA programs to address non-conformances, ensuring timely resolution and documentation of root causes, corrective actions, and preventive measures. ORDNUR+3 Connectivity Careers+3 Training & Education Develop and deliver training programs to employees on QMS processes, regulatory requirements, and industry best practices. Ensure staff adherence to quality standards and procedures. SHRM+6JobLeads+6TE Connectivity Careers+6 Data Analysis & Reporting Analyze quality data, trends, and key performance indicators (KPIs) to report on the health of the QMS. Provide management with actionable insights to drive continuous improvement. JobLeads+1TE Connectivity Careers+1 Regulatory Compliance Stay up-to-date with changes in industry standards, regulations, and best practices. Ensure the company is compliant with current and future regulatory requirements. JobLeads Qualifications Bachelor's degree in engineering, quality management, or a related field. Minimum of 5 years of experience in quality management within the fabrication or manufacturing industry. Strong knowledge of quality management principles, tools, and methodologies. Experience with ISO 9001 or other quality standards. Excellent problem-solving and analytical skills. Strong leadership and interpersonal skills. Proficiency in using quality management software and tools. Ability to work effectively under pressure and meet deadlines. TE Connectivity Careers+3 Energy Jobline+3 Himalayas + 3 Preferred Qualifications Lean Six Sigma certification. Experience in the sheet metal fabrication industry. Proficiency in Microsoft Office and quality management software. Energye + 1 en.wikipedia.org+1gkmachine.com+1 Energye + 1 CONTACT NO :9487807964

Develop and implementation of the Quality Management System Deep knowledge of IATF 16949:2016, ISO 14001:2015 & ISO 45001:2018 Co-ordinate with external auditors Audit findings and NC closure Hyundai 5Star audit follow up Knowledgeof APQP, PPAP ISIR

Role & responsibilities Overall responsibility for monitoring of implementation, maintenance and improvement of Management Systems (ISO9001, IATF16949, AS9100D, ISO14001, ISO45001) To maintain the integrity of the Management Systems when the changes are planned and implemented such as new rules, standards, core tools, CSR, IATF Sanctioned Interpretations & FAQs To maintain the management system documents and records Liaison with external parties on matters relating to Management Systems such as quotation, agreements, audit plans, auditor travel & accommodation plans. Scheduling and conducting MRM Scheduling and conducting Internal Management System Audits Corrective action follow-up for all non-conformities raised during Certification body and internal management system audits To lead reviewing and implementing Customer Specific Requirements (CSR) To do centralized KPI monitoring related to Quality, Environment and Safety Preferred candidate profile

Role & responsibilities Hands-on experience in managing Quality Assurance activities in Manufacturing Sheet Metal / Other Fabricated products. To Develop and implement quality control plans, procedures, and standards for Sheet metal fabricated products esp. for the Electrical Industry. Handling a team of Engineers and Responsible for quality assurance at all stages viz., Inward, In-process & Final inspection and testing of the products. To handle customer complaints and identify areas of improvement and implement corrective actions. Responsible for Monitoring and controlling all the process parameters to be maintained to get good quality product. To have Strong knowledge in ISO 9001:2015 requirements and responsible for quality management system (QMS) compliance across all departments. To Handle Internal & External ISO Audits, Customer audits and other Product Test & certifications. candidate must have In depth knowledge in Analysis of Quality parameters and SPC tools. To Collaborate with cross-functional teams to resolve quality issues and improve product and process reliability. To Provide training on QMS principles, tools, and best practices to employees at all levels. Preferred candidate profile Candidate with 8-13 years of experience in QA Management and a B.Tech/B.E. degree in Electrical or Mechanical stream is preferred. Candidate having experience in Paint / Powder coating Quality assurance is added advantage. Candidate having exposure on Enclosure IP/NEMA testing and UL certification will be an added advantage.

Role & responsibilities Management System (ISO 9001) Implementation: Able to do process by process Gap assessment Establishment of Documentation, Preparation, review Providing awareness and facilitate ISO 9001 requirements implementation Coordinate and facilitate Management System certification audits with external bodies. Ensure readiness and compliance with certification requirements Conduct ISO 9001 internal audits. Identify non-conformities and implement corrective actions. Willing to travel in and around Coimbatore to visit customer places. Must have two wheeler. Preferred candidate profile Qualified ISO 9001:2015 Internal Auditor Proven experience in coordinating and executing Management System certification audits. Expertise in ISO 9001 or IATF 16949 internal audits. Strong knowledge of Quality Management Systems and effective implementation practices. Proficiency in root cause analysis, corrective actions, and preventive measures. Familiarity with 7 QC tools, Standard Operating Procedures (SOPs), and Control Plans. Excellent communication, organizational, and problem-solving skills. Perks and benefits - ESI - PF - Fuel Allowance - Yearly Bonus

Position Summary: We are seeking an experienced and proactive Quality Control Manager with a strong background in In Vitro Diagnostics (IVD) to lead and oversee all QC activities within our manufacturing and development operations. The QC Manager will be responsible for ensuring that IVD products meet internal quality standards and comply with international regulatory requirements. This role plays a key part in managing a QC team, improving processes, and supporting product development and commercial release. Role & responsibilities Lead and manage the Quality Control team, ensuring daily testing activities are conducted efficiently and in compliance with regulatory requirements (ISO 13485, FDA 21 CFR Part 820, and CE-IVD). Develop, implement, and maintain QC procedures for raw materials, in-process controls, and final product testing for IVD devices, including immunoassays, molecular diagnostics, and rapid tests. Oversee method validation, equipment qualification (IQ/OQ/PQ), and routine calibration and maintenance of laboratory instruments. Review and approve QC test results, reports, and batch records, ensuring timely product release. Manage investigations of non-conformances, deviations, out-of-specification (OOS) results, and implement corrective and preventive actions (CAPAs). Participate in cross-functional teams for new product development, transfer-to-manufacturing activities, and continuous improvement initiatives. Ensure compliance with GLP/GMP requirements and prepare for internal and external audits (e.g., ISO, FDA, notified bodies). Provide leadership, training, and mentorship to QC staff, fostering a culture of quality and accountability. Monitor QC metrics and KPIs, and report regularly to senior management. Maintain and improve the Quality Control Laboratory environment, including documentation, data integrity, and safety practices. Education: Bachelors or Masters degree in Biotechnology, Biochemistry, Microbiology, Life Sciences, or a related field. Experience: Minimum 610 years of experience in Quality Control, with at least 3 years in a managerial or supervisory role within the IVD or medical device industry. Skills: In-depth knowledge of IVD regulations and quality standards (ISO 13485, FDA QSR, CE-IVD). Strong leadership, team-building, and project management skills. Proven experience in implementing and improving QC systems and processes. Excellent problem-solving skills and experience with RCA and CAPA tools. Proficiency in LIMS, statistical analysis, and data management tools. Preferred candidate profile Experience with regulatory submissions, audits, and inspections (FDA, ISO, EU MDR). Familiarity with risk management (ISO 14971), design controls, and product lifecycle management. Quality certifications (e.g., ASQ CQM/OE, Six Sigma Green/Black Belt) are a plus