581 Qms Implementation Jobs - Page 13

Sessions on various Quality/Management System Mentor & coach companies using Omnex methodologies, deployment. Best in class systems, Problem Solving, APQP/PPAP/FMEA/Lean 6sigma. Undertake consulting/training for clients to ensure certification audits

We are seeking a skilled QMS Consultant. This role is critical in helping automotive manufacturers and suppliers adhere to IATF 16949, CQI 9/11/12/15/27 , GD&T , ISO 14001,ISO 45001,VDA standards by developing and implementing effective QMS Measures

DME/BE - Mech with at least 10-15 years of experience in automotive industries, Knowledge of IATF 16949,VDA 6.3, Pokayoke, Kaizen. Having ERP Knowledge shall be preferred.

To oversee and enhance the Quality Management System (QMS) within a sheet metal manufacturing setup—ensuring compliance with ISO/IATF standards, driving continuous improvement, and supporting customer satisfaction and operational excellence.

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 trac...

Role & responsibilities Maintain and implement QMS and EMS systems within the organization. Maintain quality and environmental Standards as per ISO-9000 (QMS) and ISO 14000 (EMS). Prepare all documents of Audit & provide control copy to each department and where ever applicable. Prepare Audit NC & take corrective & preventive action. Responsible for all Management Representative (MR) activity. Coordinate / collect data from each department and conduct MRM Meeting. Conduct internal Audit and External audit. Responsible for MPI/DP inspection, and coordinated with production team and ensure the results are delivered without delay. Responsible for all RT casting and complete follow up with RT in...

Develop, implement & maintain a robust Quality Management System (QMS) in compliance with applicable regulations (GLP, GCP, GXP, ICH guidelines) Create, review, and manage SOPs, work instructions, protocols, reports & documentation across departments Required Candidate profile 4+ years of experience in QA/QC within the pharmaceutical, biotech or drug discovery industry. Quality control certifications are preferred In depth understanding of QA/QC procedures & legal standards

1.Responsible for all floor QC,QA,QMS at plant 2, Team management, systems, work instructions and SOP adherence 3.ISO FSC, Sedex, 5S Audits and compliance 4 Ensure calibration of Lab Instruments as per NABL 5. CAPA,- RCA, report & corrective steps

Role & responsibilities Review and approve Finished Goods and corresponding Certificates of Analysis (COA). Maintain detailed records of received samples in an organized manner. Ensure proper allocation and storage of approved COAS in the shared drive. Verify and confirm drug product permissions as per regulatory requirements. Oversee the finalization of packing materials in coordination with relevant departments. Conduct audits of new vendors, ensuring compliance with quality standards. Ensure proper implementation of Corrective and Preventive Actions (CAPA) for any deviations or complaints. Visit manufacturing sites to address and investigate market complaints effectively. Coordinate with ...

Role & responsibilities Review and approve Finished Goods and corresponding Certificates of Analysis (COA). Maintain detailed records of received samples in an organized manner. Ensure proper allocation and storage of approved COAS in the shared drive. Verify and confirm drug product permissions as per regulatory requirements. Oversee the finalization of packing materials in coordination with relevant departments. Conduct audits of new vendors, ensuring compliance with quality standards. Ensure proper implementation of Corrective and Preventive Actions (CAPA) for any deviations or complaints. Visit manufacturing sites to address and investigate market complaints effectively. Coordinate with ...

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

DCM SHRIRAM RAYONS,KOTA JOB DESCRIPTION : MANAGERIAL POSITION, (Sr. Manager/ AGM) (QUALITY ASSURANCE) Location: Kota, Rajasthan Qualification: B.sc/M.Sc (chemistry), B.Tech Chemical/Textile/Rubber Technology Preferred Age: 40+ Years Experience: 20+ Years Location: Kota, Rajasthan Job Description: • Functioning of QCD and Chemical Laboratory – Updated Calibration status & adherence to scheduled testing, maintaining laboratory conditions and material clearance/ disposal decisions. • Process Control – SQC/SPC from Auxiliary to Dipping • Functioning of Management functions as per ISO – 9001, 14001 & 45001 in the unit. • Handling Customer Related matters – Conformance to committed actions, Root C...

Role & Responsibilities: Conduct third-party audits at client sites. Perform desk reviews of Quality Management System (QMS) documentation, including Batch Manufacturing Records (BMRs), Validation and Qualification protocols, and Standard Operating Procedures (SOPs). Provide comprehensive solutions for identified gaps or deficiencies during the review process. Ensure compliance with regulatory requirements and client standards. Preferred Candidate Profile: Expertise in handling Quality Management Systems. Skilled in reviewing Risk Assessments and investigation reports. Experience in analyzing and reviewing analytical data. Proficient in conducting third-party audits and preparing compliance ...

As a Hardware Engineer with over 10 years of experience, based in Udaipur, you will be responsible for designing, developing, and testing ATM hardware. Your role will involve working on mechanical designs to ensure compliance with industry and customer standards. Collaboration with software teams for system integration will be a key aspect of your work. An essential part of your responsibilities will include implementing and maintaining Quality Management Systems (QMS). This will involve conducting audits, defining quality procedures, and setting standards to ensure the highest level of quality in all hardware products. Proficiency in speaking and reading Japanese is a must due to the biling...

Trackwise Consultant Experience: 5 to 8 Years Location:- Bangalore/Pune/hyderabad Notice period : Immediate to 15days Job Description Knowledge of Trackwise is a must Should have indepth knowledge of handling Quality management in TrackWise Should have a strong understanding of Trackwise Business processes such as Change Management System IncidentDeviation Investigation CAPA implementation etc Should have a deep understanding of the individual workflowsapprovals in each Trackwise Module Experienced in generating various types of queries in TrackWise requirements Well versed knowledge of Quality Risk assessment through TrackWise Application Should have managed QMS implementation projects incl...

JOB DESCRIPTION SUMMARY: Owns Quality of value stream, compliance, internal audits, zero defect initiative, customer issue resolution (problem solving), customer satisfaction (NPS), and CoQ governance. Manages local QMS (quality management system) to ensure the continuous production of products consistent with established standards. Coaches, supports, instructs, and ensures the commitment of local management to operate at a high level of capabilities effectively. Follows company safety policies and procedures. ESSENTIAL DUTIES: Demonstrate leadership in communicating business goals, programs, and processes for various business functions. Utilize your experience or expertise to solve problems...

Post- Quality Documentation Specialist Location - Pune Chakan Contact - 9356395439 Email - punejob2025@gmail.com Experience - 05-10 yrs Skills Certification in ISO 9001:2015 Internal Auditor or Lead Auditor. Prior experience in the renewable energy or heavy fabrication sector. Knowledge of ISO 45001 and ISO 14001 standards. Strong knowledge of APQP, PPAP, FMEA, Control Plans, and Process Flow Diagrams. Experience with ISO 9001 audits and OSHA safety documentation standards. JD Quality Documentation Specialist to manage and improve our documentation systems in line with industry standards. The ideal candidate should possess hands-on experience with PPAP, APQP, ISO audits, and OSHA documentati...

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 ...

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 re...

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 clien...

Replacement hire- please arrange for the above post at the earliest. Roles and Responsibilities Job Description: Assistant Manager - Quality Assurance, Environment and Energy - Certification Body Objective : The Assistant Manager - Quality Assurance (QA) for Environment & Energy ensures compliance with international accreditation standards, maintains robust Quality Management Systems (QMS), and supports the effective execution of validation, verification, and certification processes for climate change and GHG-related schemes Key duties: Ensuring the quality of project delivery for Climate Change and GHG projects under CB/VVB Maintaining and updating documentation for Climate Change project s...

Job Purpose : (what contribution is this position supposed to make in business?) The QMS and EU MDR Compliance Executive is responsible for ensuring compliance with ISO 13485, EU MDR (Regulation EU 2017/745), and other applicable quality and regulatory requirements. This role will support the development, implementation, and maintenance of the Quality Management System (QMS), oversee documentation control, conduct internal audits, and support regulatory submissions and audits as required. Key Deliverables/Responsibilities of this position 1- Quality Management System (QMS): Maintain and improve the ISO 9001:2015 / ISO 13485:2016-compliant Quality Management System. Ensure effective implement...

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 Mana...

Quality Mgr (must Grey / Iron casting- Pillaipakkam (Foundry Divi) Exp: 15+yrs Edu: Diploma/ BE Short notice preferable Interview date:19th Jul(Saturday) PAP, CFT,APQP,Heat treatment,Quality stand. CV- lifeturnmgmt6@gmail.com /7358656750 - What app

Requirement for Injection Molding Company Responsibilities: * Lead QMS implementation & maintenance * Ensure compliance with ISO, IATF standards * Manage PPAP documentation process * Oversee quality control activities