428 Qms Implementation Jobs - Page 15

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

Role & responsibilities To lead and manage the Quality Control function, ensuring all packaging materials and finished products meet internal specifications, customer requirements, and industry standards. Preferred candidate profile Lead and manage the QC team across all shifts. Inspect raw materials, in-process, and finished goods for compliance. Define and implement QC procedures, test methods, and standards. Maintain and calibrate testing equipment and instruments. Investigate quality issues and implement corrective and preventive actions (CAPA). Coordinate with production, design, and dispatch teams for quality assurance. Prepare quality reports, trends, and improvement plans. Train operators and QC staff on quality parameters and SOPs. Ensure compliance with ISO, GMP, and customer audit requirements. Handle customer complaints related to product quality.

Handling of ISO, IATF and other required certifications and all QMS systems. Handling customer audits and QMS queries. Responsible for heading a team of chemists Required Candidate profile Proper knowledge of QC SOP, MOA, Specification, BIS, ASTM, physicochemical Analysis and ISO documentation. Operating equipments like AAS, Surface Area Analyser, pH Meter etc.

Own, maintain, and continually improve the plant-wide Quality Management System (QMS) to guarantee that every toy leaving the line meets Indian BIS guidelines, international toy-safety standards, and customer expectations. Drive a zero-defect culture

Role & responsibilities - Inspection and Testing: Conduct regular inspections of incoming materials, in-process production, and finished products to ensure compliance with quality standards. Data Analysis and Reporting: Analyze data to identify trends and areas for improvement, and generate reports on quality performance metrics. Problem Solving: Investigate customer complaints, identify root causes of issues, and implement corrective actions to prevent recurrence. Process Improvement: Collaborate with other departments to develop and implement continuous improvement initiatives to enhance quality and efficiency. Quality System Development: Develop and implement quality management systems, ensuring compliance with industry standards and regulations. Supplier Management: Work with suppliers to address quality issues, improve supplier performance, and ensure consistent quality of materials. Documentation and Record Keeping: Maintain accurate records of inspections, tests, and corrective actions, and prepare documentation for quality management systems. Training and Communication: Provide training to other employees on quality standards and procedures, and communicate quality information effectively throughout the organization. Skills and Qualifications: Education: Bachelor's degree in Engineering or a related field. Experience: Proven experience in quality engineering or a similar role. Knowledge: Strong understanding of quality management systems, inspection techniques, and quality control procedures. Skills: Analytical skills, problem-solving skills, communication skills, and the ability to work effectively in a team. Certifications: ASQ Certified Quality Engineer (CQE) certification can be beneficial. Specific to Heavy Structure Companies: Knowledge of Construction Materials: Understanding of materials like steel, concrete, and other materials used in heavy structures. Weld Inspection and Testing: Familiarity with welding procedures, quality control methods, and non-destructive testing techniques. Structural Integrity: Ability to assess the structural integrity of completed structures and identify potential defects. Compliance with Industry Standards: Knowledge of relevant building codes, standards, and regulations, such as those from the American Welding Society (AWS).

Role & responsibilities - To Monitor Working of Quality Department Incoming, In process, Outgoing. - To ensure timely completion of new projects for customers - To control process sheets and process changes - To audit working of quality department - To monitor statistical process control - Raw material / product development sample management Verification - Carry out and monitor quality and cost improvement initiatives - Responsible for conformity to product requirements have the authority to stop shipment and stop production to correct quality problems - To ensure the customer requirements are met - Conduct Internal Quality Non- Conformance Review - IATF -16949 audit certification renewal - Secondary supplier status analysis - FMEA, APQP, Incoming Inspection, Internal& External Failure Verification - New product and New development report with management approval - Evaluating NC point & Countermeasure submission to the customer - Maintain the mixing ration history for tracking - Verification. - Existing and new raw material MSDS report – Validation - New raw material supplier 4M changes report reviewed Preferred candidate profile - Customer specification test standard – Validation - DQC will be checked on weekly & monthly - Improve the product quality analysis report verification and implementation. - Zero Rejection - verification of daily production product. - Quality tracking system verification. - Basic Lot Test & Long-term Test Result - Validation. - Incoming RM /Product Improvement status analysis - Inward Inspection report - Validation. - Daily production test - Result validation. - Product Revalidation report – Review - Lot Test report for each product – Review - Existing product improvement result Review - Line problem and customer improvement analysis - Customer Quality audit support. Perks and benefits Yearly Bonus: Twice in a Year (120% on Gross) Travel Facility: Gummidipoondi to Madhavaram Food Allowance: Free of cost twice per day Special Allowances: Benefits for marriage, new born babies & other scenarios. Accommodation: Provide free Accommodation for Bachelors Other Benefits: PF, ESI & Group Medical Insurance.

Role Summary: OSD Production QMS is responsible for ensuring adherence to quality standards within the production process. The role involves monitoring production activities, implementing quality control measures, maintaining compliance with regulatory requirements, and driving continuous improvement initiatives. Roles And Responsibilities Quality Compliance: Implement and monitor compliance with QMS standards Industry-specific standards. Conduct periodic audits of production processes to identify deviations and enforce corrective actions. Ensure all production processes align with regulatory and company quality standards. Documentation & Reporting: Maintain and update standard operating procedures (SOPs), work instructions, and quality records. Prepare detailed reports on quality performance, including non-conformance incidents and corrective actions taken. Process Improvement: Analyze production workflows and recommend improvements to enhance efficiency and quality. Participate in root cause analysis for production issues and implement preventive measures. Key Skills and Competencies: In-depth knowledge of Quality Management Systems and standards. Strong analytical and problem-solving skills. Excellent communication and interpersonal abilities. Proficiency in using quality management tools and techniques. Familiarity with relevant USFD, EU, TGA regulatory requirements and industry best practices.

Job Description: QMS Executive Qualifications: Bachelor's degree in Computer Science, Information Technology, or related field. 1-3 years of relevant experience in Quality Management Systems (QMS). Preferred certifications: ISO 9001 Internal/Lead Auditor, ISO 27001 Internal/Lead Auditor. Skill Set: Knowledge of Quality Management Systems (QMS). Familiarity with ISO standards 9001 and 27001. Proficiency in reviewing/auditing internal projects and documentation. Exposure to Configuration Management Systems (e.g., SVN). Understanding of RCA (Root Cause Analysis) and CAPA (Corrective and Preventive Action). Knowledge of software development methodologies. Excellent communication and documentation skills. Proficiency with MS Office tools. Responsibilities: Maintain and update document repositories related to QMS and ISMS. Ensure the master list of QMS documents is up-to-date. Support the QMO team in tasks assigned by the QMS Manager. Collect and analyze QMS-related data from project teams (e.g., best practices, metrics). Plan, execute, and report internal quality audits and track findings to closure. Review and suggest improvements for QMS/ISMS documentation. Assist in training coordination for Quality Management and ISMS. Support teams in implementing QMS processes during project lifecycle stages. Maintain records for customer feedback, CAPA management, and internal audits. Participate in Management Review Meetings (MRM) and monitor action item status. Coordinate with teams / departments during third-party audits and ensure compliance.

Implement the IMS procedure, Formats & Supporting Document and ensure at the point of use/Conduct regular audits to improve the IMS processes/Manage the audit non conformity data base and detailed analysis of Non conformities/Conduct DRM & MRM Required Candidate profile The candidate should have the VDA certified auditor and should have minimum 6 Years experience in QMS.

Seeking a IPQA Executive to ensure skincare products meet regulatory, safety, and quality standards. Work closely with manufacturing, R&D, and QC teams. Requirement: 2+ years of QA experience, preferably in cosmetics or pharma manufacturing. Required Candidate profile Skincare manufacturing & QC expertise Knowledge of FDA, GMP, ISO regulations Attention to detail & procedural compliance Strong analytical, problem-solving & com skills Ability to work with GMP proces

Manage QMS Act as managment representative for IATF and EHS Requirements exp in QA Roles ideally in the seals or mechanical components industry strong understanding of IATF 16949 ISO STANDERDS EXP IN RUBBER STEEL INDUSTRY REQUIRED 9812001068

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 Coordinator Quality & Compliance (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: Bachelors degree in Engineering, Science, or Business Administration (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

Job description Should have sound knowledge of QMS System and Change Control, Deviation and CAPA Procedure. Review of Preventive maintenance & calibration of equipment and systems. Investigation and closure of all deviations, OOS and complaints

Responsible for DOJO Training, Induction and Orientation, Training documentation for internal and external audits like customer audit, certification audits, Lead internal product and process audits, Good knowledge of IATF and ISO audits. Required Candidate profile Must be from Automobile industry and preference from Japanese MNC, 1.5yrs to 2years experience in current organization, Ready to relocate near Neemrana / Rewari, Good written and verbal communication.

Creating, implementing, and updating the quality management system, ensuring it aligns with relevant standards (like ISO 9001) and regulations. perform internal/external audits to assess the effectivenes of the QMS and identify areas for improvement. Required Candidate profile Investigating Customer Complaints: They analyze data, identify root causes of quality issues, and implement corrective actions to improve processes and product quality. Can do third party inspection

3.Review Daily Quality inspection reports, Line clearance reports, Final Inspection reports, Certificate of Analysis and ensure Compliance with ISO 9001:2015, ISO 15378:2017, ISO 14001:2015, ISO 45001:2018 & other Customer Standard requirements.

About the Role We are seeking an experienced NetSuite Functional Consultant with strong expertise in manufacturing, supply chain, and advanced inventory processes. The ideal candidate will have hands-on experience in implementing and supporting NetSuites functional modules, including WIP & Routings, Demand Planning, WMS, Advanced Inventory, QMS, and core financials. This role requires a blend of business process knowledge and ERP solutioning skills to drive successful NetSuite implementations and enhancements. Key Responsibilities Lead requirement gathering , fit-gap analysis, and functional design for NetSuite implementations. Configure and support NetSuite Manufacturing modules including WIP & Routings, Work Orders, Bill of Materials, and Outsourced Manufacturing. Set up and optimize Demand Planning and Supply Planning (Material Requirement Planning, Master Production Scheduling). Implement and support Warehouse Management System (WMS) and Advanced Inventory features, including inventory control, replenishment, and costing. Configure and deploy Quality Management System (QMS) within NetSuite for manufacturing quality checks and compliance. Manage core NetSuite configurations: item setup, assembly item configuration, costing methods, order priority, commitment calculations, and reporting. Support customizations and workflow automation , ensuring functional alignment with business processes. Conduct user training, prepare functional documentation, and provide post-implementation support. Collaborate with cross-functional teams to design solutions for SCM and manufacturing challenges. Qualifications Proven experience as a NetSuite Functional Consultant with manufacturing and SCM module implementations. Strong functional knowledge of: Manufacturing (WIP & Routings, Work Orders, BOM, Outsourced Manufacturing) Demand & Supply Planning Advanced Inventory Warehouse Management System (WMS) Quality Management System (QMS) Experience in NetSuite customizations, workflows, and reporting. Understanding of costing methods, supply chain processes, and production scheduling. Excellent communication and documentation skills. Finance background is an advantage. NetSuite certifications preferred. Soft Skills Strong analytical and problem-solving skills. Ability to translate business needs into functional requirements. Client-facing experience with the ability to lead workshops and demos. Role & responsibilities

QMS Standards Knowledge Proficient in ISO 9001, with working knowledge of industry-specific standards such as: ISO 13485 (Medical Devices) IATF 16949 (Automotive) AS9100 (Aerospace) Familiar with global auditing standards and best practices Auditing Conduct internal and external audits, including: ISO audits Supplier and process audits Develop and maintain audit schedules, reports, and corrective action plans Support third-party and certification audits Document Control Manage controlled documents: SOPs, Work Instructions, Quality Manuals, and Forms Maintain document lifecycle through proper version control Ensure compliance with documentation standards and regulatory requirements Corrective and Preventive Actions (CAPA) Perform root cause analysis using methods such as: 5 Whys Ishikawa (Fishbone) Diagrams Initiate, implement, and monitor corrective and preventive actions Track CAPA effectiveness and closure timelines Risk Management Conduct Failure Mode and Effects Analysis (FMEA) Perform risk assessments for products, processes, and system changes Support risk mitigation planning and continuous monitoring Statistical Analysis & Quality Tools Apply Statistical Process Control (SPC) and Measurement System Analysis (MSA) Utilize quality tools such as: Control Charts Pareto Analysis Histograms Scatter Diagrams and Process Capability Process Improvement Methodologies Apply continuous improvement strategies using: Lean Manufacturing Six Sigma (DMAIC methodology) Kaizen principles Conduct value stream mapping and implement waste reduction initiatives Regulatory Compliance Ensure compliance with relevant regulatory frameworks, including: FDA (21 CFR Part 820) CE Marking requirements Good Manufacturing Practices (GMP) Other region/industry-specific regulatory bodies

Oversee the development, implementation, and continuous improvement of the organizations QMS. Ensure compliance with relevant ISO standards (e.g., ISO 9001,14001) and Bureau of Indian Standards (BIS). Required Candidate profile DO NOT CONTACT RECRUITERS DIRECTLY ,APPLY ON NAUKRI AND RECRUITERS WILL GET BACK TO YOU

Oversee the development, implementation, and continuous improvement of the organizations QMS. Ensure compliance with relevant ISO standards (e.g., ISO 9001,14001) and Bureau of Indian Standards (BIS). Required Candidate profile DO NOT CONTACT RECRUITERS DIRECTLY ,APPLY ON NAUKRI AND RECRUITERS WILL GET BACK TO YOU

Oversee the development, implementation, and continuous improvement of the organizations QMS. Ensure compliance with relevant ISO standards (e.g., ISO 9001,14001) and Bureau of Indian Standards (BIS). Required Candidate profile DO NOT CONTACT RECRUITERS DIRECTLY ,APPLY ON NAUKRI AND RECRUITERS WILL GET BACK TO YOU

Oversee the development, implementation, and continuous improvement of the organizations QMS. Ensure compliance with relevant ISO standards (e.g., ISO 9001,14001) and Bureau of Indian Standards (BIS). Required Candidate profile DO NOT CONTACT RECRUITERS DIRECTLY ,APPLY ON NAUKRI AND RECRUITERS WILL GET BACK TO YOU

Oversee the development, implementation, and continuous improvement of the organizations QMS. Ensure compliance with relevant ISO standards (e.g., ISO 9001,14001) and Bureau of Indian Standards (BIS). Required Candidate profile DO NOT CONTACT RECRUITERS DIRECTLY ,APPLY ON NAUKRI AND RECRUITERS WILL GET BACK TO YOU

Oversee the development, implementation, and continuous improvement of the organizations QMS. Ensure compliance with relevant ISO standards (e.g., ISO 9001,14001) and Bureau of Indian Standards (BIS). Required Candidate profile DO NOT CONTACT RECRUITERS DIRECTLY ,APPLY ON NAUKRI AND RECRUITERS WILL GET BACK TO YOU