309 Manufacturing Quality Jobs - Page 7

Quality control and quality assurance oversight Willing to perform inspections personally Inspecting final outgoing products Managing & overseeing PPAP processes Issue analysis & root cause analysis Preparing & updating quality docs

Your future role Take on a new challenge and apply your manufacturing process expertise in a cutting-edge field. Youll work alongside collaborative and innovative teammates. You'll help shape the manufacturing process and ensure its alignment with industrial policies and project constraints. Day-to-day, youll work closely with teams across the business (Engineering, Production, and Quality), develop industrial documentation, and enhance production efficiency through process validation and optimization. Youll specifically take care of defining workstation layouts and performing line balancing, but also support production teams in achieving manufacturing Quality, Cost, and Delivery (QCD) targets. Well look to you for: Gathering and explaining industrial requirements to Engineering during product specification and design phases Designing macro-processes and preparing for the introduction of new technologies Completing industrial documentation, including Industrial Maturity Follow-Up (IMFU) and Process Failure Mode and Effects Analysis (P-FMEA) Validating product design and industrialization through First Article Review (FAR) and First Article Inspection (FAI) Defining and optimizing workstation layouts while adhering to ergonomic and EHS (Environment, Health, and Safety) standards Providing expertise during tender phases and contributing to R&D programs as an industrial representative All about you We value passion and attitude over experience. Thats why we dont expect you to have every single skill. Instead, weve listed some that we think will help you succeed and grow in this role: Technical education Experience or understanding of manufacturing or manufacturing engineering, preferably with 5-10 years in the railway industry Knowledge of process engineering, lean manufacturing, and line balancing Familiarity with ERP systems (such as SAP) and PLM tools (e.g., CATIA, DELMIA) A strong understanding of Quality, EHS standards, and ergonomics Proficiency in English (read, written, and spoken) Good communication, self-motivation, and a logical, organized approach

Job Overview: We are looking for a Quality Control Engineer to ensure in-process and final product quality in a precision manufacturing environment. The role focuses on inspection, documentation, and continuous improvement to meet customer and regulatory standards. Key Responsibilities: Conduct in-process, first-piece, and final inspections. Monitor production quality and adherence to standards. Use statistical tools (e.g., X-Bar charts, Cp/Cpk) for process control. Document inspection results, NCRs, and maintain quality records. Support root cause analysis and corrective actions. Collaborate with cross-functional teams to drive improvements. Ensure compliance with ISO/IATF standards. Requirements: Diploma/B.E./B.Tech in Mechanical or related field. 25 years in quality control (preferably automotive/engineering). Experience in stamping, machining, or heat treatment is a plus. Knowledge of quality tools: 7QC, PPAP, APQP, FMEA, MSA. Strong attention to detail and communication skills

Role & responsibilities We are seeking a Quality Assurance/Process Control professional with hands-on experience in the inspection and monitoring of the manufacturing process in PCBA (Printed Circuit Board Assembly). The candidate will be responsible for incoming goods inspection, in-process and final product inspection, implementation of standards, and process improvements to meet customer requirements. Preferred candidate profile Strong knowledge of PCBA manufacturing and inspection practices as per IPC-A-610 standards. Proficient in preparing, implementing, and sustaining SOPs in the manufacturing environment. Proficient computer skills, including MS Office tools . Familiarity with quality tools and methodologies (FMEA, 5S, 7 QC Tools). Good communication and interdepartmental coordination skills.

Role & responsibilities Must have excellent exposure of handling Customer issues and interacted with customers in day-to-day activities Must have exposure to handle end to end NPD projects Must have exposure to Lead the internal quality audit for system adherence report to management the results and follow up on the corrective actions. Quality Tools implementation like 5S, Quality Circle, Suggestion Scheme, One-piece flow, Kaizen, OEE and VA-VE projects. Knowledge of - 7QC Tools, PDCA, G8D, APQP, PPAP, SPC, MSA Implement best practices, systems and process across CCR operations. Working to collect Warranty, Scrap & re-work data & analysis them for improvement & cost reduction Monthly CTQ parameters data inhouse Responsible for reducing inhouse rejection and rework PPM Process Improvements / upgradation Preferred candidate profile Hands on in Quality functions preferably from Spring or similar product manufacturing Industry

Role & responsibilities Must have excellent exposure of handling Customer issues and interacted with customers in day-to-day activities Must have handled QMS & Audits MR function. Must have exposure to handle end to end NPD projects Must have exposure to Lead the internal quality audit for system adherence report to management the results and follow up on the corrective actions. Managed in house QA activity and reduce customer Quality Complaints. Quality Tools implementation like 5S, Quality Circle, Suggestion Scheme, One-piece flow, Kaizen, OEE and VA-VE projects. Knowledge of - 7QC Tools, PDCA, G8D, APQP, PPAP, SPC, MSA Implement best practices, systems and process across CCR operations. Working to collect Warranty, Scrap & re-work data & analysis them for improvement & cost reduction Monthly CTQ parameters data inhouse Responsible for reducing inhouse rejection and rework PPM Process Improvements / upgradation Preferred candidate profile Hands on in Quality functions preferably from Spring or similar product manufacturing Industry

Review technical documents,specifications,QAP,design drawings etc. to validate design quality,CAPA report Develop and document test standards,test plans,test flow,test procedures,test cases and test results,Inspect electronics to ensure compliance Required Candidate profile Good knowledge of analog and digital electronics Experience in reading design drawings, schematics, technical specifications and determining CTQ Exp in developing test cases and executing/document

The Quality & Compliance Specialist (QA) position at Piramal Pharma Solutions HPAPI Research and Manufacturing facility in Riverview, Michigan requires a dedicated individual to join the Quality Assurance (QA) team. The primary focus of this role is to support the manufacturing operations of the 24x7 facility while ensuring compliance with regulatory standards set forth by the United States Food and Drug Administration (USFDA) and other international authorities. The successful candidate will be responsible for implementing, executing, and maintaining Quality Systems related to manufacturing processes at the PPS-Riverview site. Key responsibilities of the Quality & Compliance Specialist include reviewing batch production records to ensure compliance with Good Manufacturing Process (GMP) requirements, supporting operations by promoting adherence to Good Manufacturing Practices, and carrying out administrative duties such as issuing master production records and maintaining document tracking systems. The Specialist will also be involved in conducting audits, preparing reports, and participating in Quality Systems Metric Reporting and analysis. To qualify for this position, candidates must possess a Bachelor's degree in physical or biological sciences/engineering with at least 1 year of experience in pharmaceutical operations/quality or a related field. Alternatively, an Associates degree with 2 or more years of relevant experience will be considered. Strong knowledge of GMP requirements, proficiency in MS Office, and experience with document management systems are essential for this role. Additionally, excellent organizational, communication, and analytical skills are required to succeed in this position. The successful candidate must be willing to work on a shift-based schedule, including weekends and holidays as needed. The induction period for this role is 3 months, with an expected time to reach performance effectiveness within 6 months. As part of the job conditions, individuals in this role may be exposed to hazardous chemicals and will be required to wear appropriate personal protective equipment. If you are a detail-oriented individual with a strong background in quality assurance and compliance, this role offers an opportunity to contribute to the success of the pharmaceutical manufacturing operations at Piramal Pharma Solutions in Riverview, Michigan.,

A leading manufacturer of industrial packaging products, specializing in BIS-compliant webbing belts and lifting slings, delivering high-quality, safety-focused solutions for logistics, construction, and manufacturing sectors

Career Category Quality Job Description Associate QC QC Systems Templating Role Name: Associate QC Department Name: Quality Control Role GCF: 3 ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world s toughest diseases, and make people s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what s known today. ABOUT THE ROLE Role Description: Let s change the world. Amgen is hiring for a n Associate to support the Electronic Lab Notebook (ELN) and consumable inventory system infrastructure in the Quality Control (QC) network. This candidate will primarily work a shift-based schedule to enable the business in delivering Amgen s mission to serve patients. The candidate may need to work outside of his/her routine workday to support business needs. The individual will be required to work from our office located in Hyderabad India (Amgen India-AIN) and provide remote support from AIN to Amgen sites across multiple time zones globally. Roles & Responsibilities: This position will be responsible for the creation , revision and qualification of template s for analytical method executions in ELN . C reation and revision of consumable templates will also be in the scope of responsibility . The Associate will ensu re assigned tasks are carried out according to the correct procedures, best practices, and service level agreements for QC standardization. Coordination with members within the team at AIN on the same shift and members of the team at AIN on different shifts will be critical in ensuring deliverables are met in accordance with schedule. To effectively provide support, candidates must demonstrate proficiency in virtual communication tools and have experience interacting in remote collaborations. The following are some examples of tasks for the position Creation a n d revision of ELN templates Qualification of ELN templates Creation and revision of consumable templates Understand and follow established instructions to complete assigned deliverables within expectations Collaboration with AIN team members to support the QC network needs Ensuring training is up to date Additional r espon s ibilities may involve: Assistance in providing performance metrics Basic Qualifications and Experience: Master s degree with 1-3 years of Pharma and Biotech commercial or clinical manufacturing Quality Control experience. Functional Skills: QC lab testing experience Exposure to ELN a pplications Microsoft Office proficiency Familiarity with Good Manufacturing Practices and Good Documentation Practices Soft Skills: Excellent English verbal and written communication skills Ability to learn quickly with attention to detail Delivering results right first time within a team environment EQUAL OPPORTUNITY STATEMENT We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation . .

To head and manage Quality function across Suppliers, Processes and Customers. Will handle Quality Assurance Strategy for Supplier / Manufacturing value chain for continuous improvement of Overall Quality Metrics etc.

Job Title: Quality Engineer Aerospace & Defence Location: Dasna, Eastern Peripheral Highway, Ghaziabad Experience: 6 to 8 years in a manufacturing setup Education: B.Tech/B.E. Electrical / Production / Aerospace (Only from IIT/NIT) Role Summary: We are seeking a sharp, committed, and mission-driven Quality Engineer to ensure that our high-precision components and systems meet the rigorous standards of the aerospace and defence sector. The ideal candidate is tough-minded, meticulous, and driven by purpose . Key Responsibilities: Implement and monitor quality control processes , non-conformance handling , and root cause analysis . Maintain compliance with ISO 9001 , AS9100 , and defence-specific quality standards. Work with cross-functional teams for first article inspection , in-process inspection , and final product validation . Develop and maintain detailed quality documentation , control plans, and inspection reports. Drive continuous improvement initiatives using Six Sigma, 5S, and Lean methodologies. Requirements: Engineering degree from IIT/NIT with 6 to 8 years of relevant experience. Prior experience in precision manufacturing , defence , or aerospace components is highly preferred. Strong analytical skills, attention to detail, and the ability to work under pressure. Passion for discipline, quality excellence, and impact .

DME / B.E - Mechanical Min 2+ yrs of expn in Quality Engineer in any Automobile / Forging Industry etc Good knowlege in Final Quality Inspection Job Location : Chennai Only Food will be provided.

We are looking for a dynamic and experienced Quality Assurance Lead to control quality processes at our manufacturing unit in Bangalore. The role involves overseeing daily QA activities, conducting audits, ensuring compliance in quality systems.

Evaluate potential product quality complaints and initiate applicable records and actions within proper Quality System. Own and process quality complaint as per applicable procedures. Determine, facilitate and/or approves reportability assessments and decisions based on applicable procedures. Author and submit applicable regulatory reports (MDR, MIR, etc.) to competent authorities when deemed required. Monitor the status and progression of complaints under investigation and initiate actions to facilitate its resolution and closure. Review and approve the results of Engineering, Manufacturing, Quality, Service and/or Supplier evaluations and investigations of complaints. Performs queries to provide complaint data and ad hoc trend analysis on reported product problems/complaints to drive continuous improvements within the department and organization. Performs other duties as needed and assigned.

The QA & QC Head will be responsible for coordinating all activities necessary to direct and control manufacturing quality. This includes reviewing product quality requirements for individual clients and projects to ensure thorough understanding and implementation. The main focus will be on managing the quality of manufactured items to meet the contract specifications. The ideal candidate should have at least 5 years of experience in the Medical Device Field. The position is located in Metoda G.I.D.C., Rajkot. Salary will be commensurate with experience.,

design quality, supplier quality, manufacturing quality and field quality, CTQ in respective areas of ODM operation, Ensure product & process approbations, Overall MR for ISO related certifications, IS & IEC quality standards for lighting products,

Preferred Education/ Qualification : B. Pharm/M. Pharm/M. Sc. Experience : 6 8 years of experience in Quality Assurance / MQA of sterile dosage manufacturing facility /Technology Transfer/Validation. Core Competencies : Technology Transfer of injectables Change Management process Risk assessments principles and tools Validation of manufacturing equipment s Drug Product Process validations Regulatory requirements Compendial Changes Technical Skills : Fundamental knowledge on manufacturing and Quality control activities, such as Solution preparation, filling, terminal sterilization, visual inspection, packing, in process sampling and analysis. Technical document review skills Knowledge in change control assessment Knowledge on manufacturing process such as stopper processing, sampling and dispensing, solution preparation, Component Preparation, Filling and Capping of Drug Product. Should be capable of handling regulatory inspections USFDA/MHRA/TGA, etc. , Behavioural/ Any Other Skills: Interpersonal Skills: Effective communication with all staff from different levels and builds constructive and effective relationship Acts Decisively: Makes decision in a timely manner based on available information Grows Self: Identify Individual development needs and create a plan and work towards achieving those objectives Critical thinking and Compliance mindset. Core Responsibilities : Good performance, partially independent, reviews trends and data Responsible for review of Manufacturing documents such as SOPs, Process validation, cleaning validation, cleaning process verification documents, Batch manufacturing records, Exhibit batch plan, Exhibit batch Summary Reports. study protocols and reports. Tracking of change controls, Providing QA Impact Assessment, preapproval, post approval & closure of action items. Coordinating with CFT for addressing & resolving of Review Comments for timely Closure. Review of product & process related SOP, Job aids & Forms. Review and approval of NVPC, PH and conductivity. Review and approval of APQR s. Report any non-compliance to the Supervisor Should have trouble shooting abilities in manufacturing Quality area, which helps the organization to develop, implement and achieve its mission, vision and values. Identify gaps and involve in process and procedure simplification, thereby reduce downtime and increase the Efficiency. Experience in handling regulatory, corporate and internal auditors/ inspectors. Work Location Assignment: On Premise Quality Assurance and Control #LI-PFE

Role & responsibilities : Candidate is responsible for 5 Star Audit IATF Audit Quality Core Tools New Project Development Business plan Preparation Customer Handling (QC, QA & SQA) APQP, PPAP, FMEA , Control Plan, SPC, MSA, IATF Documentation Product Development, Supplier Sourcing, VAVE / Cost Savings, Project Management QC Tools - Pareto & why why analysis Process Improvements, Problem solving, Internal Audit, Process Audit / Product Audit Supplier Evaluation, Performance Monitoring, CAPA Analysis Examine the Monthly Quality Results and developments, Reporting to Management Make ensuring that all the Customer Specific Requirements are met.

Role & responsibilities Position Summary To drive the successful transformation of the business in becoming a world-class sourcing organization by providing technical garment/apparel expertise and recommendations to vendors/factories and internal sourcing teams. To develop and drive the implementation of new apparel technical programs across the region. Key Accountabilities: Networks with vendors/factories and the Sourcing/Merchandising teams to conduct a preliminary inspection on the products at the pre-production stage Participates in Pre-Production Meetings to review Tech. Packs and Ticketing Reports Good prevention, problem solving skill; a solution provider Skills in risk assessment, factory evaluation and effective CAP follow-up to help factory improve their system Provide answers to queries from colleagues and vendors in professional manner, and conducts follow-up work promptly Addresses any issues promptly pertaining to product safety, engineering or technology and prevents confirmation of bulk production Supports the departments change of focus from Quality Control to Quality Engineering and Product Technology Conducts factory visits to provide guidance and counseling as required Diligently conducts follow-ups with factory production supervisors to check on the status of corrective action Promptly advises necessary Product Technology & Quality Assurance colleagues of any suspected non-compliances with vendors/factories Conducts factory inspection visits to review the standards of the operation, and take necessary action to ensure product safety, quality and compliance of our products at the production factory Identifies training opportunities for vendors, factories and colleagues Conducts relevant workshops and seminars on product inspection Participates in relevant industry training in Product Technology, Safety Quality Assurance, and Regulatory Compliance Education and Experience: At least 2 years working experience in Apparel Industry: Manufacturing, Product Technology, Quality Assurance, Product Inspection, Factory Audit, or similar field Related education or training experience Comprehensive background in factory or apparel inspection Comprehensive knowledge of Product Technology and Safety Standards for children’s apparel Ability to quickly identify production, product technology, or product safety problem areas and quickly recommend solutions Proficiency in Microsoft Office applications (Word, Excel, PowerPoint and Outlook) Good command of both verbal and written English and local language Possess a strong attention to detail and time management Behavioral Competencies: Drives Business Results through Communication and Collaboration Plans and Organizes Exhibits and Drives Accountability Is an effective team member

Role & responsibilities Position Summary To drive the successful transformation of the business in becoming a world-class sourcing organization by providing technical garment/apparel expertise and recommendations to vendors/factories and internal sourcing teams. To develop and drive the implementation of new apparel technical programs across the region. Key Accountabilities: Networks with vendors/factories and the Sourcing/Merchandising teams to conduct a preliminary inspection on the products at the pre-production stage Participates in Pre-Production Meetings to review Tech. Packs and Ticketing Reports Good prevention, problem solving skill; a solution provider Skills in risk assessment, factory evaluation and effective CAP follow-up to help factory improve their system Provide answers to queries from colleagues and vendors in professional manner, and conducts follow-up work promptly Addresses any issues promptly pertaining to product safety, engineering or technology and prevents confirmation of bulk production Supports the departments change of focus from Quality Control to Quality Engineering and Product Technology Conducts factory visits to provide guidance and counseling as required Diligently conducts follow-ups with factory production supervisors to check on the status of corrective action Promptly advises necessary Product Technology & Quality Assurance colleagues of any suspected non-compliances with vendors/factories Conducts factory inspection visits to review the standards of the operation, and take necessary action to ensure product safety, quality and compliance of our products at the production factory Identifies training opportunities for vendors, factories and colleagues Conducts relevant workshops and seminars on product inspection Participates in relevant industry training in Product Technology, Safety Quality Assurance, and Regulatory Compliance Education and Experience: At least 2 years working experience in Apparel Industry: Manufacturing, Product Technology, Quality Assurance, Product Inspection, Factory Audit, or similar field Related education or training experience Comprehensive background in factory or apparel inspection Comprehensive knowledge of Product Technology and Safety Standards for children’s apparel Ability to quickly identify production, product technology, or product safety problem areas and quickly recommend solutions Proficiency in Microsoft Office applications (Word, Excel, PowerPoint and Outlook) Good command of both verbal and written English and local language Possess a strong attention to detail and time management Behavioral Competencies: Drives Business Results through Communication and Collaboration Plans and Organizes Exhibits and Drives Accountability Is an effective team member

for a manufactured material, component, or product. Building and maintaining the infrastructure and systems necessary to consistently ensure the timely delivery of quality products. Auditing, monitoring, and determining the quality of manufacturing processes and/or outputs against defined internal and regulatory standards. Reporting and troubleshooting manufacturing process deviations and defects in finished goods An Experienced Professional (P2) applies practical knowledge of job area typically obtained through advanced education and work experience. May require the following proficiency: Works independently with general supervision. Problems faced are difficult but typically not complex. May influence others within the job area through explanation of facts, policies and practices. How you ll make an impact Support related management systems in quality function like ISO14001:2015 & ISO45001:2018. Coordination of customer audit & follow up the actions. Planning and Performing Quality Management System Audits, Global Quality Assessment & Customer Audits. Follow up of NCRs & Coordinate Root Cause Analysis (8D etc.) and define the action w/ related team which come from internal audits, customer audits, during manufacturing or customer claims (CCRP). Responsible to define Inspection Test Plans (ITP) based on contracts & relevant standards. Coordinate the functional tests w/ customer & prepare the relevant report for Final Acceptance Report (FTA). Close cooperating with other functions in Hitachi Energy (Production, SCM, R&D, Engineering etc.). Increasing supplier quality awareness and drive Zero Defect mentality within the supply base. Lead & Support Supplier in terms of quality training problem solving methods etc. instruction & control form preparation etc. Coordinate improvement projects which are derived from Cost of Poor Quality & NCRs. Supporting initiatives and audits launched by Group function / Division on Sustainability, Material compliance, Integrity and Health, Environment and Safety. Coordinate Computer Aided Quality Projects. Support defined improvement projects. Living Hitachi Energy s core values of safety and integrity, which means taking responsibility for your own actions while caring for your colleagues and the business. Responsible to ensure compliance with applicable external and internal regulations, procedures, and guidelines. Your background Bachelors degree in electrical/mechanical engineering At least 2 years of professional experience in quality Preferred knowledge and experience in power transformer industry Practical Knowledge of SAP QM. Technical knowledge of relevant products pertaining to the power T&D industry. High Voltage Test Laboratory knowledge is an advantage. Practical knowledge in implementation of Lean production and Six Sigma, technical knowledge for supplier qualification, material and production processes. Valid driving license. No restriction for travelling. Proficiency in both spoken & written English language is required. .

Role & responsibilities Lead and manage the Quality function and teams across the plant. Lead Incoming Quality Control (IQC), In-Process Quality Control (IPQC), and Outgoing Quality Control (OQC) to ensure product conformance for regular and new products. Oversee the deployment and optimization of Inspection Activities. Oversee in-house calibration activities for instruments and gauges. Analyse quality data using advanced analytical tools (e.g. SPC, DOE, FMEA, and Root Cause Analysis). Support PPAP, FMEA, SPC, Product, Process & System audits. Develop, implement, and manage the Quality Management System (QMS) to meet company and industry standards. Design and support to make SOPs and Work Instructions for processes and operations. Handle customer concerns and claims, ensuring timely resolution and root cause analysis. Monitor and improve KPIs to ensure compliance with quality standards and efficiency goals. Leadership & Strategy - Develop and implement quality strategies aligned with customer requirement. Lead a team of QC engineers and inspectors. Act as the point of contact for all customer quality concerns and audits. Documentation & Reporting - Maintain quality documentation per QMS requirements. Track and report quality KPIs: PPM, rejection %, rework %, audit scores, etc. 7 QC tools and CAPA/critical analysis of process and product to improve the quality. Lead continuous improvement initiatives such as Lean, Six Sigma, and Kaizen to enhance product quality and reduce process variation. Analytical Requirements: 1. Data-Driven Decision Making Using quality metrics, SPC, and audit findings to guide improvements. 2. Corrective & Preventive Action (CAPA) – Identifying root causes and ensuring long-term solutions. 3. Trend Analysis & Reporting – Monitoring feedback, complaints, and quality KPIs for improvement insights. 4. Risk Assessment – Assessing potential risks in materials, suppliers, and internal processes.

Min 15 years of exp in Auto industry with atleast 3 to 4 years exp in Automotive / Sheet metal industry Familiar with TQM principles, iso 9001,iso 14001,TS process knowledge like Machining, CNC, VMC, Turning, grinding etc Able to handle OEM audits Required Candidate profile Candidate must be B.tech with atleast 15 years experience of handling Quality Assurance Handling customer audits, Working on rejection & rewor. Candidate must have excellent communication skills.

Greetings from Manpower Resources India (P) ltd. Manpower Resources India Pvt. Ltd is a leading Executive Search & Selection company, caters to recruitment services in Manufacturing, Infrastructure, Engineering & Healthcare domain. We have been mandated by a large conglomerate into Stainless Steel Manufacture. Position Title: Quality head -DGM/Sr. Manager Department: Quality Assurance & Quality Control Location: Boisar, Tarapur, Maharashtra Industry: Stainless Steel Seamless Pipe Manufacturing Experience: 10-15 Years of relevant experience. Qualification: BE / Diploma -Metallurgist /Mechanical Purpose of the Role: To ensure the quality of stainless-steel seamless pipes produced in the plant by conducting inspections, tests, and audits at various stages of production, ensuring compliance with national and international standards, customer specifications, and internal quality norms. Role & Responsibilities: Sound knowledge of Stainless-steel seamless pipe grades. Strong analytical and problem-solving abilities. Good communication skill for effective coordination. Knowledge of SAP. To ensure that quality of stainless-steel seamless pipes meet international standard & as per customer specification by conducting the process audits, Strong hold on shop floor management. Ensuring adherence to SOPs, QAPs ,and applicable ASTM ,EN , IS and other applicable standards Responsible for the shop floor inspection activities and NDE . Controlling the all 3 shifts inspection output and manpower with inspection records. Responsible for maintain the NCRs and deviation reports & records. Log the non-conformity with proper root cause analysis and initiate corrective actions in consultation with production and quality leads. Responsible for timely coordination with the in-house mechanical and chemical lab for applicable testing & its reports. Attend Quality issue with supplier plant. Support implementation of Six sigma, 5s, lean practices on shop floor. Responsible for all kind of shop floor activities. Responsible for Clearance of the non-Confirmed materials as per norms from the quality to designated area or department. Responsible for Daily inspection against target, and salvaging rework and rejection as per quality norms.