89 Ipqc Jobs

Responsibilities: * Conduct IPQC, FGQC, quality inspections * Ensure compliance with GMP & BMR guidelines * Implement CAPAs and QMS procedures * Manage raw material inspections * Perform microbial analyses Office cab/shuttle

Lead and manage group of QC technicians and testing engineers, offering direction, instruction, and performance evaluation to guarantee high-quality output Testing and troubleshooting of PCBs and electrical/electronic panels Required Candidate profile DO NOT CONTACT RECRUITERS DIRECTLY ,APPLY ON NAUKRI AND RECRUITERS WILL GET BACK TO YOU

Job Title Lead Engineer QC Paint Shop Functional Scope Hands on experience in In-process Quality Responsibilities - First piece & In-process inspection review and approval - Process Validation for spray paint, pad printing and digital printing - Process and Product Audit - Daily rejection review and action plan tracking - Involvement during new product development w.r.t painting process - Handling of non-conforming product - Fixture, Jig, and Mask validation per defined plan - SAP clearance on daily basis for accepted/rejected lots - Hourly defect monitoring on the line and actions in case of abnormal results - Chemical Management, Sharp tool management & Traceability per customer and internal QMS requirements - Paint/Ink/Thinner Self life monitoring and re-validation of expired materials - Weekly/Monthly data update and report to management with detail analysis - Root cause analysis and action plan for the defects identified at paint shop and internal customer. - Continual improvements Skill Sets - Paint shop/Deco background must - Chemical management & Problem-solving tools. - Experience in plastic industry background added advantage. - ISO 9001 QMS & Working experience with Hasbro customer added advantage. Experience - B.E (Mech) with 6 - 8 years of experience OR Diploma (Mech) with 8-10 years of experience in a manufacturing organization - Minimum 3 years experience in IPQC and Paint shop experience must Job Location Koppal, Karnataka, India.

As a member of the Group Company's Capsules team, your primary responsibilities will include checking the allocated post production (ATS/Printing/camera) line(s) in each shift according to the CTQ (critical to Quality) / CTP (Critical to Productivity) checklist. You will be required to follow the plan for color change noted, ensuring minimal change over time at each subsection. It is essential to follow instructions from the shift lead to facilitate timely changeover by ensuring the availability of rollers/ink, etc. You will execute IPQC after every roller cleaning, checking rejections of cameras every hour to achieve zero defects. Operating cameras as per SOP to meet productivity and quality standards is crucial. Collaboration with contract associates to ensure SOP compliance at ATS/Camera/packing/Sealing and tumbling is part of your responsibilities. It is imperative to implement the preventive maintenance plan for the line(s) to achieve zero downtime and execute troubleshooting activities to maintain productivity, seeking maintenance team support when necessary. Reporting and controlling post-production loss of printing and camera to achieve the targeted AFOE@Despatch, as well as following cGMP and GDP for the allocated line(s) to ensure regulatory compliance during the shift, are essential tasks. Moreover, you must adhere to instructions from the shift lead/team lead to implement CAPA for any customer complaints. Your key result areas will involve maintaining line continuity, productivity, product quality, reducing wastage, and adhering to cGMP, GDP, and safety regulations during the shift for the allocated line(s). Key Interfaces: - Productivity of the line - Print loss/print reject/camera loss - Safety - SOP Adherence Competencies: [Competencies not provided in the input],

Lead and manage group of QC technicians and testing engineers, offering direction, instruction, and performance evaluation to guarantee high-quality output Testing and troubleshooting of PCBs and electrical/electronic panels IPC610, QAP, Type Testing Required Candidate profile Create and implement quality control methods and practices for PCB testing and electrical/electronic panels, making sure they comply with industry norms, client demands, and legal requirements

Hands on experience in Quality Management of Power Electronics Products like Lithium Ion battery pack, BMS, Lithium ion charger, UPS, Inverters, SMPS (AC-DC/ DC-DC) etc., Should have thorough Knowledge in all types of Communication circuit design like, CAN, MODBUS, USB, GPRS/GSM, WIFI, NFC, BLE etc., Should have knowledge about various EMI/EMC / Safety compliance standards as per IEC / EN /UL etc., Knowledge about Reliability Testing and methods. Knowledge about battery pack line, laser welding, ultrasonic welding, soldering and other welding process related to lithium ion battery manufacturing process. Having depth knowledge of cell shorting, cell grouping, cell testing, battery testing & other testing related to lithium ion battery. Having knowledge of Lithium ion battery cells Pouch/Cylindrical/Prismatic, NMC/LFP cells. Responsible for Failure analysis with CFT Ensure process adherence to meet product quality Ensure report management like RCA of the product Daily FPY, 4M change tracking Familiar with FMEA, Control plan, MSA, SPC,8D,7 QC Tools On time rejections clearance physically / system wise. Should be familiar with any one ERP /SAP/MES Should be familiar with Li-Ion Battery manufacturing / Electronics industries Responsible for TQM department functions Responsible for failures RCA & PCA

Hands on experience in Quality Management of Power Electronics Products like Lithium Ion battery pack, BMS, Lithium ion charger, UPS, Inverters, SMPS (AC-DC/ DC-DC) etc., Should have thorough Knowledge in all types of Communication circuit design like, CAN, MODBUS, USB, GPRS/GSM, WIFI, NFC, BLE etc., Should have knowledge about various EMI/EMC / Safety compliance standards as per IEC / EN /UL etc., Knowledge about Reliability Testing and methods. Knowledge about battery pack line, laser welding, ultrasonic welding, soldering and other welding process related to lithium ion battery manufacturing process. Having depth knowledge of cell shorting, cell grouping, cell testing, battery testing & other testing related to lithium ion battery. Having knowledge of Lithium ion battery cells Pouch/Cylindrical/Prismatic, NMC/LFP cells. Responsible for Failure analysis with CFT Ensure process adherence to meet product quality Ensure report management like RCA of the product Daily FPY, 4M change tracking Familiar with FMEA, Control plan, MSA, SPC,8D,7 QC Tools On time rejections clearance physically / system wise. Should be familiar with any one ERP /SAP/MES Should be familiar with Li-Ion Battery manufacturing / Electronics industries Responsible for TQM department functions Responsible for failures RCA & PCA

They are involved in planning and implementing strategies for quality management and testing. Plan, conduct and monitor testing and inspection of materials and products to ensure quality Review the implementation and efficiency of quality and inspection system Monthly monitoring the quality Rating Document internal audits and other quality assurance activities and Evaluate audit findings and implement appropriate corrective actions Motivate and lead the team for continuous improvement in the quality process Ensure right quality of all components from vendor. Modify design to increase product performance and assembly time Develop, manage implement, communicate and maintain a quality plan to bring the Company's Quality Assurance Systems and Policies into compliance with quality system requirements. Effectively interact with Technical, Development and Production team to maintain product quality; ensuring that targets are achieved. Assisting technicians with checking patterns/specification and construction, identifying and resolving production impracticality in an appropriately timely manner, and to make a final decision on quality according to company standards and requirements. Role & responsibilities IQC (Incoming Quality Control) IPQC (In process Quality Control) FQC (Final Quality Control) Preferred candidate profile

Knowledge of Daily Line Problem solving and having knowledge of Gear Manufacturing Process. Knowledge of implementation of core tool to resolve daily reporting issue on line. Capture process gap and data compilation of QA department. Required Candidate profile CANDIDATES FROM GEARS MANUFACTURING INDUSTRIES ONLY. EXPERIENCE IN IN PROCESS QUALITY. Data analysis & prepare technical presentation for customers and management. Coordination Inter Department.

Roles and Responsibilities Conduct quality audits, inspections, and testing of electrical panels, control panels, switchgear products to ensure compliance with IEC standards and ISO 9001:2015. Develop and implement quality plans, procedures, and SOPs for incoming quality control (IQC), internal process quality control (IPQC), final product inspection (FQI), and supplier quality assurance. Perform root cause analysis (RCA) investigations on defective products or non-conformities using tools like 7 QC Tools. Collaborate with cross-functional teams to identify areas for improvement through kaizen events and implement corrective actions through CAPAs. Ensure timely completion of NCR reports and follow up on pending issues related to quality. Desired Candidate Profile Strong understanding of IEC standards and IS codes; knowledge of ISO 9001:2015 is essential. Proficiency in preparing Inspection Reports, SOPs, Quality Plans, RCA reports; ability to conduct panel testing (HV). Excellent communication skills with ability to work effectively with vendors; proficiency in MS Office applications. min. 3 years' experience in the switchgear industry.

Job Title: Quality Assurance Officers (4 Positions) Company: Nourish Pharmaceutical Pvt Ltd Location: Kheda, Gujarat Job Type: Full-time Nourish Pharmaceutical Pvt Ltd is a leading pharmaceutical company committed to delivering high-quality products. We're expanding our Quality Assurance team and looking for talented professionals to join us. Positions: 1. Quality Assurance Officer - Production 2. Quality Assurance Officer - QMS 3. Quality Assurance Officer - Validation & Qualification 4. Quality Assurance Document Control Officer Job Descriptions: 1. Quality Assurance Officer - Production - Key Responsibilities: - Ensure cGMP compliance in production areas - Manage and review Batch Manufacturing Records (BMRs), Batch Packaging Records (BPRs), and Master Formula Records (MFRs) in Pharma Cloud - Conduct in-process quality checks and documentation - Verify dispensing activities and line clearance - Collaborate with production team to ensure quality and compliance - Core Skills: - Attention to detail and analytical skills - Strong knowledge of cGMP, SOPs, and quality control procedures - Excellent communication and interpersonal skills - Experience & Qualification: - 0-3 years of experience in a similar role within the pharmaceutical industry - B.Pharm or M.Pharm degree in Pharmacy or a related field - Certification in quality assurance or a related field is an added advantage 2. Quality Assurance Officer - QMS - Key Responsibilities: - Manage deviations, CAPAs, and document handling - Ensure compliance with Quality Management System (QMS) standards - Conduct internal audits and facilitate external audits - Review and update SOPs, policies, and procedures - Collaborate with departments to ensure quality and compliance - Core Skills: - Strong analytical and problem-solving skills - Excellent communication and interpersonal skills - Ability to work independently and prioritize tasks - Experience & Qualification: - 1-3 years of experience in a similar role within the pharmaceutical industry - B.Pharm or M.Pharm degree in Pharmacy or a related field - Certification in quality assurance or a related field is an added advantage 3. Quality Assurance Officer - Validation & Qualification - Key Responsibilities: - Plan, coordinate, and execute validation and qualification activities - Ensure compliance with validation and qualification protocols - Review and approve validation reports and documentation - Collaborate with departments to ensure quality and compliance - Identify and mitigate risks associated with validation and qualification - Core Skills: - Strong knowledge of validation and qualification procedures - Excellent analytical and problem-solving skills - Ability to work independently and prioritize tasks - Experience & Qualification: - 1-5 years of experience in a similar role within the pharmaceutical industry - B.Pharm or M.Pharm degree in Pharmacy or a related field - Certification in validation and qualification or a related field is an added advantage 4. Quality Assurance Document Control Officer - Key Responsibilities: - Manage and maintain document control system - Implement and maintain change control system - Issue and maintain logbooks and records - Ensure plant and product documentation is accurate and compliant - Collaborate with QA team to ensure document accuracy and compliance - Core Skills: - Attention to detail and organizational skills - Basic knowledge of cGMP and quality control procedures - Excellent communication and interpersonal skills - Experience & Qualification: - 0-2 years of experience in a similar role within the pharmaceutical industry - B.Pharm, B.Sc or M.Pharm degree in Pharmacy or a related field - Certification in validation and qualification or a related field is an added advantage - All positions open for Fresher B.Pharm or M.Pharm degree in Pharmacy, Willingness to learn and grow in a quality assurance role How to Apply: If you're a motivated and detail-oriented individual with a passion for quality assurance, please submit your resume to info@nourishpharma.com

Role & responsibilities We are looking for a detail-oriented IPQC Officer to monitor and control product quality during the manufacturing process. The candidate will ensure that production processes meet the required quality standards, perform inspections at various stages, and support continuous improvement initiatives. Line Clearance before the start of the Production activities. Conduct in-process inspections and quality checks at different stages of production. Identify and report any deviations, non-conformities, or quality issues to the production. Record and maintain in-process inspection data accurately. Ensure proper implementation of Good Manufacturing Practices (GMP) and Standard Operating Procedures. Collaborate with production teams to resolve quality-related issues in real time. Assist in root cause analysis and corrective/preventive actions (CAPA). Support internal and external quality audits and inspections. Ensure compliance with ISO, GMP, or industry-specific quality standards. Monitor critical parameters as per Standard Operating Procedures (SOPs) and quality guidelines. Preferred candidate profile Knowledge of quality assurance and in-process inspection techniques. Familiarity with instruments like vernier calipers, micrometers, or other testing equipment. Excellent Communication skills Attention to detail and problem-solving abilities Ability to work independently and as part of a team

Followings will be the core job responsibilities of the position holder: 1. Responsible for Operation, cleaning, and primary maintenance of compression machine, metal detector, Lifting and positioning device, IPQC instrument. 2. Responsible for recording of activity in logbooks, Batch manufacturing record & Responsible for complete documentation as required in the manufacturing of product and the cleaning of facilities and equipment, following cGMP s and good documentation practices. 3. To Ensure Area and equipment cleaning before line clearance as per standard procedures. 4. To perform all in-process checks and monitoring of all intermediate processes in compression. stage. To select recipes and set process parameters in PLC/SCADA compression ,IPQC instruments HMI & ensure its correctness before blender revolution. 5. Responsible for Issuance, utilization, cleaning, and retrieval of tooling s and machine change parts with its inventory. 6. Responsible for set up, changeover, and operation of various manufacturing equipment s but not limited to compression area. 7. Responsible for reporting and/or escalating any conditions or problems that may affect the quality or integrity of product to supervisor and HOD production. 8. Responsible for maintaining a neat, clean and safe working environment always and notifies supervisor immediately if any safety concerns, accidents or injuries are observed. 9. To ensure all in-process checks and monitoring of all intermediate processes, to check set process parameters in PLC/SCADA as per BMR before machine run in compression area. 10. Compliance of current Good Manufacturing Practices in the Hormone Facility & to follow GDP with data-integrity compliance. 11. To Complete the training and training record as per stipulated time. 12. Responsible for preparation and usage of Disinfectant and cleaning agent solution as per defined procedures. 13. To adhere to all Company policies, procedures, SOPs and Safety regulations. 14. To do overtime as needed & responsible for performing additional task, related duties as assigned.

JOB DESCRIPTION 1. JOB DESCRIPTION SUMMARY Handling system requirements as per ISO 9001 and SA 8000(CSR). Prepare Audit Plan for Internal System Audits (QPA, ISO 9001, SA8000 (CSR)) & conducting audit as per audit plan with closure of NC's observed during the audit. Prepare Supplier Audit plan & conduction supplier audits as per plan and follow up with supplier to close all NCs observed during audit. Handling customer audits conducted in JTI and closing NCs observed during customer audit. Review product quality standards as per customer requirements/standard from time to time. Review CTQ checkpoints identified & maintained properly from time to time. Ensure production process is followed as per defined SOP and WI by conducting audits from time to time. Establish, review and update system audit checksheet as per system requirements. Establish, review and update system manuals from time to time. Establish, review and update procedures as per requirement and provide support to all departments in implementing the same. Identify potential areas for continual improvement and maintain records of improvements projects which are identified, under process and concluded successfully. Identification of risk & opportunities and providing proper control over identified risks which are considered unacceptable/High risks during risk analysis from time to time. Communicate with department heads, managers, and employees to discuss audit findings and recommendations. Present the results of completed audits to management, highlighting key findings and suggesting improvements. Track the implementation of audit recommendations made in previous audits. Verification of corrective actions provided against NCs observed during the audit with monitoring of effectiveness monitoring against the problem observed. Follow up on the implementation of recommendations from previous audits to assess progress. Establish, review and update Environmental inspection (RoHS) XRF process defined complying with customer as well as global standards(QC080000)

Position: R&D OFFICER Education: BSc. in chemistry, MSc. in chemistry or B.pharma / M.Pharma Experience: minimum 10 year in API pharmaceutical industries. Salary: 50 to 70 K per month Mo No : +91 90816 99400 / +91 90816 88100 / 90816 99600 Required Candidate profile Coordinate with regulatory authorities for inspections, licensing, and compliance documentation. Investigate quality incidents, deviations, and complaints, ensuring timely resolutions

Responsibilities include production operations, equipment handling, cleaning, maintenance, QA/validation support, & GMP compliance. Must follow SOPs, ensure timely activities, & reports. Male candidates only. Understand the role before applying.

Job role: Lead Mechanical Engineer Job Location: Bangalore Only EXP: 7 - 15 + Years (Mechanical engineer Background) Gender: Male Only Department: Build - Mechanical Reports to: Build - Head/ Manager Job Summary: We are seeking a dynamic and technically strong Lead Member Industrial Automation & Mechanical Systems to lead and execute end-to-end automation projects involving Machine Assembly, Machine Maintenance, fat, sat, IQC, IPQC, machine testing, machine installation. The ideal candidate will have hands-on experience in diverse industrial environments, including steel plants, CNC machines, robotic systems, and crane automation. Getting work/assemblies done from Contract Resource & Members as per drawings as per the plan in consultation with superiors. Generate the build, Testing, Dispatch & I&C documents. Roles & Responsibilities: Plan and track allocated Project plan Monitor and track the allocated team member's output Coordination with internal Department for in time Project Execution at plant and site Follow and maintain the Departmental Process. In time escalation for issue to complete the work in time Action on issues raised by team members Maintain the quality and quantity in machine building activity. Test the machine as per SOP Tear down and packing plan and execution. Maintain and improve the Build and testing process Create RCA and 8d Report for Major issues Maintain the safety and 5s at working area Proper Utilization train the allocated Temporary resources Create RCA for Major issues Team Technical and Personal Development Process Development to reduce effort Proper Full kit Preparation like Manpower/Material/Method and proper preservation of tools and record Process and tool development to eliminate waste (Time, Material) Departmental Budget Control Required Education qualification: Diploma/BE (Mechanical/Production/Mechatronics) Contact : Jeevarathinam : +91- 8608666969 Fayas: +91-8754911487 Mail Id: jeevarathinam.s@wipropari.com fayas.k@wipropari.com

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

ARKRAY Healthcare Pvt. Ltd. Surat, India Document Control OP/F/046, Ver. 01, Effective date: 01.09.2022, Due date: 31.08.2027 Job Description (Reference Procedure: OP/S/001) JD No. JD-QLT-022Organization Level Division / Department / Team / Supervisor / Team MemberJob TitleExecutive ILJob PurposeCarries out monthly testing of finished products of serology & microbiology products and manage Quality Control Activity in Arkray Healthcare Pvt Ltd. Job ImportanceDay to day observation of test for sterility and recoding the same.Job Responsibilities Ensuring that all raw materials (ROH), packing materials (VERP) are tested in time (as per TAT) and release as per the approved quality specs/documents. Ensuring that all the in process (IPQC) and semi-finished products (HALB) are tested in time (as per TAT) and release as per the approved quality specs/documents. Ensuring that all the finished products (FERT) are tested in time (as per TAT) and release as per the approved quality specs/documents. Ensuring periodic conduction of calibration, testing and measuring instruments/equipment as per schedule in the section. Prepare and standardize the lab use reagents. Assisting Asst. Manager/Section Head in adherence to the regulatory and FDA audit process (internal and external). Ensuring for timely completion of different types of stability (Real Time, Accelerated Transport Stability/In use Stability) for various stages of materials/reagents/finished product in the section. Assisting Asst. Manager/Section Head for new vendor or alternative vendor development activity in the section. Ensuring of QC area (cold rooms, deep freezers, incubators, laboratory) as per GMP compliance. Ensuring records are filled properly, stored properly and easily retrievable. Assisting Manager QC/Asst. Manager/Section Head for microbiology work like sterility test and work related to prepare before sterility test. Identification of organisms. All other activities as and when required by superior. Job Authority Authorized to do Various Types of sampling, Testing and Releasing (ROH / VEPR / INP / HALB / FERT / HAWA) as per std. TAT (SQ/TR/023). Authorized to do Lab use Reagent / Buffer preparation (SQ/TR/026). Authorized to use Different Types Incubators / Oven / Water Bath and Freezers Handling (SQ/TR/028). Review of plan, protocol and report of study conducted by QC. Candidate Requirements Should have good knowledge about product. Good communication skills verbal as well as written. Good Team Player with proactive approach and experience of working in Cross Functional Teams (CFT). LocationARKRAY Healthcare Pvt. Ltd. Plot No. 336-338-340, Road No. 3, GIDC- Sachin, Surat- 394 230, Gujarat, IndiaTravelling RequirementsNo QualificationM.Sc / B.Sc (Prepared By) HRGA Team Manager (Reviewed By) Reporting Manager (Approved By) HRGA Department ManagerNameShaligram DodiaRajesh PancholiShaligram DodiaSign & Date Page 1 of 2

Candidate Should have experience in Spring manufacturing. To review the QMS process in the shop floor for the implementation and effectiveness ; To move the rejections on a daily basis into scrap area ; To Analysis of Data. & Action to Achieve KPI (customer / in-house PPM) ; To monitor and review Part identification and Traceability records ; To follow and review process as per Work standard ; To monitor and review the rework with actions ; To update the Error proofing / Product safety working conditions to achieve product quality ; To update the Error proofing / Product safety working conditions to achieve product quality ;

As a member of the ACG Capsules team based in Shirwal, your primary responsibilities will include: - Checking the allocated post production (ATS/Printing/camera) line(s) during each shift according to the CTQ (Critical to Quality) / CTP (Critical to Productivity) checklist. - Following the plan outlined in the color change note to minimize change over time at each sub-section. - Adhering to instructions from the shift lead to ensure timely change over by making sure roller(s)/ink are available. - Performing In-Process Quality Checks (IPQC) after every roller cleaning and checking camera rejections hourly to achieve zero defects. - Operating cameras according to the Standard Operating Procedures (SOP) to attain productivity and quality goals. - Collaborating with contract associates to ensure SOP compliance at ATS/Camera/packing/Sealing and tumbling stages. - Implementing preventive maintenance plans for the line(s) to minimize downtime and achieve operational efficiency. - Conducting troubleshooting activities for the entire line(s) to enhance productivity, seeking maintenance team support when necessary. - Monitoring and controlling post-production losses in printing and camera operations to meet the Targeted AFOE@Despatch. - Adhering to cGMP and GDP guidelines for the allocated line(s) to ensure regulatory compliance throughout the shift. - Following instructions from the shift lead/team lead to implement Corrective and Preventive Actions (CAPA) for any customer complaints. Key Result Areas for this role include: - Productivity of the line - Print loss, print reject, and camera loss - Safety - SOP Adherence You will interface with: - ITI - Freshers Your success in this role will depend on your competencies and ability to effectively execute the outlined responsibilities.,

The Quality Inspector will have the overall responsibility for various aspects of daily IPQC, IQC, FQC, and PDI for Pre & Post Lam processes at Dudu - Jaipur. The ideal candidate should have an ITI/ Diploma/ B.Tech qualification along with 2 to 6 years of relevant experience. If you possess the ability and qualifications to not only work in but also create an ever-growing environment, then come join GREW. Growth is the core evidence of life, fueled by our infinite imaginations. We are constantly seeking talented individuals who resonate with this vision. To apply for the position of Quality Inspector, kindly send your resumes to careers@grew.one.,

As a member of ACG Capsules in Shirwal, your primary responsibilities include checking the allocated post production line(s) such as ATS/Printing/camera in each shift according to the CTQ (critical to Quality) / CTP (Critical to Productivity) checklist. You will need to adhere to the plan outlined in the color change note, minimizing change over time at each sub-section. Following instructions from the shift lead is crucial for timely changeover, ensuring the availability of necessary equipment like roller(s) and ink. Furthermore, it is essential to execute In-Process Quality Control (IPQC) after each roller cleaning, checking camera rejections hourly to achieve zero defects. Operating the camera according to Standard Operating Procedures (SOP) is vital to maintain productivity and quality standards. Collaboration with contract associates is necessary to ensure SOP compliance at ATS, Camera, Packing, Sealing, and Tumbling sections. You will be responsible for implementing preventive maintenance plans for the line(s) to minimize downtime and conducting troubleshooting activities to enhance productivity. Reporting and controlling post-production losses of printing and camera operations are crucial for achieving the Targeted AFOE@Despatch. Adhering to cGMP and GDP for the allocated line(s) is essential to comply with regulatory standards during the shift. Additionally, following instructions from the shift lead or team lead to implement Corrective and Preventive Actions (CAPA) for any customer complaints is part of your duties. Key Result Areas for this role include ensuring productivity of the line, managing print loss, print reject, and camera loss, prioritizing safety measures, and adhering to Standard Operating Procedures (SOP). In this role, you will interface with ITI candidates, as well as freshers. The competencies required for this position include [Competencies to be filled based on the job description provided].,

Position Summary: The Head of Quality will be responsible for overseeing all quality assurance, quality control, and supplier quality management processes for Lenskarts manufacturing facility in Bhiwadi. This role is critical to ensuring the delivery of high-quality products that meet Lenskart's standards and customer expectations. The incumbent will drive continuous improvement initiatives, manage quality metrics, and implement effective quality control systems, particularly in areas such as Critical to Quality (CTQ) processes and Supplier Quality Assurance (SQA). Key Responsibilities: 1. Quality Strategy and Leadership: Develop and implement a comprehensive quality management strategy aligned with Lenskart's overall manufacturing and business objectives. Lead, mentor, and manage the quality team to foster a culture of continuous improvement and customer focus. Collaborate with cross-functional teams (production, engineering, supply chain) to ensure quality considerations are integrated into all aspects of the production process. 2. Quality Control & Assurance: Design and enforce quality control standards to ensure all products meet or exceed established quality metrics and regulatory compliance. Oversee the deployment of quality management systems (QMS) and ensure adherence to ISO standards or equivalent certifications. Utilize advanced quality tools like FMEA, SPC, MSA, and Six Sigma techniques to monitor and improve production quality and reduce defects. 3. Critical to Quality (CTQ) Management: Define, implement, and continuously monitor CTQ parameters for various processes and products to guarantee consistent quality. Ensure CTQ data is effectively used to detect potential quality issues early in the production process. Collaborate with design, engineering, and production teams to align on CTQ requirements and identify improvement areas. 4. Supplier Quality Assurance (SQA): Lead the SQA process, working closely with suppliers to improve incoming material quality and ensure alignment with Lenskarts standards. Conduct regular supplier audits and implement corrective actions where necessary. Develop and manage robust supplier evaluation and qualification processes, including performance metrics and improvement plans. 5. Quality Improvement and Problem-Solving: Lead problem-solving activities using techniques like Root Cause Analysis (RCA), 8D, and Lean methodologies to address recurring quality issues. Identify and implement cost-effective quality improvements that enhance product reliability and manufacturing efficiency. Champion the use of statistical analysis and Six Sigma tools to reduce process variation and drive continuous improvement. 6. Quality Compliance and Reporting: Ensure compliance with local, national, and international regulatory standards relevant to the optical and eyewear industry. Develop and maintain dashboards and KPIs to monitor quality performance and generate regular reports for senior management. Implement effective quality data management and reporting systems to ensure accurate tracking of all quality metrics and trends. 7. Training and Development: Develop training programs for the quality team and production staff to promote best practices in quality management. Ensure team proficiency in quality methodologies, statistical tools, and quality-related technologies. Facilitate workshops and training sessions on CTQ, SQA, and other quality standards for continuous capability building. Qualifications and Requirements: Education: Bachelors degree in Engineering (Mechanical, Industrial, or related field); Master’s degree is preferred. Certification in quality management (such as Six Sigma Black Belt, ISO Lead Auditor, etc.) is strongly preferred. Experience: 13-18 years of experience in Quality Management in a manufacturing setup, ideally with exposure to high-volume consumer products. Proven experience in CTQ, SQA, Lean Manufacturing, and Six Sigma methodologies. Solid experience with quality tools and techniques, including FMEA, SPC, MSA, RCA, and CAPA.

Dear Candidiates, We are hiring for an quality engineers, candidate must have experience in IQC, IPQC or OQC, Job Location : Ecotech Ext 1, Greater Noida Education Required : Diploma/B.tech in Electrical