37 Iqc Jobs

As a member of the Group Company team, your primary responsibilities will include managing and coordinating various tasks and projects within the organization. You will be responsible for ensuring the smooth operation of day-to-day activities, as well as contributing to the overall success of the company. Your role will require you to work closely with team members from different departments to achieve common goals and objectives. Your key result areas will involve monitoring and analyzing key performance indicators to track progress and identify areas for improvement. You will be expected to generate reports and present findings to senior management, providing valuable insights that will help drive strategic decision-making. Additionally, you will play a key role in implementing and maintaining operational processes to enhance efficiency and productivity. In this position, you will have the opportunity to interact with various stakeholders, both internal and external, to build and maintain positive relationships. You will collaborate with cross-functional teams, vendors, and clients to ensure alignment on project goals and deliverables. Your ability to communicate effectively and foster strong partnerships will be crucial to your success in this role. To excel in this position, you should demonstrate a range of competencies, including strong analytical skills, attention to detail, and the ability to multitask effectively. You should be a proactive problem-solver with a results-driven mindset, capable of working independently and as part of a team. Adaptability, resilience, and a customer-focused approach are also essential attributes for success in this dynamic and fast-paced environment.,

As a Material Planner, your primary responsibility will be to manage monthly MRP activities, including Min Max and Main MRP. You will be required to update ERP masters such as Party master as needed. Additionally, you will handle PR GD updation, Min Max PR, and Main MRP PR. Your role will involve tasks such as Import Parts Ordering, PCB Ordering, and updating the status of orders by communicating with sales engineers, customers, and production teams. You will also be responsible for PPCB Assembly Planning, Semi-finished Planning, and following up on missing raw materials with the Purchase department. Furthermore, you will oversee the closure of missing items with the stores, coordinate with IQC for urgent parts/PPCB/SFG QC, and manage SO Based MRP. Collaboration with vendors to ensure timely delivery of SFG and PPCB will also be a part of your duties. Overall, your role as a Material Planner will require effective communication, meticulous planning, and coordination with various internal departments and external stakeholders to ensure smooth and efficient material management processes.,

Role & responsibilities Lead and manage Incoming (IQC), In-Process (PQC), and Final Quality Control (FQC) processes. Interface with customers, vendors, and cross-functional teams for quality audits, inspections, and approvals. Champion Root Cause Analysis (YY analysis) and drive implementation of effective Corrective and Preventive Actions (CAPA). Ensure compliance to Defense and Aerospace quality standards in design, development, and manufacturing stages. Maintain and continuously improve QMS documentation including SOPs, work instructions, inspection reports, and quality plans. Lead internal and external quality audits, certifications, and statutory compliance. Facilitate cross-departmental coordination for issue resolution and process improvements. Present quality metrics, dashboards, and improvement initiatives to the Managing Director and Senior leadership. Contribute to product and process improvement initiatives, particularly in projects related to Telescopic Masts, Positioners, Tripods, and Power Electronics. Key Skills and Competencies: - Strong understanding of Ok-Ok analysis, and critical inspection points. Solid grasp of ISO/AS9100, ISO 9001 , and other relevant Defense/Aerospace Quality Systems. Proficiency in technical documentation, SOP creation , and QMS tools. Excellent communication, presentation , and stakeholder management skills. Hands-on experience with machining, sheet metal, electronic assembly, and system integration is preferred. Familiarity with defense and Aerospace manufacturing protocols, audit processes , and engineering documentation standards . Desired Candidate Profile: 15+ years of progressive experience in Quality Assurance & Control in Aerospace or Defense manufacturing . Demonstrated capability in leading quality functions , including audits, documentation, and compliance. Experience working directly with customers, OEMs, and defense procurement teams . Should be self-driven, detail-oriented, and possess strong problem-solving and analytical skills.

Good knowledge about sampling plan and IQC control plan,Should know the Incoming quality control lab process in any EMS industry,Should know prepare the SOP & SIP and LRR,Daily basic process schedule & Tracking.Skill in yield and production process in EMS. Incomming Quality Control, Supplier Quality Engineering,,Online Relaiability Test,Process Quality Control, 1. Responsible for Leading the Quality function and day to day In-process Quality verification with consistent result both in terms of Quality and Quantity to meet daily plant output/customer requirements. 2. Performing in-process quality inspection for accuracy, specification parameters and workmanship. Develop and implement best quality processes in production 3. Tabulate and document data relating to products, processes, materials, its qualities, and reliabilities 4. Train staff, technicians, and professionals on the aspects of quality control activities. 5. Troubleshoot and resolve problems relating to quality using quality tools (DMAIC, 8D, 4Q, PDCA etc.) Capture and analysis of COPQ in order to achieve savings. 6. Conducting regular Inspections and Audits to assess product quality and compliance with established standards 7. Collaborating with production teams to Identify areas for improvement and develop solutions to address quality Issues.

IQC (Incoming Quality Control) SQA (Supplier Quality Assurance) IPQC ( In Process Quality Control) Strong SMT Components Knowledge Must

IQC (Incoming Quality Control) SQA (Supplier Quality Assurance) IPQC ( In Process Quality Control) Strong SMT Components Knowledge Must

Role & responsibilities The Central Laboratory Manager will lead and manage operations of the Central Lab at Ankura Hospital, ensuring standardized, efficient, and high-quality diagnostic services across all Ankura Hospital branches. This role involves managing centralized testing, maintaining NABL/NABH compliance, streamlining inter-branch sample logistics, and ensuring consistency in lab quality, TAT, and reporting standards across the network. Central Lab Oversight: Manage the core operations of Ankuras Central Lab, overseeing all major diagnostic modalities (Biochemistry, Microbiology, Hematology, Pathology, Immunology, etc.). Ensure timely processing and reporting of samples received from all Ankura locations. Maintain a centralized reporting dashboard for lab performance across branches. Multi-Location Coordination: Work closely with Lab Technologists, Quality Leads, and Unit Heads across branches to ensure sample collection, transportation, and reporting are aligned with SLAs. Monitor and audit branch labs to ensure sample integrity, documentation accuracy, and protocol adherence before dispatch to the Central Lab. Act as the single point of contact for all lab-related escalations across units. Quality & Accreditation Management: Ensure that the Central Lab complies with NABL standards and maintains readiness for surveillance audits. Harmonize SOPs across branches for pre-analytical, analytical, and post-analytical processes. Implement internal quality control (IQC) and participate in EQAS programs for inter-lab accuracy checks. Team Leadership & Development: Lead a team of senior technologists, quality officers, phlebotomy coordinators, and support staff at the Central Lab. Conduct regular training and assessments to upgrade skills of lab teams across units. Drive a culture of process discipline, accountability, and continuous improvement. Technology & LIS Oversight: Oversee the implementation and usage of LIS(Laboratory Information System) across branches and central lab. Collaborate with IT to ensure seamless data flow, auto-validation, and centralized report access. Work with OEMs and vendors for analyzer integration, calibration, and preventive maintenance. Sample Logistics & Inventory: Develop and manage an efficient sample transportation system from branches to the Central Lab, with TAT adherence. Ensure optimal inventory of reagents, consumables, and supplies at the central lab and monitor reorder levels across units. Streamline vendor relationships and procurement coordination with central supply chain team. Performance Monitoring & Reporting: Establish KPIs for lab operations across all unitsTAT, error rates, EQAS scores, equipment downtime, etc. Monitor and present CPRT (Cost Per Reportable Test) and Lab Cost Analysis Publish monthly dashboards and operational reports to management with analysis and improvement actions. Ensure patient feedback related to lab services is reviewed and addressed promptly. Job Specifications Educational Qualification M.Sc. in Medical Lab Technology (MLT) / Microbiology / Biochemistry / Life Sciences (MBA in Healthcare Management preferred) Experience: Minimum 10 years in hospital lab services, with at least 3-5 years managing centralized or multi-site operations in a NABL-accredited environment. Certifications: NABL Internal Auditor Certification preferred but not mandatory Work Location: Attapur Must be flexible to travel.

Role & responsibilities The Central Laboratory Manager will lead and manage operations of the Central Lab at Ankura Hospital, ensuring standardized, efficient, and high-quality diagnostic services across all Ankura Hospital branches. This role involves managing centralized testing, maintaining NABL/NABH compliance, streamlining inter-branch sample logistics, and ensuring consistency in lab quality, TAT, and reporting standards across the network. Central Lab Oversight: Manage the core operations of Ankuras Central Lab, overseeing all major diagnostic modalities (Biochemistry, Microbiology, Hematology, Pathology, Immunology, etc.). Ensure timely processing and reporting of samples received from all Ankura locations. Maintain a centralized reporting dashboard for lab performance across branches. Multi-Location Coordination: Work closely with Lab Technologists, Quality Leads, and Unit Heads across branches to ensure sample collection, transportation, and reporting are aligned with SLAs. Monitor and audit branch labs to ensure sample integrity, documentation accuracy, and protocol adherence before dispatch to the Central Lab. Act as the single point of contact for all lab-related escalations across units. Quality & Accreditation Management: Ensure that the Central Lab complies with NABL standards and maintains readiness for surveillance audits. Harmonize SOPs across branches for pre-analytical, analytical, and post-analytical processes. Implement internal quality control (IQC) and participate in EQAS programs for inter-lab accuracy checks. Team Leadership & Development: Lead a team of senior technologists, quality officers, phlebotomy coordinators, and support staff at the Central Lab. Conduct regular training and assessments to upgrade skills of lab teams across units. Drive a culture of process discipline, accountability, and continuous improvement. Technology & LIS Oversight: Oversee the implementation and usage of LIS(Laboratory Information System) across branches and central lab. Collaborate with IT to ensure seamless data flow, auto-validation, and centralized report access. Work with OEMs and vendors for analyzer integration, calibration, and preventive maintenance. Sample Logistics & Inventory: Develop and manage an efficient sample transportation system from branches to the Central Lab, with TAT adherence. Ensure optimal inventory of reagents, consumables, and supplies at the central lab and monitor reorder levels across units. Streamline vendor relationships and procurement coordination with central supply chain team. Performance Monitoring & Reporting: Establish KPIs for lab operations across all unitsTAT, error rates, EQAS scores, equipment downtime, etc. Monitor and present CPRT (Cost Per Reportable Test) and Lab Cost Analysis Publish monthly dashboards and operational reports to management with analysis and improvement actions. Ensure patient feedback related to lab services is reviewed and addressed promptly. Job Specifications Educational Qualification M.Sc. in Medical Lab Technology (MLT) / Microbiology / Biochemistry / Life Sciences (MBA in Healthcare Management preferred) Experience: Minimum 10 years in hospital lab services, with at least 3-5 years managing centralized or multi-site operations in a NABL-accredited environment. Certifications: NABL Internal Auditor Certification preferred but not mandatory Work Location: Attapur Must be flexible to travel.

The IQC Inspector is responsible for inspecting and verifying incoming electronic components, PCBs, and raw materials to ensure they meet the companys quality standards and customer specifications in the EMS industry. Key Responsibilities: Inspect incoming electronic components, PCBs, mechanical parts, and other materials based on specifications, drawings, and IPC standards. Diploma mEchanical with 2 years of experience in Quality of EMS industry can apply Send resumes to malavika.pradeep@nestgroup.net

The IQC Inspector is responsible for inspecting and verifying incoming electronic components, PCBs, and raw materials to ensure they meet the companys quality standards and customer specifications in the EMS industry. Key Responsibilities: Inspect incoming electronic components, PCBs, mechanical parts, and other materials based on specifications, drawings, and IPC standards. Diploma mEchanical with 2 years of experience in Quality of EMS industry can apply Send resumes to malavika.pradeep@nestgroup.net

As a Production and Service Engineer at our company, you will play a crucial role in the assembly, fitting, testing, calibration, and servicing of our products. Your primary responsibility will be to ensure that all tasks are completed according to the Standard Operating Procedures (SOP) to deliver high-quality products to our valued G-Tek customers within the expected standards and timelines. To qualify for this role, you should have a Diploma in Electronic and Communication Engineering. Your key deliverables will include performing assembly, testing, fitting, machine operation, material handling, and maintaining accurate data records. Additionally, you will be responsible for conducting Incoming Quality Check (IQC) and Outgoing Quality Check (OQC), prioritizing personal safety and compliance, providing customer support both online and offline, and ensuring a clean and organized work environment. Your daily tasks will involve reviewing work orders, issuing materials from the store, assembling products based on product codes and SOPs, conducting final tests on products, and recording necessary data. You will also be required to inspect finished products and components for quality assurance, interact with customers for repairs and service, and maintain cleanliness and organization in your workstation and production area. Furthermore, your performance will be measured based on key metrics such as First Pass Yield (FPY) data exceeding 99%, on-time production exceeding 95%, inside warranty turnaround time of less than 3 days, and 100% compliance with on-time data filling and entry. This is a full-time position with benefits including health insurance, leave encashment, and Provident Fund. The work schedule will be during day shifts, and candidates with a Diploma qualification and at least 1 year of work experience are preferred. If you have availability for day shifts and can work in person at our designated location, we encourage you to apply for this exciting opportunity to be a valuable part of our production and service team.,

•To Handle the incoming, Inprocess, Final Inspection Quality. •Handling Customer Complaint. •Knowledge of 5 Core Tools, IQC Tools, IPC, IP, NPD etc & 8D. •Have work Experience with same types of Industries. Knowledge of machining

Role & responsibilities Experience on EMS based Industry must Handling of supplier and Customer through mail conversation with good communication Skill. • Knowledge on IPC 600, IPC 610 & J STD • Hands on SCAR/RCCA/8D against Incoming & Online material Issues • Involved in ECN/ECO process • Experience in Sampling Plan, AQL, SIP/SOP, Agile, SAP & BOM • Preparing & Presenting report for customers • Knowledge on Rejection Analysis, 7 OC tools, PPAP & Quality Core Tools Preferred Mobile Manufacturing Industry experience Preferred candidate profile EXCEL, Power Point Excellent verbal & mail Communication Team Player Education Qualification Bachelor of Engineering (EEE/ECE/EI)

Inprocess Quality control engineer required at kundli sonipat Qualification- Diploma/ b.tech electronics Exp- min 2 yrs Salary- upto 25k- 30k Skills- Power bank, charger, earphone timing- 9 to 6

Plant Quality – MQC Plant Quality - RQC & Customer QA Quality Assurance Customer Quality Incoming Quality Proficiency in quality standards (IATF 16949: 2016, ISO 9001:2015, 6 Core Tools etc.) Internal audit, Process and Product audit

Posted On 03rd Apr, 2025 : Role Overview: The Quality Head will be responsible for defining, implementing, and maintaining world-class quality assurance strategies across manufacturing operations, supplier quality, regulatory compliance, and injection molding processes. The role requires strong leadership, analytical thinking, and expertise in industry best practices to promote a strict quality control culture within the organization. Key Responsibilities: Quality Strategy & System Implementation Develop and implement Quality Assurance (QA) and Quality Control (QC) systems aligned with ISO 9001, ISO 14001, ISO 45001 (Occupational Health & Safety), and ESD S20:21 (Electrostatic Discharge Protection). Define and drive KPIs for quality performance, including First Pass Yield (FPY), Defect Per Million Opportunities (DPMO), and Cost of Poor Quality (COPQ). Establish and ensure strict adherence to Standard Operating Procedures (SOPs) for inspection, testing, and validation at every stage of production. Promote a strict quality control culture across all teams, ensuring that every employee understands the importance of quality in manufacturing. Manufacturing of LED TVs, Injection Moulding & Supplier Quality Management Oversee incoming (IQC), in-process (PQC), and final product quality (OQC)to minimize defects and rework. Implement Electrostatic Discharge (ESD) Protection (ESD S20:21) measures to ensure the safety and reliability of electronic components. Work closely with suppliers to improve the quality of raw materials, plastic components, and electronic parts. Conduct supplier audits and enforce compliance with RoHS, REACH, and BIS standards. Manage and optimize injection molding quality control, including: Material selection and testing (resins, polymers). Process parameter optimization to minimize defects such as warping, sink marks, and short shots. Implementation of real-time monitoring and defect detection technologies. Ensuring compliance with industry best practices for plastic components used in electronic products. Compliance & Certifications Ensure compliance with ISO 9001, ISO 14001, ISO 45001, BIS, RoHS, CE, FCC, and other global regulatory requirements. Lead internal and external audits for regulatory approvals and maintain all necessary certifications. Develop and maintain safety and environmental management systems aligned with international best practices. Customer Quality & Market Feedback Analyze customer complaints, warranty claims, and field failures to identify trends and implement Corrective and Preventive Actions (CAPA). Drive continuous improvement initiatives to reduce product returns, warranty costs, and customer dissatisfaction. Collaborate with the after-sales service team to track product performance and reliability in the field. Continuous Improvement & Innovation Implement Lean, Six Sigma, and Kaizen methodologies to drive continuous quality improvement. Introduce automation and AI-based quality inspection techniques to enhance production efficiency. Develop and conduct regular training sessions to ensure all employees, from factory workers to management, understand and adhere to quality standards. Promote a zero-defect mindset within the organization, ensuring proactive rather than reactive quality management. Key Qualifications & Experience: EducationBachelors/Masters degree in Engineering (Electronics, Mechanical, Manufacturing, or Polymer Science). Experience12+ years in Quality Management, preferably in electronics, home appliances, or automotive manufacturing. Expertise in ISO 9001, ISO 14001, ISO 45001, ESD S20:21, Six Sigma (Green/Black Belt preferred), and SPC (Statistical Process Control). Experience with BIS, RoHS, CE, FCC, and other regulatory standards. Hands-on experience in injection molding quality control, defect analysis, and process optimization. Knowledge of AI-based quality inspection, ERP & Quality Management Software (SAP, MES, etc.) is a plus. Key Skills Required: Strong analytical and problem-solving skills (Root Cause Analysis, 8D, FMEA) Leadership and team-building experience in a factory setup Knowledge of global quality management systems Injection moulding quality control & process optimization Experience with ERP & Quality Management Software (SAP, MES, etc.) Ability to collaborate with R&D, Manufacturing, and Supply Chain teams Why Join Be a part of a fast-growing company with innovation-driven leadership and legacy. Opportunity to implement cutting-edge quality processes in electronics and injection molding. Work with a dynamic and high-impact team in a competitive industry. Key Skills : Company Profile Company is ---s most trusted and leading ODM/OEM brand with a complete Made in --- design, development, and manufacturing process. Established in 1984, is one of ---s leading ODM/OEM manufacturers with four decades of industry expertise. As the official ODM for webOS TV in --- and the only TV ODM with a Dolby License, the company focuses on backward integration to optimize costs and enhance production. With a current manufacturing capacity of 1.4 million units per annum, expanding to 3.2 million with a new facility, Company is set to become a major player in ---s electronics manufacturing sector. Its expertise in hardware and software enables it to deliver high-performance products, reinforcing ---s global technology manufacturing capabilities.

Greetings from Thyrocare! Hiring *Quality Executive* for *Thyrocare Technologies Limited.* Job Locations/RPL : D No: 29-5-1, Shyam Enclave, opp. glaxo, Cherukupalli vari St, Governor Peta, Vijayawada, Andhra Pradesh 520002. Qualification - BMLT,DMLT,MLT Certification ISO15189 MUST Job Description : 1. >2 years experience in Quality assurance 2. Adequate exposure of Internal audits 3. Adequate exposure in external audits NABL, CAP etc 4. Will be on travelling profile 5. Preparing the assigned labs for NABL audits , conducting internal audits 6. Monitoring the assigned labs for Quality assurance, IQC , EQAS, IQC outliers, CV% etc 7. Preparing SOPs , QSPs If any one is interested kindly share your resume Email ID : mitu.jena@thyrocare.com Or whatsaap : +91 9321414235 Regards, Mr. Mitu Jena Contact No: 9321414235 Sr. HR | Talent Acquisition Thyrocare Technologies Ltd.

1) Familiar with the product processes 2) Quality Check For Mobile, Main Board & Display 3) Familiar in mobile & electronics market 4) Having Experience In Purley Service Center 5) The individual receives the faulty mobile phone, Mother board

Key Responsibilities: Lead and manage the plants quality team while fostering a culture of accountability and continuous improvement. Oversee quality testing and inspection activities across the factory and assembly lines. Ensure full compliance with ISO audits and maintain relevant certifications. Liaise with clients to meet audit and pre-delivery inspection requirements. Proactively identify and address quality issues in a timely manner. Continuously enhance quality systems, processes, and overall performance. Requirements: Degree or diploma in engineering (preferably mechanical, electrical, or industrial). Minimum 5 years of managerial experience in manufacturing quality. Strong communication skills in English and the local language. Excellent leadership and team management capabilities. Candidates from the electronics or manufacturing industries will be preferred.

Role & responsibilities Conduct inspection and testing of incoming raw materials, reagents, and components used in IVD product manufacturing. Review CoA, CoC, MSDS, and other supplier documents and ensure compliance with specifications. • Maintain and update incoming inspection records, logs, and release documents. Coordinate with vendors for material discrepancies, rejections, and corrective actions. Ensure that all materials are tested as per SOPs, QMS guidelines, and regulatory standards. Participate in vendor audits and provide inputs for supplier qualification. Collaborate with cross-functional teams including procurement, production, and R&D for material-related issues. Support in non-conformance investigation and initiate CAPA for recurring issues. Ensure calibration and maintenance of IQC instruments and equipment. Adhere to ISO 13485:2016, Good Documentation Practices (GDP), and applicable regulatory requirements. Regards, Muskan Vats muskan.v@head2hire.com

Role & responsibilities : 1.English Communication skills, 2.Good local launguage Communication Skills 3.Good Knowledge in Excel & PPT IQC Job Description: 1.Should know the Incoming quality control lab process in any EMS industry 2.Good knowledge about sampling plan and IQC control plan 3.Should know about inventory management and ageing control. 4.Have knowledge about conduct MRB meeting for rejection 5.Should know prepare the SOP & SIP and LRR. 6.Familiar with smartphones and process 7.should know about 5s/ESD/7QC tools knowledge 8.Should know the yield and production basic knowledge 9.Need manpower handling near 30x operators 10.Need strong knowledge on supplier quality process in EMS industry 11.Familiar to handle the suppliers domestic and international. 12.Strong knowledge about the 4m analysis and review the FACA 13.should know about 5s/ESD/7QC tools knowledge 14.Skill in yield and production process in EMS 15.Strong knowledge on vendor escalation and get corrective action PQC Job Description: • Responsible for Leading the Quality function and day to day In-process Quality verification with consistent result both in terms of Quality and Quantity to meet daily plant output/customer requirements. • Performing in-process quality inspection for accuracy, specification parameters and workmanship. Develop and implement best quality processes in production • Tabulate and document data relating to products, processes, materials, its qualities, and reliabilities. • Train staff, technicians, and professionals on the aspects of quality control activities. • Troubleshoot and resolve problems relating to quality using quality tools ( analysis of COPQ in order to achieve savings.DMAIC, 8D, 4Q, PDCA etc.) Capture and PDCAP-YY7 • Conducting regular Inspections and Audits to assess product quality and compliance with established standards. • Collaborating with production teams to Identify areas for improvement and develop solutions to address quality Issues. • Ensuring that all quality-related processes comply with local and international regulations and standards. • Providing training and support to production teams to improve their quality control skills and knowledge. • Reviewing customer feedback and using this information to identify areas for improvement. • Support during Customer Intections, QA drafting and approvals etc. Implementing Poka-Yoke wherever possible to prevent quality errors and improve safety level. • Support and lead continuous improvement programs, problem solving and process improvement activities. • Adhere to QMS, other company policies and procedures & Quality Documentation Control. • Strong Technical know-how about the Process flow. KAIZEN & ISO-9001 and 14001,45001 Documentation. • Strong Knowledge about the Corrective Action Plan (8D), Continual Process Improvement. • Shows moral courage, openness and honesty in all dealings. Good communication and interpersonal skill.

Preparation & updation of plans Inspection of plating, moulding,stamping child part as per quality plan Inspection of winding wire & Contacts, Inspection of resistor Diode Clearing & Monitoring GRN closing status MSA for instruments used in IQ Dept Required Candidate profile Preparation of Layout inspection of child part as per plan Potential supplier capability assessment SST plan Raw material testing plan & as per plan sending monthly samples for testing

Incoming Quality Control Executive (Female Candidate) - Industry: Plastic and Rubber Auto Components Manufacturing - Working Hours: 9:00 AM to 7:30 PM, Monday to Saturday - Key Responsibilities: - Inspect incoming raw materials and components - Conduct quality checks and identify defects - Collaborate with suppliers and maintain records - Implement quality control procedures - Requirements: - Degree in a relevant field - Experience in quality control (preferably in plastic and rubber industry) - Strong attention to detail and analytical skills Contact : +91 9211563028

Coordinating the daily operation and management of the QC team (OQC/, rationally arranging manpower supplements according to actual production schedules, and improving work efficiency. Required Candidate profile Engineering quality tools, Problem solving tools, 8D, 6Sigma, SPC and other quality tools. Core tools knowledge ERP/ SAP/ Oracle hands on experience Master the skills , Minitab, email etc.

We are looking for IQC Engineer at Nipro India Corporation Pvt Ltd. Qualification: DME/BE/M.Sc Chemistry/B.Pharmacy Experience : Minimum 3-5 Years Roles & Responsibilities: 1. Responsible for in process quality activities. 2. Control and solve daily quality problems in daily routine IQC activity. 3. CAPA for prevention of recurrence of complaints non confirmities and in - process non confirmities. 4. Follow up of CAPA 5. Accountable for the rework and rejection analysis 6. Control to follow up the SOP's and cGMP regulations in the working areas. 7. Find out or implement the new method or the way to improve quality of product. 8. Support to concern department for process control and set meeting to resolve the issue. 9. Training to subordinates about in process quality control 10. Prepare the report for quality meeting. 11. Preparation, Review and Updating of limit sample. 12. Support to Engineering and QAD department for calibration of all instruments in the section. 13. Establish, Review and Revise documents and quality record in section to update and follow the ISO. 14. Represent superior to join the meeting or co-ordinate inside and outside section in case he / she absent. 15. Responsible & completion of additional activity and task given by the section Head. 16. Responsible for reviewing of the artwork as per regulatory requirements. 17. Label printing and controlling 18. Rejection trend analysis. 19. Complaint Analysis. 20. Machine wise observation to contract defect. 21. Improvement on machine related to quality of production. 22. Monthly report at quality data objective 23. In process quality testing as well as controlling. 24. Label Printing and controlling 25. Monthly training of SOP to department employees. 26. Problem analysis and corrective action taken. 27. Material testing & Release in SOP system. 28. Manpower control. 29. Continuous improvement 5S & Kaizen 30. Responsible for reviewing and submitting of product DHR to quality department. Interested candidates kindly share your resume on shrawani.kadam@niproindia.com with mentioned subject "IQC Engineer - Your Name".