9170 Qc Jobs - Page 4

Qualification and Experience M.sc Biotechnology Experience in using a microscope is preferred. Other lab experience preferred but not must Job Description: On-farm/ Clinic work Routine QC and maintenance of lab equipment. Proper handling and storage of media Preparatory work for embryo/oocyte collection Assist veterinarians in embryo/oocyte. collection Search, evaluate, and grade oocytes and embryos Processing of bull semen for fertilization Fertilization of oocytes Culture of zygotes. Evaluation and grading of day 6 and day 7 embryos Loading and shipping of fresh embryos in shipping incubators Slow freezing or vitrification of embryos. Unloading fresh embryos from the shipping tubes and loading the ET guns Thawing frozen embryos and loading the ET guns for the veterinarians to do the transfers. Keeping an inventory of frozen semen doses (FSDs) and frozen embryos. Keeping an inventory of lab supplies, media, and consumables Order materials as per the requirement

We're Hiring – NDT Level II Quality Inspector (CS & SS Piping) 📍 Location: Hazira, Surat (Adani Port Project) 📅 Immediate Requirement Ambica Enterprise is looking for an experienced and certified NDT Level II Quality Inspector for our ongoing piping project involving 16" Carbon Steel and Stainless Steel line fabrication and erection . Role & Responsibilities: Conduct NDT (RT, UT, PT, MT) inspections as per project standards Review weld maps, WPS, PQR, and ITP Ensure compliance with client (Adani) quality requirements Coordinate with third-party inspection agencies and client QC teams Maintain accurate records and reporting for weld joints & test results Candidate Profile: ASNT/ISNT Level II certified in RT, UT, PT, MT Minimum 3–5 years’ experience in CS & SS piping (preferably 16” and above) Experience in port, oil & gas, or industrial infrastructure projects Knowledge of relevant codes (ASME, API, etc.) Ready to join at Hazira site immediately If you're passionate about quality and ready to work on a challenging and prestigious site, we’d love to hear from you. 📩 Apply now or share your CV at chirag@ambicaenterprise.co 📞 Contact: 95863 69791 / 99042 34020 #Hiring #NDTLevel2 #QualityInspector #HaziraJobs #AdaniPort #PipingJobs #CSandSS #AmbicaEnterprise #WeldingInspection #QAQCJobs

Position: QC Engineer No. of Positions: 3 Experience Required: 0-2 Years Salary Range: ₹15,000 per month, 3 Months Probation Reporting To: Production Supervisor Educational Qualifications: BE Mechanical/Production Primary Responsibilities Shift Report Verification Check and verify night shift QC reports for accuracy and completeness at the beginning of your shift. Shift Report Book Maintenance Update the Shift Report Book with verified details from the previous shift and maintain logs throughout your own shift. In-Process Quality Checks Conduct in-process inspections at defined stages of production and document findings in the In-Process QC Report. Deviation & Rejection Handling Immediately highlight any deviations or rejections to the Production In-Charge for necessary corrective action. Non-Conformance Reporting Record all non-conformances (NCs) and submit detailed NC reports to the Production In-Charge. Incoming Material Inspection Perform inspection of incoming raw materials or components as and when required, and prepare corresponding reports. Part Traceability Verification Ensure that serial numbers of all parts are properly matched and recorded against inspection reports. Shift-End QC Reporting Submit all compiled QC reports to the QC In-Charge at the end of each shift. Documentation & Reporting Responsibilities In-Process Inspection Report Maintain a comprehensive record of ongoing inspections and observations. Incoming Inspection Report Document material inspection results with batch and supplier references. NC Register Maintain a logbook/register of all non-conformances for internal review and analysis. Job Type: Full-time Pay: From ₹15,000.00 per month Ability to commute/relocate: Anand, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Work Location: In person

Title: Sr. Executive Custom Field 2: 2738 Location: Bavla, Gujarat, IN Country/Region: IN State: Guja City: Bavla Company: Dishman Carbogen Amcis Limited Business Unit: General Travel Description: Planning of spares and consumables for better inventory and budgetary control as per approved norms. Cost effective and quality vendor development for engineering materials and services. To check purchase requisitions and contractor service bills. To prepare and review User requisition Specification (URS). Co - ordinate with consultant and vendors for different activates of project. Procurement and erection & commissioning activities for projects. To review project related documents (Design basis, layouts, P&ID's, GA drawings and control philosophy etc.) and ensure its implementation accordingly. To execute and monitor project activities and ensure quality. To review and ensure timely compliance of maintenance services to plant operation in coordinate with cross functional team like QA, QC, Production, Warehouse, Safety, HR, Finance and IT. Proper utilization of available manpower & manufacturing facilities for smooth operation of engineering activities. To ensure the optimization usage of resources for reduction in waste. To review and ensure the compliance of safety regulation and guidelines. Preparing, controlling budgets for OPEX (material, consumables etc.) & handling CAPEX related to instrumentation and control. Preparation and review of Risk Assessment. Responsible for Green field and brownfield project concepts, plant designing, erection, commissioning & start-up of projects related to instrumentation. To ensure completion of preventive maintenance, calibration activities, validation activities and ensure timely compliance as per schedule. Checking of contractor's bills as per BOQ. Proper utilization of available manpower to expedite the maintenance and project activities. Execution and completion of maintenance and project work with respect to instrumentation. To ensure backup procedures are followed and backup of control system has taken by team member as per schedule. Preparation, review, implementation of SOP's of engineering department. To review and ensure the compliance of cGMP documentation and regulatory documentation and proper record of the same. To prepare, review and update lists, training documents, master list, calibration planner, validation documents & other CGMP documents. Generation & review of history cards, organogram, job responsibilities, qualification / validation documents, layouts, P&IDs, Calibration, PLC/DCS Validation, written procedure including amendments / addendum if any. To review & evaluate QMS activities (Like change controls, Deviations, Investigations, CAPA etc. Preparation and review of documents required for legal metrology, regulatory affairs etc & its compliance. Ensure online documentation related to all cGMP activities including data integrity. Preparation and execution of various planners / schedules Strict adherence to safety, health and environment. Harmonization of GMP practices among all manufacturing blocks within the facility. To fulfil the current needs of training with respect to GMP, GLP, Safety & Hygiene, job, application etc. To provide training to team members as per requirement and ensure all team members completed their training as per CGMP requirement. Adhere to all the company policies & manuals (business, safety and finance etc.) Any other assignments allocated by reporting function(s). Job Segment: Facilities, Compliance, Regulatory Affairs, Engineer, Instrumentation, Operations, Legal, Engineering

Position: Officer / Sr. Officer – Quality Control Grade: G12C / G12B No. of Position: 1 No. Job Location: Ahmednagar Qualification: M.Sc. (Chemistry) Experience: 5 to 9 yrs experience in API manufacturing plant Job Profile To investigate LAB Event, OOS/OOT results, Un-Planned deviation, Planned Deviation in all Section and timely submit for approval. To prepare and review the laboratory investigation report hypothesis study / evaluation study protocol and reports. To review of Analytical data like packing material, In-Process samples, Intermediate samples, Raw material and Finished Product samples, Stability samples etc. To review of instruments log books and other log books like IC Column, LCMS Column and WRS Log books etc. To ensure effective review of physical and electronic raw data and records generated in QC laboratory Review sample set and instrument methods, custom field related activity in Empower 3 software To review Audit trail of laboratory instrument which are connected with software like EMPOWER, LAB X, LAB Solution etc. To co-ordinate and conduct self inspection (internal audit) and its compliance To execute and review change control proposals in TRACK WISE. To monitor the compliance with the requirements of Good Manufacturing Practice and Good laboratory practice. To participate in management reviews of process performance, product quality and of the quality management system and advocating continual improvement. To ensure a timely and effective communication and escalation process exists to raise quality issues to appropriate levels of management. To conduct training program and ensure its effectiveness To Co-ordinate and manage with other department of the plant to build continuous quality in product and systems with technical support to get customer satisfaction. To co-ordinate with contract laboratory and full fill the requirements as per responsibilities section in technical / quality agreement and extend support as per requirements.

Company: Avanscure Lifesciences Pvt. Ltd. Industry: Pharmaceuticals / Life Sciences / Chemical Manufacturing Experience Required: 5+ Years About Avanscure: Avanscure Lifesciences Pvt. Ltd. is a leading manufacturer and global supplier of Active Pharmaceutical Ingredients (APIs), intermediates, and nutraceuticals. Operating in over 30 countries, we are recognized for our commitment to quality, innovation, regulatory compliance, and client success. As we scale aggressively across geographies, we seek results-driven professionals to lead our growth strategy in domestic and international B2B markets. Position Overview: We are looking for a high-performing Sales Manager to drive revenue growth, expand our customer base, and strengthen client relationships globally. This role demands strategic thinking, strong domain knowledge, and a proven ability to deliver results in competitive API and pharma markets. Key Responsibilities: Revenue Ownership: Take full ownership of monthly, quarterly, and annual sales targets and deliver consistent growth in assigned territories. Business Development: Identify and develop new B2B opportunities in APIs, intermediates, and nutraceutical segments across domestic and international markets. Client Relationship Management: Build and nurture long-term relationships with key decision-makers in pharmaceutical companies, CROs, CMOs, and distributors. Sales Operations & Execution: Generate and respond to RFQs, lead price negotiations, close high-value deals, and ensure timely execution through coordination with production, R&D, QA/QC, and logistics. Market Intelligence: Track competitor activity, pricing trends, and regulatory developments to inform strategic decisions and maintain a competitive edge. Team Leadership (if applicable): Guide, mentor, and drive a team of sales executives to meet collective performance goals. Reporting & Forecasting: Prepare sales forecasts, pipeline reports, and performance dashboards for leadership review. Industry Engagement: Represent Avanscure at international trade shows, exhibitions, and client meetings to build the brand and generate leads. Key Requirements: Bachelor's or Master’s degree in Pharmacy, Chemistry, Life Sciences. (MBA in Marketing/International Business is a plus) Minimum 5+ years of proven experience in B2B/API/chemical sales (preferably with exposure to international markets). Strong client network and industry connects in pharma and allied sectors. Excellent communication, negotiation, and stakeholder management skills. Proficient in CRM systems, Excel, PowerPoint, and sales reporting tools. Self-starter mindset with a strong sense of accountability and ownership. What We Offer: Attractive fixed + variable compensation package linked to performance. Exposure to leading global pharmaceutical clients and markets. Entrepreneurial work culture with high ownership and learning. Clear growth path and leadership opportunities in a fast-scaling company. How to Apply: Email your resume to sales@avanscure.com or contactgjs @avanscure.com with the subject: “Application for Sales Manager – [Your Name]”

Key Responsibility Areas: Collaborate with the Quality Manager to secure resources for optimal E2E Customer Quality Management, including systems and methods. Conduct field failure analysis of electrical components such as In-Vehicle Infotainment (IVI), Instrument Clusters (IC), Cockpit Domain Controllers (CDC), Sensors, PCBA, ECU, Harnesses, etc. Expertise in PCB testing and analysis, with in-depth knowledge of electronics manufacturing and testing in the automotive sector. Proficient in CAN Tool operations, log collection (including CAN logs, VST, and System logs), and data analysis. Strong understanding of displays, optics, display drivers, and Human-Machine Interface (HMI) systems. Analyze 0KM and warranty data, manage Warranty Signoffs, and authorize debit requests at the customer end. Maintain and review Customer Quality MIS and provide regular updates to the Quality Manager. Apply problem-solving techniques such as 8D, FTA, Fishbone Analysis, Why-Why Analysis, and 7QC tools. Manage a team of QREs across West and North regions. Develop data dashboards using Excel, SharePoint, and PowerPoint for effective data management. Contribute to plant-level management reviews with relevant data and insights. Initiate root cause analysis promptly, ensuring implementation of Corrective Actions (CA) and Preventive Actions (PA) for non-conformances and deviations. Identify and monitor opportunities for continuous improvement. Represent customer needs internally to meet QMS requirements, including quality goal setting, training, and CAPA processes. Ensure compliance with legal and regulatory requirements as per customer contracts. Oversee customer satisfaction metrics and maintain strong customer relationships. Visit customer sites for part performance reviews and handle customer complaints. Review and analyze non-conformance issues, both in-house and at the customer end. Identify and manage QA-related risks, both internally and externally. Ensure standardized work practices are in place and followed by QREs. Align audit processes with customer feedback and product standards. Collect and analyze quality assurance data to drive improvements. Coordinate with the QMS Representative on IATF16949:2016 compliance and market quality requirements. Initiate corrective actions for non-conforming products (DRR), customer complaints, and process instabilities. Authorize production/shipment halts if deviations affect fit, function, safety, or product compliance. Oversee FTR, PPAP, FTN, PTR activities, and related documentation. Job Specific Prerequisite: Qualification: Diploma or Graduate Engineer in Electronics, with mandatory experience in Quality Assurance in Auto Ancillary, ISO 9001/IATF16949, and VDA6.3 background. Must possess Voice of Customer and warranty system knowledge. Customer Exposure: Experience with Skoda Auto Volkswagen, Mahindra & Mahindra, Tata Motors, Hyundai, Maruti-Suzuki, Kia, HMSI , HMCL. Language Proficiency: Fluent in English, Hindi, Marathi, and Tamil Experience: 6-11 years in Quality. Preferred Companies: OEM E&E and Tier-1 Automotive Electronic Product Manufacturers. Notice Period: 2-3 months. Knowledge & Skills: Proficiency in problem-solving methodologies. Expertise in core quality tools like APQP, PPAP, FMEA, SPC, MSA, and 7 QC tools. Strong analytical and leadership capabilities. IATF 16949 Internal Auditor certification. Customer-focused with excellent communication skills. Thorough understanding of customer requirements. Proficient in MS Office applications (Outlook, PowerPoint, Excel, SharePoint). Additional Requirements: Willingness to travel domestically (approximately 20%).

Conduct stage-wise inspection during fabrication of: Pressure Vessels Heat Exchangers Fire Heaters with Convection Modules Perform QA/QC services at site , including: Erection and installation of static equipment Inspection and monitoring of piping systems Ensure compliance with project specifications , codes , and quality standards Prepare and maintain inspection reports , NDT records , and QA documentation Coordinate with third-party inspection agencies and client representatives Mandatory Certifications: ASNT SNT-TC-1A Level II in: Liquid Penetrant Testing (LPT) Magnetic Particle Testing (MPT) Radiographic Testing (RT) Ultrasonic Testing (UT) Visual Testing (VT) Preferred Certification: CSWIP 3.1 Welding Inspector (Candidates with this certification will be given first preference) Desired Candidate Profile: Strong knowledge of fabrication codes (ASME, API, etc.) Hands-on experience in inspection and QA/QC documentation Ability to work independently and manage site QA/QC activities Excellent communication and coordination skills Benefits : Competitive salary package Opportunity to work on prestigious Oil & Gas projects Career growth Job Types: Full-time, Contractual / Temporary Contract length: 24 months Pay: ₹16,897.35 - ₹62,830.65 per month Ability to commute/relocate: Bharuch, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): B.E. in Mechanical / Metallurgy / Production Engineering ? Hands-on experience in inspection and QA/QC documentation ? ASNT SNT-TC-1A Level II in: Liquid Penetrant Testing (LPT) Magnetic Particle Testing (MPT) Radiographic Testing (RT) Ultrasonic Testing (UT) Visual Testing (VT) Location: Bharuch, Gujarat (Preferred) Work Location: In person

We have 2 different positions Precast Execution Lead (20+ Years of experience) Precast QC Lead (10+ Years of experience) Qualification: B.E. – Civil Engineering Certifications (if any): PMP/Lean/Six Sigma Preferred Relevant Industry Exposure: Infrastructure Precast Expertise. Building exposure is preferred. International experience is preferred. Technical competencies: Expertise in Construction Methods and Planning for Precast Construction with a long tenure in the industry. Oversee multiple Precast Projects execution to set benchmarks, align resources, track progress, and showcase the Precast Technology benefits in various infrastructure as well as buildings Precast Construction projects across India for all. The role does not include direct execution responsibility but to monitor and catalyse progress. Propose Precast Construction methods as alternates in key ongoing and tender projects to accelerate delivery, improve productivity along with superior quality and safety. Build a robust network of execution resources such as precast vendors, mould manufacturers, accessory suppliers, modern machinery agencies. Align and mobilize execution workforce for production, installation, structural finishing, prestressing/post tensioning to ramp up precast set up quickly and continually improve the time to peak in project execution. Support in developing the overall capacity utilization of Precast related resources such as factories, workforce, moulds, and P&M across the company. Manage and build a team of Production and Installation Engineers along with the flying squads that are deputed to various sites per project needs. Build cross functional capability in the teams for Infrastructure as well as Buildings knowledge and know how. Manage training needs and safety and quality responsibilities to build a high-performance precast execution team known for their Precast expertise. Support in Standardization and Modularization efforts of the company by collecting and analyzing data of IC wide demands and challenges. Support in building innovative data collection and analysis options using IoT and AI

Role Overview: Royal Pharma is seeking a Senior Manager - Production to oversee and manage manufacturing operations at our new API/Advanced Intermediates facility. The candidate will be responsible for ensuring smooth plant operations, production efficiency, compliance, and team leadership to meet business goals. Key Responsibilities: 1. Production Planning & Execution Oversee daily API/Advanced Intermediates production activities, ensuring adherence to schedules and targets. Ensure optimal utilization of resources, manpower, and equipment for cost-effective operations. Troubleshoot production issues and drive process improvements. 2. Compliance & Quality Assurance Ensure production activities comply with cGMP, FDA, WHO, and other regulatory standards. Work closely with QA/QC teams to maintain product quality and resolve deviations. Handle regulatory inspections, audits, and documentation related to production. 3. Safety & Environment Implement and enforce SHE (Safety, Health, and Environment) protocols to maintain a safe workplace. Ensure compliance with effluent management and sustainability initiatives. 4. Process Optimization & Cost Control Drive initiatives to improve yields, reduce costs, and enhance productivity. Implement Lean Manufacturing and Six Sigma practices to optimize production processes. 5. Team Management & Leadership Lead and mentor a team of production supervisors, engineers, and operators. Conduct training programs for team competency development and skill enhancement. 6. Coordination & Reporting Collaborate with R&D, Supply Chain, Maintenance, and Regulatory teams for smooth operations. Prepare reports on production efficiency, downtime, and process improvements. Key Skills & Competencies: ✔ Qualification : B.Tech ( Chemical ) ✔18-25 years experience in API/Advanced Intermediates production and scale-up. ✔ Experience in GMP, FDA, EMA, and EHS regulations. ✔ Problem-solving skills for process troubleshooting and efficiency improvement. ✔ Leadership and team management capabilities. ✔ Strong knowledge of equipment, reactors, and automation in API manufacturing. Location: Boisar, Tarapur- Mumbai/Maharashtra Reporting to: Site Head/Plant Head Experience: 20+ years in API/Advanced Intermediates manufacturing, with at least 10+ years in a managerial role. Qualification: B.E/ B.Tech. / M.Tech in Chemical Engineering or M.Sc. in Chemistry. Industry Pharmaceutical Manufacturing Employment Type Full-time

Job Title: Project Quality Engineer Locations: Pan India & Global Reporting: HOD About Newen Systems Newen Systems is India’s leading power conversion and energy storage solutions provider, driving energy transition and grid stability. Newen’s state of the art manufacturing facilities at Vadodara is at the heart of driving innovation and GW scale energy revolution for the world. With 3,000+ MW of battery storage deployed across 65+ countries in all seven continents, Newen Systems in technical collaboration with Dynapower is delivering BESS, Green H2, Microgrid and e-mobility infrastructure solutions to customers in India and around the world. Newen’s cutting edge energy management system is helping customers maximize their energy investment in ways it was not imagined earlier. Newen is uniquely positioned globally to provide EMS and PCS under one roof enabling customers to do integration tests within the factory rather than on site saving them time and money. As we expand, we are looking for intrapreneurial talent who have the passion to drive energy transition and deliver solutions to drive sustainability on a global scale. Job Summary: The Electrical Project Quality Engineer is responsible for ensuring that all electrical installations and systems meet the required quality standards and comply with applicable codes, standards, and project specifications. This role involves planning, implementing, and monitoring quality control procedures throughout the project lifecycle. Key Tasks: Develop and implement project-specific Quality Plans, Inspection & Test Plans (ITPs), and checklists for electrical systems. Conduct inspections and tests on electrical installations including cable trays, wiring, panels, grounding, lighting, and control systems. Review and verify electrical drawings, specifications, and material submittals for compliance. Coordinate with construction teams, subcontractors, and suppliers to ensure quality standards are met. Monitor and document all quality control activities and maintain comprehensive records. Identify non-conformities, issue NCRs (Non-Conformance Reports), and ensure corrective actions are implemented. Participate in internal and external audits and support continuous improvement initiatives. Ensure compliance with safety regulations and electrical codes (e.g., NEC, IEC, IEEE). Provide technical support and training to site personnel on quality procedures and standards. Skills: Technical Skills: Electrical Engineering Knowledge: Strong understanding of electrical systems, components, and standards (e.g., IEC, NEC, IEEE). Quality Management Systems (QMS): Familiarity with ISO 9001 and other quality frameworks. Inspection & Testing: Proficiency in electrical testing methods (e.g., insulation resistance, continuity, voltage drop). Documentation & Reporting: Ability to prepare and manage ITPs, checklists, NCRs, and quality reports. Standards & Codes Compliance: Knowledge of national and international codes relevant to the project (e.g., MNRE, BIS for solar). Root Cause Analysis: Skills in identifying, analyzing, and resolving quality issues using tools like 5 Whys, Fishbone Diagram, etc. Analytical & Problem-Solving Skills Attention to detail in identifying defects or deviations. Ability to interpret technical drawings and specifications. Strong troubleshooting skills for on-site quality issues Tools & Software MS Office Suite : Especially Excel and Word for documentation and reporting. AutoCAD / Electrical CAD : For reviewing and marking up drawings. Quality Management Software : Tools like SAP QM, ETQ, or custom project management platforms. Testing Equipment : Familiarity with multimeters, insulation testers, and other electrical QA tools. Qualifications & Experience: Bachelor’s degree in electrical/Electronic engineering or related field. Minimum 7 years of experience in electrical QA/QC roles within BESS or industrial projects. Strong knowledge of electrical systems, standards, and testing procedures. Excellent communication, documentation, and problem-solving skills.

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Officer Date: Jul 25, 2025 Location: Ahmednagar - Quality Control Company: Sun Pharmaceutical Industries Ltd Position: Officer / Sr. Officer – Quality Control Grade: G12C / G12B No. of Position: 1 No. Job Location: Ahmednagar Qualification: M.Sc. (Chemistry) Experience: 5 to 9 yrs experience in API manufacturing plant Job Profile To investigate LAB Event, OOS/OOT results, Un-Planned deviation, Planned Deviation in all Section and timely submit for approval. To prepare and review the laboratory investigation report hypothesis study / evaluation study protocol and reports. To review of Analytical data like packing material, In-Process samples, Intermediate samples, Raw material and Finished Product samples, Stability samples etc. To review of instruments log books and other log books like IC Column, LCMS Column and WRS Log books etc. To ensure effective review of physical and electronic raw data and records generated in QC laboratory Review sample set and instrument methods, custom field related activity in Empower 3 software To review Audit trail of laboratory instrument which are connected with software like EMPOWER, LAB X, LAB Solution etc. To co-ordinate and conduct self inspection (internal audit) and its compliance To execute and review change control proposals in TRACK WISE. To monitor the compliance with the requirements of Good Manufacturing Practice and Good laboratory practice. To participate in management reviews of process performance, product quality and of the quality management system and advocating continual improvement. To ensure a timely and effective communication and escalation process exists to raise quality issues to appropriate levels of management. To conduct training program and ensure its effectiveness To Co-ordinate and manage with other department of the plant to build continuous quality in product and systems with technical support to get customer satisfaction. To co-ordinate with contract laboratory and full fill the requirements as per responsibilities section in technical / quality agreement and extend support as per requirements. Apply Now » Apply Now Start applying with LinkedIn Please wait...

Job Overview We are looking for an experienced and detail-oriented Quality Engineer to manage and ensure the quality of construction and installation activities for Water Supply, STP, and WTP projects at our Jabalpur site. The ideal candidate will be responsible for implementing quality control systems, conducting site inspections, and ensuring compliance with standards and specifications. Key Responsibilities Implement and monitor Quality Assurance (QA) and Quality Control (QC) plans at the project site. Conduct inspection and testing of civil, mechanical, and electromechanical work at each stage of construction. Ensure materials, workmanship, and processes comply with contract specifications, IS codes, and CPHEEO guidelines. Prepare and maintain all QA/QC documentation including checklists, inspection reports, and test reports. Coordinate with execution teams, contractors, and third-party inspection agencies. Identify and report non-conformities and ensure corrective/preventive actions are implemented. Maintain records of material approvals, lab test reports, and site observations. Assist in internal audits and quality reviews. Provide training and guidance to site teams on quality standards and best practices. Qualifications Qualification: B.E./B.Tech in Civil Industry: Infrastructure / Water Supply / STP / WTP / EPC Projects Joining: Immediate Joiners Preferred Additional Information Key Skills & Competencies Strong understanding of QA/QC procedures, testing methods, and material specifications. Familiar with civil and mechanical work inspection for STP, WTP, and pipeline projects. Knowledge of IS codes, CPHEEO manual, and third-party testing protocols. Excellent attention to detail, record-keeping, and communication skills. Proficient in MS Office and quality management systems. Preferred Experience Experience in government/urban infrastructure projects involving water treatment or distribution. Exposure to NABL/TPA coordination and RMC/construction material testing.

About The Job About ProcDNA ProcDNA is a global consulting firm. We fuse design thinking with cutting-edge tech to create game-changing Commercial Analytics and Technology solutions for our clients. We're a passionate team of 275+ across 6 offices, all growing and learning together since our launch during the pandemic. Here, you won't be stuck in a cubicle - you'll be out in the open water, shaping the future with brilliant minds. At ProcDNA, innovation isn't just encouraged, it's ingrained in our DNA. What We Are Looking For Clinical Database Programmer with a solid understanding of Clinical Protocol, Medical and Scientific Principles of conducting clinical trials. We are seeking an individual who not only possesses the requisite expertise but also thrives in a fast-paced environment. What You’ll Do Design the eCRF layout and the database corresponding to the eCRFs to hold the data from the EDC system and Setup Core Configurations. Implementing the Dynamic rules as per the Sponsor requirements. Create, test, and maintain trial-specific plausibility and consistency Edit Checks as per Data Validation Specification. Analyze complex checks and Develop Custom Functions using C# for Rave studies or other EDC. Incorporate internal feedback and update programs as required. Incorporate Sponsor Acceptance Testing (SAT) feedback. Maintain and update the eCRFs and their components as required for protocol amendments or required metadata updates. Perform second/final review for peer deliverables. Create RAVE System Configuration Specification (Core config, Report Config, e-learning config, Appendix config & coding spec in RAVE or other EDC). Incorporate RAVE Configuration Specification. Facilitate Internal Configuration Review Meeting (ICRM). Revise and update eCRF booklet, DVS and Configuration Specification. Facilitate Sponsor Acceptance Meeting (SAM). Handle issues related to QC/UAT/PROD and tracking issues to closer. Review of the DVS for clarity and to ensure checks are consistent and appropriate based on eCRF design. Provide feedback to DVS author. Support CRO trial activities, including CRF annotation, database setup, specification generation, Clinical view settings, and dataset comparison. Create reports as per the Sponsor specification document using JReview, SAS, BOXI. Estimate and perform migration process for Post Go-Live studies (handling RFCs). Performe DB Coordinator role for multiple trials. Mentor new hires in CRO and EDC activities. Must Have Protocol reading and understanding Expertise in ‘Critical Data Point Strategy (CDPS) or SDV’ implementation. Scientific background: A solid understanding of Clinical Protocol, medical and scientific principles of conducting clinical trials. Strong writing and communication skills: The ability to clearly articulate and concisely explain complex information. Research and analytical skills: Ability to gather, interpret, and synthesize data into insightful information. Attention to detail: Ensuring accuracy and adherence to guidelines such as Protocol, Specification, Library Standards, ICH GCP, etc. Project management skills: Managing the document development process and meeting timelines. People management skills: Managing the team of highly qualified individuals (applicable for Team Lead role only). Certified Medidata Study Builder (SDBE), Oracle - InForm/ Central Designer, Veeva Studio B.E./B.Tech - Computer Science-based courses or Circuit Branches) M.Sc./ MCA in the stream of Computer Science B.Sc./ BCA in the stream of Computer Science) Why Join Us? Be part of a fast-growing consulting firm making a real impact in the healthcare space. Work directly with leadership and stakeholders. Own and shape the marketing strategy, with full freedom to innovate and experiment. Locations we are currently hiring for this role: Pune, Gurgaon, Bangalore, Kochi, Hyderabad, Chennai Skills: database management,dynamic rules implementation,project management,central designer,plausibility and consistency checks,veeva studio,critical data point strategy (cdps),report generation (jreview, sas, boxi),attention to detail,data validation specification,edc systems,research and analytical skills,clinical protocol,ecrf layout design,rave studies,people management,clinical database programming,strong writing and communication,c# programming,medical and scientific principles,post go-live studies migration,oracle inform,protocol understanding

Job Description Maintain media stock and reconcile records of media used in analysis. Perform water sampling and analysis following defined SOPs/protocols and ensure proper documentation. Report and log OOS (Out of Specification), OOT (Out of Trend), and EM (Environmental Monitoring) excursions. Conduct environmental monitoring of the laboratory. Perform analytical validation, culture maintenance, and growth promotion testing (GPT) of media; record observations and generate reports. Carry out microbiology laboratory tests such as Bioburden Analysis, MLT (Microbial Limit Test), Sterility Testing, BET (Bacterial Endotoxin Test), etc., in compliance with approved procedures. Skills And Proficiency Microbiology Instrumentation Handling – Expert Good Laboratory Practices (GLP) & Documentation Accuracy – Practitioner Data Integrity & Documentation – Practitioner Regulatory Compliance – Practitioner SOP Preparation & Revision – Practitioner BET & Sterility testing expertise and evaluation skills – Expert Interpretation of Resulting Data Trend – Practitioner Laboratory Instrument qualification, Calibration & Maintenance – Practitioner Quality Control & Compliance – Practitioner QMS Documentation (OOS, OOT, Deviation & Incident) – Beginner CAPA, Deviation, and Change Control Management – Beginner

Job Title : Customer Relationship Manager Department: Commercial Key Responsibilities: · Adhere to organisational processes, protocols, and compliance standards in day-to-day operations. · Attend client calls regularly and act as the primary point of contact, ensuring smooth communication and coordination from project initiation to final execution. · Resolve customer complaints promptly and effectively, ensuring high levels of customer satisfaction and retention. · Make follow-up calls to clients for pending payments and AMC (Annual Maintenance Contract) renewals to ensure timely collections and contract continuity. · Coordinate with clients for timely document collection and obtain confirmations for necessary arrangements under the client's scope. · Coordinate with internal teams from project initiation to completion to ensure timely and successful project execution. · Responsible for maintaining data in software as per the requirements. · Sample collection and report generation for QC Lab. Minimum Requirement: A graduation in any discipline is mandatory 4-5 yrs of proven experience working in a CRM role or similar. Proficiency in MS Office is mandatory. Strong communication, coordination, and project management skills.

Job Title: Quality Assurance (QA) Executive – Café Operations Location: Bangalore Department: Quality & Compliance Reporting To: Quality Manager / Area Manager Job Purpose: To ensure that all café outlets operate in compliance with food safety standards, hygiene protocols, and company-set quality benchmarks by conducting regular audits, training staff, and initiating corrective actions. Key Responsibilities: Conduct periodic quality and hygiene audits across cafés. Monitor compliance with FSSAI and other applicable food safety regulations. Ensure adherence to standard operating procedures (SOPs) in food handling, preparation, and storage. Report quality deviations and follow up on corrective and preventive actions (CAPA). Conduct food safety training and refresher sessions for café staff. Perform vendor audits and ensure raw material quality standards are maintained. Maintain documentation related to QA inspections, certifications, and hygiene checks. Assist in implementing new quality control processes and initiatives. Key Skills Required: Strong knowledge of food safety standards (FSSAI, HACCP, ISO 22000). Good observation and audit skills. Strong documentation and report-writing ability. Basic understanding of café or QSR operations. Ability to travel extensively across café locations. Qualifications: Bachelor’s/Master’s degree in Food Technology, Microbiology, Hospitality, or a related field. 1–3 years of experience in a QA/QC role within the food industry, preferably in QSR, café chains, or hospitality sector. Additional Requirements: Willingness to travel to multiple café outlets as part of regular audits. Good communication skills to train and guide store-level staff. Proficient in MS Office (Excel, Word, PowerPoint).

We are looking for the following positions for our sandwich puf panel manufacturing industry in Palladam, Tirupur Quality Control -5 nos Qualification: ITI, Diploma any graduate. Experience:0-2 years. Location: Palladam, Tirupur Job Type: Full-time Pay: ₹15,000.00 - ₹25,000.00 per month Benefits: Commuter assistance Health insurance Provident Fund Ability to commute/relocate: Palladam, Tamil Nadu: Reliably commute or planning to relocate before starting work (Preferred) Education: Diploma (Preferred) Experience: QC manufacturing industry: 1 year (Preferred) Work Location: In person

Data Specialist Join Forage AI as a Data Specialist -Technical QA. If you’re a detail-oriented, tech-savvy professional who loves working with data, then this may be the right role for you! You’ll collaborate with our talented team of engineers who are working at the bleeding edge of data science and data automation. Responsibilities: Our technical data specialists play an integral role in ensuring that our clients consistently receive high-quality datasets in a timely manner. You will collaborate with our dev team to ensure the end-to-end completion of the 'Extraction-QA-Feedback-Delivery’ process. You will meet our end goal of ensuring that our clients receive carefully curated datasets that are customized and structured as per their requirements. Here’s what you’ll do: ● Extract, QC, audit, and deliver completed and approved datasets meeting predetermined deadlines with a goal of complete accuracy. ● Research and troubleshoot issues associated with data and/or tools provided. ● Catch and report bugs by highlighting trends and exceptions that require fixes. ● Suggest process improvement ideas that will bring efficiency and structure to workflows. ● Implement automation solutions to make our QA processes more robust and efficient. ● Work closely with our team of developers to manage ETAs and deliverables ● Assist our AI and RPA models by manually parsing data for delivery or process automation. ● Conduct domain-specific preliminary research for building subject matter expertise ● Own end-to-end operations process for your daily project deliverables. ● Respond to client inquiries related to ongoing projects. ● Be a culture carrier and live by all of our core values. Requirements: ● Must have at least a bachelor’s degree in any field. ● Must have worked on Excel / Google Sheets for at least 1 year. ● Familiarity with XPath, SQL, or any query/coding language would be a plus. ● Excellent attention to detail and proven ability to perform under pressure. ● A quick learner with a strong analytical mindset who is tech-savvy and enjoys working with data. ● An open-minded, motivated self-starter with a positive approach to problem-solving. ● An active listener who can effectively translate instructions into action. Other Infrastructure Requirements: Since this is a completely work-from-home position, you will also require the following - ● High-speed internet connectivity for video calls and efficient work. ● Capable business-grade computer (e.g., modern processor, 8 GB+ of RAM) ● Dedicated workspace (at home) for uninterrupted and efficient work. ● Headphones with clear audio quality. ● Stable power connection and backups in case of internet/power failure. Additional Information: ● While we do have separate teams for AI & ML, this job does not guarantee an organic segue into these roles. ● This is not an opportunity to develop a career solely in data visualization.

Data Specialist Are you an enthusiastic extrovert with a high passion for performance? Do you enjoy working in teams to achieve a common goal together? Do you love solving problems and enjoy working through challenges? Is multitasking one of your strengths? If so, then join Forage AI as a Data Specialist! Responsibilities: ● Develop, QC, audit, and deliver completed and approved datasets meeting predetermined deadlines with a goal of complete accuracy. ● Develop process improvement ideas that will bring efficiency and structure to workflows. ● Assist our AI and RPA models by manually parsing data to help derive insights for automation. ● Interpret and understand client requirements for every project and execute it per the defined rules. ● Perform annotations to help train our ML models. ● Direct and monitor the progress and performance of the team. ● Act as a culture carrier and live by all our core values of ownership, commitment, collaboration, agility and innovation, and a growth-oriented mindset. ● Respond to client inquiries related to ongoing projects. ● Research and troubleshoot issues associated with the data and tools provided. ● Assess project proposals, provide time estimates then document time and accuracy for evaluation purposes. ● Assist in documentation and continual improvements of SOPs for internal workflows. ● Prepare tools and reports that measure and evaluate team accuracy and productivity. ● Assist in planning and allocation of daily work queues. Requirements: ● Must have a bachelor's degree in any stream. Degrees in commerce, statistics, or finance would be preferred. ● They must have proficiency in Advanced Excel. ● Must have at least 2-3 years of work experience. This can include - ○ any role that involved building high-quality datasets, or ○ operations roles that may have involved managing business processes, audits, etc., or ○ some exposure to client management, including gathering requirements to build datasets customized according to our client’s needs. ● Preferred experience as a Data Quality Analyst and working with large data sets. ● A solid understanding of financial investment markets, private equity, or equity research would be an added advantage. ● Must have high integrity, a robust data-oriented mindset, excellent Business communication (written and verbal) skills, and a sincere approach to work. ● Must be able to pay excellent attention to details and have good change management skills. ● Must be a team player and a quick learner with a solution-oriented nature and a positive attitude. Other Infrastructure Requirements: Since this is a completely work-from-home position, you will also require the following - ● High-speed internet connectivity for video calls and efficient work. ● Capable business-grade computer (e.g., modern processor, 8 GB+ of RAM, and no other obstacles to interrupted efficient work). ● Headphones with clear audio quality. ● Stable power connection and backups in case of internet/power failure.

Job Title - Site Quality Head - API Job Grade : GM / Sr.GM Location : Ahmednagar At Sun Pharma, we commit to helping you “ Create your own sunshine ”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Position Summary – Ensure the supply of high quality, GMP compliant products, define operational strategy for quality system management at site, finalize site quality assurance and quality control goals, objectives and strategies in line with Sun Pharma compliance, product quality management objectives and regulatory requirements. Provide leadership and direction to ensure achievement of all site accountabilities for QA, QC and Stability at site. Proactively assess quality issues at site and ensure compliance to QA/QC regulatory requirements in manufacturing operations at the site and track quality assurance/control metrics with site manufacturing and drive them down. Assure all time readiness of site for regulatory agency inspections\internal audits at any given point The incumbent will assure individual compliance with the all concerned regulatory requirements, GxP’s and applicable department programs, including training, documentation, Standard Operating Procedures, and Sun Pharma Global Quality Policies, Standards and Procedures. Key Responsibilities Assess quality issues at site and ensure compliance to QA/QC regulatory requirements in manufacturing operations at site and track quality metrics with site manufacturing management and drive them down. Accountable for designing/implementing and ensuring compliance to all quality related SOPs, Policies, Standards and Quality systems at the site Design and execute continuous improvement initiatives at the site to enhance compliance, drive efficiencies and cost effectiveness. Responsible for ensuring availability of adequate resources, including manpower to maintain compliance with GXP requirements. Facilitate harmonization and consistent implementation of Quality Systems and procedures at site, in alignment with Global Quality policies\standards. Ensure market complaints, failures, deviations are investigated and corrective and preventive actions are implemented with adherence to timelines Assure all time readiness of site for regulatory agency inspections\internal audits and appropriate implementation of corrective actions regarding observations made by the agencies\internal audit teams Monitor industry trends/issues faced internally and identify scope for improving Site quality management and processes. Ensure compliance to regulatory requirements on product, process and release procedures. Prepare site quality revenue and capital budgets and headcount projections, track and manage expenditures and headcount to budget over the fiscal year. Ensure release of safe and effective drug products from site as per cGMP requirement and regulatory commitment. Responsible for ensuring smooth collaboration with all Sun Pharma sites and functions to leverage synergies. Follow the EHS policy, laboratory standard operating procedures and maintain the compliance to GMP requirements Educational Qualification B.Pharm / M.Pharm Experience Tenure : 20 to 22 Yrs Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!

COMPANY - Leading Apparel MNC POSITION - General Manager Merchandising LOCATION - India SALARY - Open Job Summary: We are seeking a seasoned and strategic General Manager – Merchandising with direct experience working with the UNIQLO brand to lead our end-to-end merchandising and product execution function. The successful candidate will bring deep knowledge of UNIQLO’s product philosophy, operational rigor, and global merchandising standards. This role is critical to driving our performance as a trusted manufacturing partner, ensuring exceptional service, efficient execution, and product excellence. Key Responsibilities: 1. UNIQLO Account Management Serve as the primary liaison for UNIQLO teams on all merchandising, development, and planning matters. Understand and execute against UNIQLO’s strict quality, price, and timeline requirements. Ensure full compliance with UNIQLO's SOPs, compliance standards, and production systems (e.g., SMV, costing, traceability, etc.). 2. Product Development & Merchandising Lead development of seasonal collections and core product lines in collaboration with internal design, technical, and sourcing teams. Guide pricing strategies, product positioning, and cost engineering in line with UNIQLO expectations. Translate trend direction and buyer inputs into executable product plans with detailed tech packs and timelines. 3. Manufacturing & Supply Chain Coordination Work cross-functionally with production, QA/QC, sourcing, and raw material procurement teams to ensure efficient product execution. Drive lead time optimization and ensure 100% on-time delivery (OTD) across all UNIQLO orders. Ensure product development aligns with manufacturing feasibility and cost efficiency. 4. Data & Performance Analysis Track order performance, development accuracy, and cost margins with precision. Analyze customer feedback, sales performance (if available), and factory output to refine merchandising strategy. Lead product risk assessment and issue resolution proactively. 5. Team Leadership & Development Build, mentor, and lead a team of merchandisers, coordinators, and product managers. Create a culture of accountability, speed, and precision consistent with UNIQLO’s operational DNA. Facilitate ongoing training in UNIQLO systems, processes, and quality requirements. Qualifications & Experience: 12+ years of experience in apparel merchandising, with a strong background in handling UNIQLO accounts either directly or as part of a vendor team. Proven success managing large-volume accounts with strict timelines and high quality standards. Strong understanding of product lifecycle management, costing, and bulk production processes. Experience in working with Japanese buyers or global buying offices preferred. Bachelor's degree in Apparel Merchandising, Fashion Management, Business, or related field.

JOB SUMMARY The Quality Assurance Manager in a TIC organization is responsible for maintaining and improving the Quality Management System (QMS) to ensure compliance with industry standards, regulatory requirements, and customer expectations. This role involves overseeing testing, inspection, and certification processes to ensure consistent, accurate, and reliable services, while driving continuous improvement initiatives within the organization. The Quality Assurance Manager has direct access to the Head of Operations and to the highest level of Management at which decisions are made regarding laboratory policy or resources. DUTIES, RESPONSIBILITIES AND AUTHORITIES Data Analysis and Reporting : Monitor quality performance metrics (e.g., non-conformities, Client complaints, audit findings) and provide regular reports to senior management. Perform root cause analysis on every client complaint and create processes to prevent repeated issues from occurring. Use data analysis to identify trends, areas of improvement, and opportunities for risk mitigation. Client Relations : Serve as a liaison with customers regarding quality-related concerns. Ensure client feedback is addressed through corrective actions and that their quality requirements are met consistently. 3. Quality Management System (QMS) Develop, implement, and maintain the QMS in line with ISO/IEC 17025, ISO 9001, and other relevant standards. Ensure all procedures, work instructions, and forms are up to date, followed, and meet regulatory and customer requirements. Lead internal and external audits, including accreditation body audits and customer audits. Audit test reports, survey reports and any other type of reports on a random and continuous basis. Serves as the focal point for QA/QC activities and is responsible for the oversight and/or review of quality control data. Function independent from any of the operations for which she/he has quality assurance oversight. Hold documented training and/or experience in QA/QC procedures and is knowledgeable in the quality system, as defined under NDELCP QA requirements. Has general knowledge of the analytical test methods, survey knowledge and other background information for which data review is performed. Regulatory Compliance Ensure compliance with relevant national and international regulations related to testing, inspection, and certification services. Monitor changes in regulations and standards, ensuring the organization remains compliant. Work closely with accreditation bodies to maintain certifications and accreditations. Continuous Improvement Lead continuous improvement initiatives aimed at enhancing the accuracy, efficiency, and reliability of testing, inspection, and certification services. Implement corrective and preventive actions (CAPA) to address non-conformities, customer complaints, and other quality issues. Foster a culture of continuous improvement and quality excellence within the organization. Audit Management : Plan and conduct internal audits to evaluate the effectiveness of the QMS. Coordinate with external auditors for accreditation and certification audits. Ensure audit findings are addressed promptly, and corrective actions are implemented. Can evaluate data objectively and perform assessments without outside (e.g., managerial) influence. Arranges for and conducts internal audits. Notifies management of deficiencies in the quality system and monitors corrective actions. Document Control Oversee document control procedures to ensure the proper creation, review, approval, distribution, and archiving of quality-related documentation. Manage the central repository of quality documents and ensure accessibility for relevant personnel. Training and Development Develop and deliver training programs on quality standards, policies, and procedures to staff involved in testing, inspection, and certification activities. Ensure staff competency through ongoing evaluations and skill development. KEY TASKS 1. Preventive risk mitigation should be performed on every process. 2. Client complaints will be priority and need to be addressed urgently. Root cause analysis of all problems should be carried out in a timely manner so that the complaints can be immediately addressed. New process creation and implementation by working with different vertical heads should be carried out in a timely manner. 3. Responsible for timely, accurate and highest quality services 4. Oversee the ISO certification process and procedures 5. Be responsible for maintenance of records, test procedures and update files accordingly 6. Be responsible for the Quality in the lab along with the Lab Managers 7. Oversee round robin testing, 3rd party testing to ensure quality 8. Be responsible for overseeing lab technicians/ supervisors etc. Provide resources for training 9. Be flexible based on the company's needs in terms of duties 10. Be willing to test and offer opinion on new software services Qualifications · Bachelor’s degree, Quality Management, or a related field. · (5+ years exp) in a quality management role within the TIC industry or a related sector. · In-depth knowledge of ISO/IEC 17025, ISO 9001, and other relevant standards. · Experience managing internal and external audits. · Strong understanding of regulatory compliance requirements for testing, inspection, and certification services. · Proficiency in quality management software and data analysis tools. COMPETENCIES 1. In-depth Knowledge of Relevant Standards 2. Regulatory Compliance 3. Quality Management Systems (QMS) Expertise 4. Auditing and Inspection Skills 5. Continuous Improvement & Problem Solving 6. Risk Management 7. Data Analysis and Reporting 8. Attention to Detail 9. Leadership and Team Management 10. Communication and Stakeholder Management JOINT ACCOUNTABILITIES: 1. Be willing to travel if needed to implement Quality process in different locations as needed. 2. Jointly responsible for collaborative work with members of the Group’s business to achieve the Group’s vision. 3. Jointly responsible with Group’s operational team to ensure an atmosphere of learning, R&D, quality focus and regulatory compliance. Job Types: Full-time, Permanent Pay: ₹50,000.00 - ₹100,000.00 per month Benefits: Health insurance Paid sick time Paid time off Provident Fund Schedule: Monday to Friday Ability to commute/relocate: Tambaram, Chennai, Tamil Nadu: Reliably commute or planning to relocate before starting work (Required) Experience: Quality management: 5 years (Required) Language: English (Required) Work Location: In person

Job Profile Overview : Experienced Quality Control Engineer with a strong background in stage-wise inspection of pressure equipment as per QCP and approved drawings. Proficient in preparing inspection reports, RT/PT evaluations, and maintaining material traceability and welder records. Skilled in coordinating with NDE vendors, handling ASME/ISO audits, and driving continual improvement initiatives. Adept at MIS reporting, root cause analysis, and ensuring compliance with safety and quality standards. Qualification : B.E/ B.tech Mechanical Engineering Experience : 5-8 year’s experience in Pressure vessels, Heat Exchanger, structure items (Platform, skid, railing, staircase, etc.) Accountable & Responsible for: 1) To carry out Stage wise inspection (Welding, fit up, Dish end Inspection, Nozzle, PT Examination, final visual & dimensional inspection, Pressure testing, EP, Drain ability etc.) as per approved drawing & QCP. 2) Prepare Inspection report and keep report (Hard & Soft) in respective folder / file. 3) Prepare MIS (Management Information System) reports and submit them to the reporting manager. Monthly Rework / Rejection data Monthly Deviation report RT summery sheet External Customer complaints 4) Review and approve stamp transfer for Welder no. & Joint no. near welding for all equipment's (Pressure parts only). 5) Prepare RT Request sheet & Coordination with NDE Vendor. 6) Review RT Examination Film & Report. 7) To prepare equipment wise RT Examination summery sheet. 8) Prepare Material History chart and arrange Test certificate. 9) To arrange Quality dossier as per Index and submit to reporting manager for review & approval. 10) To Perform PT examination & prepare report. 11) Provide as built dimension to design team for as built drawing preparation. 12) Arrange Stage wise Photographs for Equipment – PT Examination, Pressure testing, Pre-dispatch, RA (surface finish) and keep at Respective Project folder. 13) Review the WPS / PQR / WPQ monthly & update if any additional requirement. 14) Prepare welder Continuity record & update in file. 15) Prepare & display qualified welder list for every 3 month and distribute it to Production. 16) Assign welder no. & entry in welder list. 17) Arrange test coupon for new welder & qualification done as per procedure. 18) Involve in safety activities and update unsafe condition & activities to respective team. 19) Do root cause analysis along with corrective action with Production team on Rework / Rejection and Deviation. 20) Conduct meeting with Welder, Fitter & shop supervisor and discuss Deviation / QC observation. 21) Provide Technical support to QA & projects. 22) Implement continual improvement tools. 23) Support to other unit’s engineers for Quality related activities. 24) Prepare daily & weekly planning of pending works and discuss with reporting manager for priority allocation. 25) Involve in ASME U & R stamp equipment. 26) Involve in ASME U & R stamp audit and face External audit. 27) Involve in ISO 9001 2015 activities and face External & internal audit. 28) To maintain the 5S at Shop & Office. 29) KRA / KPI monitoring & achieving as per given targets. Technical Skills : Knowledge of Basic Quality Tools, GDP, ASME U stamp, CE marking Behavioral Skills : Communication, Leadership, Work Planning Skills Computer Literacy : MS Office Key Purpose : To assure the product quality as per standards.

We are seeking an accomplished Senior Managerial position of QAQC & Operational Excellence to establish, lead and continuously elevate our Quality function across system quality, supply quality and field quality for utility‐scale renewable energy projects. Located in our Pune head office, you will architect and institutionalize a world‐class QA & QC department defining policies, processes and metrics and ensure EPC partners deliver defect‐free, compliant, high‐performance assets. Your zero‐compromise mindset for quality, coupled with deep expertise in quality management systems and operational excellence frameworks, will be critical to our ambition of setting new benchmarks in India’s clean‐energy sector. Key Responsibilities 1. Department Setup & Governance Organizational Design: Define the QA & QC department structure, roles & responsibilities, reporting lines and resourcing plan aligned to project pipeline. Quality Framework: Develop and deploy an Integrated Management System (IMS) encompassing ISO 9001, ISO 14001, ISO 45001 and industry‐specific standards. Policies & Procedures: Author and maintain Quality Manual, Project Quality Plans (MQAP), Field Quality Plans (FQAP), Inspection & Test Plans (ITP), work instructions, checklists and method statements. Governance Cadence: Establish management review forums, steering committees and KPIs for continuous oversight and strategic alignment. 2. System Quality Management IMS Leadership: Drive certification and continual improvement across QMS, EMS and OHSMS; lead internal, external and third-party audits, and close gap findings. MIS & Reporting: Implement a digital Quality Management Information System to track non-conformances, corrective actions, COPQ (Cost of Poor Quality), supplier performance and KPI dashboards for executive review. Risk Management: Facilitate process‐based risk assessments (FMEA, HAZOP), incorporating quality risk controls into project lifecycle and change‐management processes. 3. Supply Quality Assurance Vendor Qualification: Define criteria for A/B/C‐class components (PV modules, inverters, transformers, trackers, balance‐of‐system) and manage vendor audits, capability assessments and approval matrices. Inspection Strategy: Develop an optimal mix of in-house and third-party inspections (FAT, pre-dispatch checks, MDCC) to ensure zero‐defect deliveries. Supplier Development: Partner with procurement and engineering to drive cost-effective quality improvements, PPAP/APQP rollouts, and vendor corrective‐action closure. 4. Field Quality Control Site Quality Oversight: Deploy FQAP, method statements and inspection checkpoints for civil, mechanical, electrical and SCADA works; enforce work‐permit compliance and safety interfaces. Non-Conformance Management: Oversee NCR logging, root-cause analyses (8D/PDCA), corrective/preventive actions and lessons-learned integration into process revisions. Commissioning Readiness: Collaborate with project teams to validate critical-to-quality points, ensure completion of pre-commissioning checks and support handover to O&M. 5. Operational Excellence & Continuous Improvement Lean Six Sigma Deployment: Lead Black Belt/Green Belt initiatives targeting COPQ reduction, productivity gains and process cycle‐time compression across projects. Business Excellence Frameworks: Establish strategic priorities (SP/SI), and functional initiatives (FP/FI), ensuring cascading through KRAs for individual performance alignment. Benchmarking & Analytics: Institute KPI benchmarking (yield, uptime, waste, rework), conduct time-motion studies and apply SPC to monitor process capability. 6. Leadership & Stakeholder Engagement Cross-Functional Collaboration: Act as the quality evangelist with Engineering, Procurement, Construction and O&M teams to embed quality‐by‐design principles. External Interface: Represent the company in regulatory, lender and insurer quality audits; liaise with TPAs, certification bodies and industry forums to influence best practices. Team Development: Recruit, mentor and upskill a high-performing QA & QC team; drive a culture of ownership, innovation and zero‐tolerance for substandard work. Qualifications & Experience Education: Bachelor’s or Master’s in Mechanical/Electrical/Civil Engineering or equivalent; advanced certification in Quality (Six Sigma Master Black Belt, ASNT Level II, Lead Auditor IMS) is highly preferred. Experience: 15+ years in QA & QC and Operational Excellence roles within large-scale renewable energy or power‐generation projects (solar PV, wind, BESS, green hydrogen) in Construction team. Proven track record establishing quality functions and processes de novo, managing end-to-end system, supply and field quality across multiple EPC contractors. Hands-on expertise in ISO 9001/14001/45001, APQP/PPAP, ITP/FAT protocols, NCR management, COPQ frameworks and Lean‐Six Sigma deployments. Technical Skills: Proficiency with QMS software, ERP modules, Microsoft Project/Primavera and BI tools (Power BI preferred). Strong command of industry standards (IEC, IS, ASME, NACE, SSPC) and statutory compliance mandates . Core Competencies Strategic Vision & Execution: Ability to translate executive quality objectives into robust processes and measurable outcomes. Analytical Rigor: Data-driven decision maker with exceptional problem-solving and statistical analysis skills. Influence & Communication: Persuasive leader, adept at stakeholder management—from shop-floor teams to board-level presentations. Safety & Integrity: Unwavering commitment to HSE excellence and ethical practices; fosters a culture of accountability. Change Leadership: Skilled in driving organizational transformation, overcoming resistance and institutionalizing continuous improvement. Location: Corporate Office, Pune Reporting To: Head- Construction & Projects