384 Iso Documentation Jobs - Page 13

Were Hiring: Civil Quality Engineer – Solar Ground Mount Projects Location: Saraipalli, Dist.- Mahasamund, Chattisgarh (Near Raipur) Experience: 3–4 Years Industry: Renewable Energy | Solar EPC Availability: Immediate Joiners Preferred Are you a detail-oriented civil professional with a passion for quality and sustainability? Join our dynamic solar EPC team as a Civil Quality Engineer and help us deliver excellence in ground-mounted solar projects. Key Responsibilities: • Implement and monitor Quality Assurance & Quality Control (QA/QC) procedures for all civil activities on-site. • Conduct inspections for Foundation, Building, Piling, RCC works, Cable trenching, and other civil works. • Review and verify civil work against design specifications, technical drawings, and standards. • Maintain quality documentation including RFIs, checklists, test reports, and non-conformance reports. • Liaise with third-party labs for material and field testing (soil, concrete, aggregates, etc.). • Conduct root cause analysis and implement corrective actions for quality deviations. • Train site supervisors and contractors on civil quality standards and procedures. • Ensure compliance with safety, environmental, and regulatory norms. Desired Candidate Profile: • Diploma / B.E. / B.Tech in Civil Engineering. • Minimum 3 years of experience in quality control for solar ground mount or infrastructure projects. • Strong knowledge of civil construction standards (IS Codes), QA/QC processes, and material testing. • Proficiency in MS Office, AutoCAD, and quality management tools. • Will be posted at Project Site on permanent basis. What We Offer: • Opportunity to work on large-scale renewable energy projects. • Growth-oriented environment with industry-leading practices. • Competitive salary, travel allowances, and accommodation (for site roles). Apply Now: Send your resume to hr@kslcleantech.com

Roles & Responsibility :- Processes adequacy review of each process of the QMS with functions Site visits for QA audit, including Stores Audits Internal Audits every quarter in Bangalore Internal Auditors training program in Bangalore Review of Project Management Plans and Design Management Plans Preparation and updation of Project Quality Plans Monthly report system from each Site Fortnightly QA training for the Site QA persons Monthly QA review meetings External Audit preparations Risk tables updation with each department Preferred candidate profile Any Engineering Graduate with 2-6 years in Quality Exposure to working in Projects environment QMS training , at least as Internal Audit Quality certification such as ISO 9001 Lead Auditor, IRCA, or equivalent is preferred. Experince in Railways or Infrastructure preferred Detail-oriented with strong analytical and problem-solving skills. Proficient in Microsoft Office (Word, Excel, PowerPoint). Ability to work independently and manage multiple audits simultaneously.

Purchase Executive should have Local/Overseas market/supplier base procedure for procurement of material handling standard Inventory Management Product & manufacturing process/specifications Drawing interpretation BOM & Non BOM items. Required Candidate profile Purchase Executive should lnow Steel, Castings, machining & fabrication processes & Quality tools like 8D, PPAP Conversant with ERP system (SAP) for PO generation Contract management

responsible for Quality (Supplier Quality, Product Quality, Customer complaints), manage Audits(IATF, Customer, supplier, process etc) Product / Process improvements through Kaizen. Compliances to 5S & Safety.

1. Quality Management System (QMS) Implementation - Develop, implement, and maintain the companys QMS in compliance with ISO Standards - Conduct internal audits to ensure adherence to QMS procedures. 2. Documentation & Control - Review and approve supplier/vendor QA documents. - Ensure traceability and documentation of materials, welding activities, NDT reports, and inspection logs. 3. Supplier & Vendor Evaluation - Conduct QA audits and assessments of vendors, subcontractors, and suppliers. - Review and verify vendor quality documents, manufacturing records, and material test certificates (MTCs). - Ensure all bought-out items comply with technical and quality standards. 4. Compliance & Codes - Ensure compliance with national and international codes and standards such as ASME, PED, API, ASTM, ISO, and client specifications. - Support compliance during audits by third-party inspection agencies (TPIs) and clients. 5. Non-Conformance & Corrective Actions - Identify, document, and track non-conformities (NCRs) and issue corrective/preventive actions (CAPA). - Follow up on close-out of NCRs and ensure root cause analysis is carried out effectively.

Job Title: Quality and Regulatory Manager (Medical Devices) Reports to: Director of Quality / Head of Operations Job Summary The Quality and Regulatory Manager is responsible for ensuring that all medical device products comply with global regulatory requirements (e.g., US FDA, EU MDR, ISO 13485), maintaining effective quality management systems, and facilitating successful regulatory submissions. The role involves leading internal and external audits, managing documentation, and supporting cross-functional teams to ensure the safety, efficacy, and compliance of medical devices throughout the product lifecycle. Key Responsibilities Quality Management System (QMS): Develop, implement, and maintain the QMS in accordance with ISO 13485, FDA 21 CFR Part 820, and other applicable regulations. Lead internal and external audits, and manage corrective and preventive action (CAPA) processes. Ensure proper documentation, control, and retention of quality records and regulatory files. Oversee product nonconformance investigations and ensure timely closure of deviations. Regulatory Affairs: Prepare, compile, and submit regulatory filings (510(k), CE Mark Technical Files, etc.) for new and existing products in global markets. Monitor and interpret global regulatory changes, ensuring the company remains in compliance. Serve as primary contact for regulatory agencies and notified bodies during inspections and audits. Develop and maintain product registration dossiers and technical documentation. Risk Management: Lead risk management activities in accordance with ISO 14971, including hazard analysis and post-market surveillance. Support product recalls, field safety corrective actions, and complaint investigations. Training & Continuous Improvement: Train and mentor staff on quality and regulatory requirements. Drive continuous improvement initiatives for product and process quality. Cross-Functional Support: Collaborate with R&D, Manufacturing, Supply Chain, and Marketing to ensure compliance in product design, labeling, packaging, and advertising. Support new product development teams with regulatory strategy and submission pathways. Qualifications & Requirements Bachelors or Master’s degree in Engineering, Life Sciences, Pharmacy, or related field. Minimum 2 years’ experience in quality and/or regulatory roles in the medical device industry. Strong knowledge of ISO 13485, FDA 21 CFR Part 820, EU MDR/IVDR, and related standards/regulations. Experience preparing regulatory submissions (510(k), PMA, CE Mark, etc.). Lead Auditor certification for ISO 13485 (preferred). Excellent written and verbal communication skills. Strong organizational and project management abilities. Key Competencies Detail-oriented and analytical. Problem-solving and decision-making skills. Ability to work cross-functionally and lead teams. Up-to-date with global regulatory trends and requirements. Location: [Insert location] Employment Type: [Full-time/Part-time/Contract] Let me know if you want to add anything about company culture, reporting structure, or specific product lines!

Role & responsibilities Conduct Department Wise Audits to check whether they are working as per their SOP or not and to find the scope of improvements in their existing processes. (Sales, Pre Sales, Project-CD, Project-CR, Design-CD, Design-CR, Purchase, Quality, Production, Assembly, Packing-CD, Packing-CR, Store, Maintenance, HR, IT, HSE, Dispatch) Record and formalize the findings and submit the formal Audit Report to the respective Process Owner with a deadline and rating for improvement Keep a track of timely closure of these Audit ratings and closure evidences and send repeated reminders and status updates to the concerned person on every Monday. Escalate the non-submissions/delayed submissions report to the Management on every Saturday. Help the concerned person in updating their Processes/SOPs/Rules in standard PWSPL formats and get the new Process Document signed by impacted Internal Users and announce the same as an updated process to all impacted users. Write detailed Procedures and SOPs as per Company/Department gaps and circulate with concerned departments after their signoff to ensure their's no re-occurence of gap. Any additional travel to Project Sites to identify issues/non compliances and perform RCA and CAPA on the same. Keep centralized tracking of all company procedures, documents, with their latest revisions, revision history of changes, Audit reports, Audit Action Closure Tracker, etc in a systematic manner to be presented to management in weekly review meetings as & when required. Preferred candidate profile ISO 9001 Lean Manufacturing Quality tools Good Spoken and Written English Communication Documentation & Reporting Quick Learner Risk Identification and Mitigation Ability to match Organizations Quality Vision Self-Motivation MS Office Suite 5S Kaizen CAPA QMS Knowledge Adaptability Team Management Gap Analysis Continuous Improvement Time Management HSE Leadership Quality Standard Eye for Detail Knowledge of measuring tools Analytical & mathematical aptitude Interpersonal Coordination Decision making Pro activeness

Role & responsibilities: Daily planning with Fabrication team, monitoring of Fabrication as per Fabrication drawings, quality testing as per standard, daily reporting of fabrication progress, documentation etc... Preferred candidate profile: Candidates with only Diploma - Mechanical with 5 Years experience & ITI - Fitter with 10 Years experience are only eligible. The Candidate must be well versed with computer and must be fluent in English in both verbal & writing Skills. Age: Below 40 Years only ( Candidates above 40 Years are not eligible)

Hiring for QA Manager | Bahalgarh | Sonipat in Railway Industry Exp.- 8-11yrs Salary- 50-70k Candidate must have knowledge of Railway Industry and casting, steel melting Interested candidate contact on- 8222822052

Responsibilities: Ensure compliance with ISO standards through documentation management. Maintain confidentiality at all times. Manage documents using DMS software. Coordinate meetings and travel arrangements. Accidental insurance Performance bonus Leave encashment Gratuity Provident fund Maternity leaves Special parking for expecting mothers Prevention of sexual harrassment policy

Job Description: We are looking for a detail-oriented and proactive ISO 9001 Compliance Specialist to lead our efforts in achieving ISO 9001 certification. The ideal candidate will have extensive knowledge of ISO 9001 standards and experience in preparing manuals, developing processes, and ensuring overall compliance. Key Responsibilities: Develop and implement ISO 9001 compliant processes and procedures. Prepare and maintain the ISO 9001 Quality Manual. Conduct internal audits to ensure compliance with ISO 9001 standards. Provide training and support to staff on ISO 9001 requirements. Identify areas for improvement and implement corrective actions. Liaise with external auditors and certification bodies. Ensure continuous improvement of the Quality Management System (QMS). Qualifications: Bachelor's degree in Engineering, Quality Management, or a related field. Proven experience in ISO 9001 implementation and compliance. Strong understanding of ISO 9001 standards and requirements. Excellent organizational and project management skills. Ability to work independently and as part of a team. Strong communication and interpersonal skills. Certification in Quality Management or related field is a plus. What We Offer: Competitive salary and benefits package. Opportunity to work with a dynamic and innovative team. Professional development and growth opportunities. A supportive and collaborative work environment. How to Apply: Interested candidates are invited to submit their resume and cover letter detailing their experience and qualifications to WhatsApp +919820274179 or email: info@samaaaerospace.aero

"We are hiring for Manufacturing company." Position: Document Controller {Document Control Specialist 4_INR} Qualification: Bachelors degree in business administration, Information Management, Civil/Mechanical Engineering, or a related field. Experience: 6-8 Years Location: Ahmedabad Job Summary: We are looking for a highly organized and detail-oriented Document Controller to manage and maintain project documentation for large-scale projects. The ideal candidate will be responsible for controlling the flow of technical documents, drawings, submittals, correspondences, and records to ensure timely communication, secure storage, and strict adherence to document control protocols and industry standards. Key Responsibilities: Establish, maintain, and manage an effective document control system for all project documentation. Receive, log, review, track, and distribute incoming and outgoing documents such as drawings, technical submittals, RFIs, method statements, reports, and meeting minutes. Ensure documents are properly formatted, coded, indexed, and version-controlled in accordance with approved procedures. Coordinate with internal teams, contractors, consultants, and vendors for timely submission, review, and approval of documentation. Maintain up-to-date document registers and logs for traceability and audit purposes. Prepare transmittals, issue documentation, and manage acknowledgment workflows. Monitor document review cycles and alert responsible parties for pending or overdue actions. Handle sensitive and confidential documents with integrity and discretion. Perform routine audits to ensure consistency, completeness, and compliance with quality standards. Assist in compiling project closeout documentation, handover dossiers, and as-built records. Educational Qualifications: Bachelors degree in business administration, Information Management, Civil/Mechanical Engineering, or a related field. Certification in Document Control, Records Management, or EDMS (preferred). Required Experience : Minimum 6-10 years of experience in document control, specifically in Mega EPC Project is must. Technical Skills : Proficiency in Electronic Document Management Systems (EDMS) such as Autodesk Construction Cloud, SharePoint, or equivalent. Advanced knowledge of Microsoft Office Suite (Excel, Word, Outlook). Familiarity with construction documentation, technical drawings, and regulatory requirements. Understanding of ISO document control standards and QA/QC protocols. Experience with markup tools (e.g., Bluebeam, Adobe Acrobat Pro) is an added advantage Interested candidates can apply on What's App No.: 91 63574 05360 E-mail ID: twinkle.chauhan@aloissolutions.com

Role & responsibilities 1) Inspection & certifying of all incoming engineering material based on purchase specification. 2) Ensure of all preventive maintenance done as per schedule & check list. 3) Maintaining history of all equipment both stationary & rotating. 4) Effective utilization of contract labor with proper safety precautions. 5) Ensure no wastage of any engineering item & good housekeeping at work place. 6) Participate for Preparing appraisal for all fitters/electrician/instrument technician of engineering department. 7) Plan to complete breakdown in minimum time. 8) Prepare & maintain of all ISO related document record. 9) Develop new work procedures as required, in conjunction with relevant persons. 10) Provide personal protective equipment and clothing if hazards cannot fully be eliminated. 11) Identify and control hazardous conditions & wastes 12) Report section accidents and injuries to higher up. 13) Maintain compliance with all environment, health and safety policies and procedures by regular performance review. 14) Assist superiors in conducting regular inspections to identify risks/aspects, implement corrective action and arrange monitoring where required. 15) Take reasonable care for the safety & health of his / her own and that of other people who may be affected by their conduct in the workplace. 16) Ensure that any hazardous conditions, near misses and injuries are reported immediately to the superior 17) Under direction of Site main Controller undertake duties as required by agreed emergency procedures. 18) Needs & expectation of Top Management, Customer (Internal, External), Vendor &Staff. OH&S Related Execute the operational control of OHSAS/safety controls and their effectiveness study. Participate in the risk analysis in the initial stage & in case of any changes in material, machines, and method. Participate in the medical check-up camp and follow the doctor advice. Work permit issue & ensure its effective implementation. Participate in department safety committee meeting. Perform role related described in the emergency preparedness plan. Implement action arising out of plant safety audit & inspection. Timely completion of CAPA Role Challenges: To Ensure effective relationship with all external & Internal Stakeholders. To Ensure Effective change management to drive excellence at Mahad Privi Behavioral Competencies Managing Business Business Acumen Change Management Managing Others Building Team Nurture Talent Managing Self Innovation and Creativity Drive Results Functional Competencies 1. Tech skill related to utility operation 2. Knowledge of TPM 3. Problem solving skill 4. Compliances management

Role & responsibilities 1. Inspection & sampling of Raw materials / Packaging materials / Finished Goods as per sampling plan. 2. Analysis of Raw material / Packaging material / Intermediates / Semi processed materials & Finished Goods in complete manner as per the current specification 3. Carrying out regular test i.e. or analeptic & physico - chemical analysis of WIP and F.G. 4. Filling up the analytical protocols in a clear and legible writing, entering all Data in the Software. Systematically storing all the records and documents. 5. Maintaining reserve samples of RM systematically up to additional three months after receipt date. 6. Conducting calibrations checks of all Lab instruments regularly on its due intervals. 7. Reporting non-conformance immediately to Executive-QC / Production for further necessary action. 8. Conducting stability analysis under the guidance of QC/QA Manager. 9. Maintaining documents and data as per the requirement of -14001, ISO-9001 and ISO-18001 10. Reserve control samples of RM and FG with proper labeling 11. To train and guide lab assistant in collection of spills, containing, cleaning and neutralizing of spilled and or expired lab chemicals/ reagents before being disposal. 12. Use of appropriate PPE while carrying out sampling of hazardous chemicals 13. Maintaining spill kits at handy to contain any accidental spillages and aware of disposal procedures. 14. Perform other tasks as requested or assigned. 15. Help to achieving objectives, completing EMPs and SMPs. 16. Provides assistance during audits & inspection 17. Implements QMS & EMS requirements relevant to the work area 18. Ensure continual improvement of QMS and EMS and comply with defined procedures. 19. Under direction of Site main Controller undertake duties as required by agreed emergency procedures. 20. In case of unit 1 and 3 he can look after the dispatch activity of Finished goods as per SOP with coordination with QA department and report any abnormality to QA Privi Behavioral Competencies Managing Business Business Acumen Change Management Managing Others Building Team Nurture Talent Managing Self Innovation and Creativity Drive Results Functional Competencies 1. Chemistry 2. All Systems related to QC lab knowledge 3. Trouble shooting 4. Communication skill

Reports to: AGM Purchase Requirements: Education: B.E/B.Tech (Any Field)/ courses in material management Experience: Min 1 Years of relevant (Mechanical systems in Industrial/Power plant/Refinery) work experience with EPC firms Technical: Rudimentary technical awareness on raw material grades, mechanical, electrical and instrumentation equipment. Others: Good communication and negotiation skills. Ability to work under pressure and meet rigorous deadlines. Roles Responsibilities: Scrutinize and Review of indents to understand project requirements. Sending out RFQ to approved vendor as specified by the projects. Obtaining quotes and technical compliance form vendor and coordinating with the Engg/Project division to close indents. Releasing Purchaser orders to chosen vendors after due discussion with the department head management. Ensuring timely submission of necessary documents from chosen vendor to ensure timely approval of engg documents. Engaging in discussion with vendor and internally to resolve any issues during engineering approval. Communicating manufacturing clearance to vendor after a[approval of documents Engaging the vendor for periodic manufacturing status and timely dispatch of finished materials Organizing logistical support based on project team requirement. Sourcing new vendors for various items while maintaining vendor ties with regular vendors. Maintaining ISO documentation, Record Keeping, Suppliers/Manufacturers Data bank records.

Preparation of project justification and approval notes, regular review with department HOD. Project progress report preparation and review with next level Project wise budgeting and monitoring, be accountable for making annual CAPEX budget Be accountable for small scale equipment installation, ensure installation quality meets the technical use needs of manufacturing department. Be accountable for new equipment s selection, technical discussion with suppliers, installation management, equipment checking and acceptance to assure equipment quality. Regular communication with project cross functional team and share relevant information time to time. Be accountable for safety management of outside equipment supplier and their installation team to avoid safety accidents. Responsible for routine facility maintenance and minor repair of the basic factory infrastructure. Knowledge of Compliance, internal audit and ISO documentation for the plant Engineering Project area is also preferred. Generate ideas and suggestions on equipment improvement.

The ISO Quality control / Assurance is responsible for supporting the Quality Assurance Department with all ISO 9001 related quality assurance requirements for the ISO 9001 Quality Management System (QMS) Internal audit; External/Customer audit.... Required Candidate profile The ISO Quality will ensure the ISO 9001 QMS demonstrates its ability to consistently provide products &services that meet customer & statutory & regulatory Lead investigations of customer complaints

Any Graduate or DE / BE (Electrical/Mechanical) 5 - 7 Years Expertise in ISO standards,quality management systems,auditing procedures, documentation control,process improvement methodologies,leadership abilities, & effective communication skills.

We are looking for a Quality Control Engineer who will be responsible for ensuring the quality of stainless steel tanks, components, and stamped products meet the companys standards and customer expectations. The role involves hands-on inspection, defect analysis, process monitoring, and supporting continuous improvement initiatives. Key Responsibilities: Perform in-process, incoming, and final inspection of stainless steel tanks, stamped components, and assemblies. Use precision instruments such as vernier calipers, micrometers, height gauges , etc., to check dimensions and tolerances. Interpret engineering drawings and manufacturing tolerances (GD&T). Monitor welding quality (TIG/MIG), seam finish, leak testing, and overall product aesthetics. Conduct quality patrols on the shop floor to ensure adherence to SOPs and quality standards. Prepare and maintain quality documentation, inspection reports, rejection logs, and test records . Identify and report non-conformities (NCRs) and work with the production team to resolve quality issues. Support root cause analysis and corrective/preventive actions (CAPA) for recurring issues. Participate in internal audits, ISO documentation, and process control plans . Assist in training production staff on quality standards and visual inspection criteria. Key Skills Required Strong understanding of QA/QC procedures in manufacturing and 5S methodology . Proficient in measurement tools and inspection techniques Extensive knowledge of welding inspection and surface finish quality Familiarity with implementation of ISO 9001:2015 QMS Good knowledge of MS Excel, quality formats, ERP systems and reporting tools. Analytical thinking and problem-solving using 5 Why/Fishbone. Attention to detail and discipline in documentation.

Job Description: - Must have experience in the Injection Moulding Plant. Initiating, leading & proper planning of production settings, change overs and schedules. Trouble shooting & analysis of the injection moulding process defects. Knowledge of KAN - BAN. Knowledge of implementation & maintaining of 5 - 'S', ISO, IATF activities. Knowledge of generating shift wise daily production, rejection data & comparison analysis reports. Effective implementation and maintaining of predictive and preventive maintenance of machines. Education :- BE in Mechanical / Diploma in Mechanical Engineering Experience :- 5 years Plus Perks and Benefits :- Salary Rs. 4,20,000/- up to 4,80,000/- LPA Interested candidates can share CV to konarakhr123@gmail.com / 08970550662

S&V Industries is a USA-based company and pioneer in Global Supply Chain Management (SCM). For more details, refer to the company portal. This position is based out of Coimbatore, India. The selected candidate needs to travel throughout India as required. Travel to suppliers would likely be 20-40% of the time and will fluctuate based on project demands. There is no set schedule for travel, rather visit suppliers when there is an urgency to sit with them face-to-face Essential Duties and Responsibilities include the following. Other duties may be assigned. Create and maintain project schedules, including task assignments and timelines. Collaborate with cross-functional teams to develop project plans and objectives. Facilitate communication and collaboration among team members, including product managers, engineers, designers, and other stakeholders. Ensure that team members are aware of their responsibilities and deadlines. Assist in resource allocation and tracking, ensuring that the project has the necessary resources to meet its goals. Monitor and manage project budgets and expenses. Identify and assess project risks and develop mitigation strategies. Address issues and roadblocks as they arise to keep the project on track. Maintain accurate project documentation, including meeting minutes, status reports, and project plans. Provide regular updates to senior management and stakeholders on project progress. Ensure that project deliverables meet quality standards and adhere to product specifications. Conduct quality assurance checks and implement necessary improvements. Stay informed about industry regulations and standards relevant to product development. Ensure that products are developed in compliance with all applicable regulations. Identify opportunities for process improvement and best practices in new product development. Implement changes to enhance project efficiency and effectiveness. Manages on-time delivery and mitigates excess inventory. Facilitates customer onboarding and VMI agreements at the direction of the New Parts Development Manager. Follows all procedures in relation to the NPD process.

Urgent opening for Quality Manager.Candidate should have hand on experience on QMS / Testing methodologies.technical documentation. OHSAS, EMS. Audit based on ISO.

Key Responsibilities: 1. Quality Management System (QMS): Implement, maintain, and continuously improve ISO and GMP-based quality systems. Develop SOPs, inspection protocols, and checklists for each production stage. Ensure adherence to quality standards throughout the plant. 2. Process Quality Control: Monitor and manage quality parameters in blown film extrusion (gauge, width, clarity, tensile strength, etc.). Ensure sealing strength, print quality, and bag dimensions are within specification. Conduct real-time quality checks on shop floor and maintain traceability records. 3. Raw Material & Incoming Inspection: Establish incoming QC for raw materials such as biopolymers, masterbatch, ink, and packaging materials. Coordinate with procurement and suppliers for COA review, sampling, and approvals. 4. Customer Complaints & RCA: Lead investigations for customer complaints and internal quality issues. Perform root cause analysis (RCA) and implement corrective & preventive actions (CAPA). 5. Team Management & Training: Supervise the quality team across shifts. Train operators and line staff on quality standards and defect identification. 6. Documentation & Reporting: Maintain inspection reports, rejection logs, and production quality data. Present regular quality performance reports to senior management. Requirements: Education: B.Tech / Diploma in Plastics, Chemical Engineering, or related field. Experience: 610 years in quality control/assurance within blown film extrusion and packaging (preferably compostable or plastics industry). Hands-on experience in film quality testing (e.g., tensile, dart drop, sealing strength). Familiarity with ISO 9001, ISO 14001, and compostability certifications is a plus. Strong analytical skills, attention to detail, and shop-floor discipline.

Role & responsibilities Verify all saved and logged files for RFID tag orders, ensuring accuracy and completeness in record-keeping. Conduct periodic sampling and data checks on RFID tag production as part of routine quality inspections, identifying any discrepancies and ensuring compliance with quality standards. Perform thorough quality inspections on RFID products during production and post-production phases to verify compliance with specified performance and regulatory standards. Collaborate with cross-functional teams to address quality issues, participate in root cause analysis, and implement corrective actions. Document and maintain comprehensive quality records for traceability and auditing purposes, ensuring all records meet regulatory and internal standards. Develop, refine, and implement quality control processes for RFID tags, contributing to continuous improvement initiatives and standard operating procedures. Assist in training and guiding team members on quality standards and best practices for RFID tag manufacturing and handling. Support internal and external audits by providing quality records, data, and insights on the quality control processes and outcomes. Stay updated on industry trends, standards, and compliance requirements related to RFID tags and quality management. Familiarity with root cause analysis, corrective, and preventive actions (CAPA), and process improvement techniques. Product OI form & Assistance for software Before any tag/label production, verify the line set up and check few samples then give go ahead for production Ensure tag or label printing is checked before production Ensure adherance to ISO quality standards Preferred candidate profile Working in RFID Tags & Label manufacturing company.

Research and identify new business opportunities in the phytoextracts/herbal extract industry globally Design and execute technical marketing strategies for B2B export markets Establish and nurture strategic partnerships and key client relationships Participate in international/domestic exhibitions and audits Plan and oversee dispatches in coordination with packing, logistics, QA, and accounts Customize products based on client requirements and ensure alignment with production Ensure timely delivery, documentation, and post-dispatch client follow-ups Handle ISO/QMS documentation and represent the company during audits Preferred Candidate Profile Core experience in B2B Export Business Development in herbal/phytoextract industry Excellent communication, documentation, and technical sales skills Prior exposure to ISO audits, international expos , and client lifecycle management Educational background in M.Sc. (Biochemistry/Biotech) ; MBA (Marketing) is an added advantage Willing to work from Ahmedabad and travel for business needs