1381 Qms Jobs - Page 47

QMS, QA, QC, process quality, product quality, heavy engineering fabrication, NDT level inspection, ASME Section VIII, API, WPS, PQR, WPQ, RT, UT, PT, MT, and VT. Supplier quality, manufacturing, production, inspection inhouse and supplier. Required Candidate profile BE/BTech Mech with 15 to 20 years experience in heavy engineering fabrication, pressure vessel, tank, heat exchanger, boiler, QMS, QA, QC, quality audit, ready to work in Coimbatore.

Min 1 yr BPO Quality Manager Exp , AM/DM cannot apply Manage BPO Quality Team Call Callibration, Quality Audit, Quality Score , CSAT WFO- Bangalore only- APPLY ONLY IF CAN RELOCATE whatsapp CV Amit 8851792136, Neha 8287267407 Required Candidate profile WFO-Gurgaon/ Bangalore ,Apply those who can relocate No position in KOL/Pune IMMEDIATE JOINER GRADUATE whatsapp CV Amit 8851792136, Neha 8287267407

2 yr BPO Quality Manager on the paper(Insurance outbound sales)..Training Manager will be an advantage Exp , AM/DM cannot apply Call Callibration, Quality Audit, Quality Score , CSAT Required Candidate profile WFO-Kolkata only not for Delhi/NCR and Bangalore .Apply those who can relocate in Kolkata IMMEDIATE JOINER GRADUATE Call/whatsapp CV Amit 8851792136, Neha 8287267407

Qualification - B. Tech, Any Graduate Relevant Experience : 4 to 14 Years RESPONSIBILITIES: 1. To plan production activity based on production schedule. 2. To ensure that the raw materials and packing materials indents are received from QA and given to stores well in advance to meet the production schedule. 3. To ensure that the raw materials and packing materials are received in time from stores to avoid down time. 4. To co-ordinate with Engineering department and ensure that the preventive maintenance of all machineries are done on planned preventive maintenance day. 5. To co-ordinate with inspection section and get the trend of rejections and to initiate appropriate corrective actions. 6. To ensure discipline in the section, to practice cGMP at every stages of production. 7. To identify the training requirements of officers working in the section and to impart training to officers working in production section. 8. To ensure high yield and maximum productivity. 9. Conduct periodic internal review or audit to ensure the compliance. 7. Evaluating the efficiency of controls and improve the quality continuously. 8. Collaborate with cross functional team to monitor enforcement of standards and regulation. 9. Review the work of down level employees when necessary to identify compliance issues and provide the training. 10. Keep abreast of regulatory developments within the department as well as evolving best practices in compliance control. 11. Daily GEMBA within the department to ensure the compliance. 12. To run the department in a cost effective manner. 13. Co-ordination with other departments. 14. To train the employees and officers on aseptic culture and the importance of following aseptic culture in a pharmaceutical manufacturing unit producing injectable. 15. To ensure that the stationery/consumables required for the plant is indented/made available in time. 16. To raise deviation/incident and change controls, as applicable. 17. To ensure proper housekeeping in the department. 18. To ensure that the operators and officers are strictly following systems and SOPs at every stage. 19. To put proposals for continuous improvement of the plant operations. 20. To ensure that the equipment and machineries used in the plant are validated/revalidated in time by proper co-ordination with Engineering and QA departments. 21. To co-ordinate and execute the validation for new equipment. 22. To ensure that all technical aspects and qualitative measures are strictly followed/ensured in every batch production. 23. To monitor aseptic process simulation study and batch activities at all the stages. 24. To ensure documentation and control on documents. 25. To make recommendation for automation of the unit/activity. 26. To practice Quality Management System at every stage of the work. 27. To report to Production - Manager. Thanks & Regards Praveen Kumar M ****************************** E-mail : praveenkumar@bvrpc.com

Role & responsibilities Cross functional and within department co-ordination to ensure all the Change controls, Exceptions, Process non-conformance and Material non-conformance for the closure within due date. Responsible for all the change control coordination activities, Coordination with customers for approval of change controls in Quality management system module Monitor and to trace the Change controls, Exceptions, Process non-conformance and Material non-conformance in Quality management system Initiate, review the Corrective action & preventive action and to coordinate with other departments for its closure within due date. Prepare and review the trends for Change controls, Process non-conformance and Material non-conformance, Exceptions and Corrective action & preventive actions Preferred candidate profile 02 to 07 years pharma formulations experience preferrable. Perks and benefits As per Industrial standards

To release audit plan to the client site under audit by adhering to the EHS / ISO 9001 rules and the TUV SUD internal guidelines. To plan effectively and efficiently in time the travel plan for himself and the audit team where the audit planned as Lead auditor for the audit to achieve cost effective audit. To release the audit documents (Final audit plan, audit report and NCs) to the client site under audit by adhering as per rules and the TUV SUD internal guidelines. To close the audit file by arranging the action plan against the issued NCRs after audit from the client in an effective and time bound manner as per EHS / ISO 9001 rules and the TUV SUD internal guidelines. To support Branch in attending the goals and targets set by providing efforts towards the same

Good verbal&written English communication skills Good Interpersonal Skills Email etiquettes &Telephone etiquettes Good Team Player & Team management skills Project Management Skills Excellent MS Office skills Risk identification assessment mitigation Required Candidate profile 12PM to 9PM (Flexible to work between 11AM to11PM) certification:ISO27001,ISO9001,PCI-DSS,SOC2,HIPAA,Conduct periodic &ad-hoc internal audits for scoped businesses Queries:8652547205/anisha@peshr.com

Optimus Generics Ltd. is looking for Quality Assurance to join our dynamic team and embark on a rewarding career journey Developing and executing test plans and test cases for software products and applicationsIdentifying, analyzing, and documenting defects and issues found during testingCollaborating with developers to resolve issues and ensure that software meets customer requirementsDeveloping and implementing automated testing frameworks and toolsConducting performance and load testing to evaluate software performance and stability Developing and implementing best practices for testing and quality assuranceCommunicating with stakeholders and team members to report on testing progress and resultsParticipating in the design and development of new software products and applicationsConducting usability testing and providing feedback on user interface design and functionalityParticipating in continuous improvement activities and implementing process improvements to improve testing efficiency and effectiveness Solid understanding of software quality assurance and testing methodologies Strong analytical and problem-solving skills, as well as excellent communication and teamwork skills

About Raptee Energy Raptee Energy is a full- stack electric motorcycle startup with a very strong technical moat, founded in 2019 by four engineers from Chennai (Ex Tesla, Wipro), working on bringing a no-compromise upgrade motorcycle to an otherwise scooter- only EV market. Raptee is incubated at CIIC ARAI. Job Summary At Raptee, we are seeking a passionate Supplier Quality Engineer who will ensure that all products delivered by suppliers are in compliance with manufacturing specifications, Raptees standards, and industry norms. Responsibilities Ensure the Parts are approved thro PPAP system before mass production ( Both NPD, ECN and Capacity Enhancement projects ) for 2 Wheeler Mechanical parts Establish systems and processes for eliminating early failures of supplier parts in new products and regular products and maintain consistency Support Assembly line to achieve Vehicle Straight Pass Ratio by eliminating the defects in supplier parts Ensure the Lot Rejection, Samples Rejection and Line Rejection, Customer Rejection targets are met as per the policy targets Ensure effective APQP systems are deployment in Supplier works for any new development ( DFM Studies, FMEA, CP, Cpk Study, Tier 2 selection, FTG implementation, PSW ) Review progress of achievement of process capability of target quality parameters consistently in manufacturing of supplier parts ( Cpk improvement projects ) Analyze and implement corrective actions on Supplier products and process and ensure the implemented actions are sustained at supplier works Review and control maintenance of all standards pertaining to supplier parts manufacturing Conduct Process and System audit at supplier works and ensure the supplier quality Management Systems are sustained and assure Zero Defect supplies consistently Effectively implement Product / Process changes to meet Raptees design requirements with valid PPAP approval Communicate to Plant and Suppliers on Product changes and ensure latest QMS documents are available with Supplier Establish the Agreement of Inspection, Receipt Inspection Standard, Supplier PDIR before SOP for NPD and ECN Changes Ensure 100% FTG ( Fixture, Tools and gauges ) availability prior to mass production and validated thoroughly as part of PPAP approval Ensure 100% compliance to IATF 16949 QMS System on daily management activities Benefits : Opportunity to work in a fast-paced and dynamic environment. Opportunities for professional advancement as the company undergoes expansion. A culture that fosters collaboration and creativity within the team. Collaborate closely with seasoned experts in the field. Gaining an entry point into the field of automobile development.

Develop and maintain systems, rules, and processes to ensure fulfillment of internal and external requirements. Ensures that projects and products are capable and will meet specified standards (Preventive). In-depth understanding of key business drivers; uses this understanding to accomplish own work. In-depth understanding of how work of own team integrates with other teams and contributes to the area. Job Description Roles and Responsibilities GEHC ONLY Creates a Quality culture by driving compliance activities around a specific product, site or region. This includes being responsible for the total quality management system for the business and driving Quality metrics. Ensures quality and regulatory compliance while driving process effectiveness and efficiency. Represents GE Healthcare to external agencies and champions the evolution of the quality culture which includes executing and driving quality objectives, metrics, reporting and operating mechanisms. Developing in-depth knowledge of a discipline. Uses prior experience and acquired expertise to execute functional policy/strategy. A job at this level is likely to be an individual contributor, with proven interpersonal skills. Communication with direct colleagues and the business about design and coordination services rendered. Provides informal guidance to new team members. Explains complex information to others in straightforward situations. Impacts projects, processes and procedures in own field. The role operates with some autonomy, but is focused on execution of activities/provision of advice within an enabling discipline covered by standard functional practices and procedures. Activities require professional judgment, but may require more senior levels of guidance. Utilizes technical expertise and judgement to solve problems. Leverages technical skills and analytic thinking required to solve problems. May use multiple internal sources outside of own team to arrive at decisions. Possesses knowledge on QMS parameters with respect to ISO 13485 standards, including but not limited to, prior experience in handling Non-conformances, CAPA, Concessions and Deviations. In-depth and hands-on knowledge on process risk assessment and risk management with respect to ISO 14971 will be a key responsibility. Understands the process principles and drives the establishing, monitoring, and maintenance of all key performance indicators for product and process quality, with the support of cross functional teams for ongoing projects and new projects Demonstrate knowledge on Medical devices Refurbishment, Repairs and Harvesting. Required Qualifications For roles outside of the USA- This role requires advanced experience in the Quality Healthcare Quality. Knowledge level is comparable to a Bachelors degree from an accredited university or college ( or a high school diploma with relevant experience). For roles in USA - Bachelors degree from an accredited university or college (or a high school diploma / GED with at least 6 years of experience in Job Family Group(s)/Function(s)). Knowledge of standard and Regulations like ISO 13485, ISO 14971. Experienced with both Internal and External Audits in both Auditor and Auditee roles. Desired Characteristics Strong oral and written communication skills. Demonstrated ability to analyze and resolve problems. Ability to document, plan, market, and execute programs. Established project management skills.

Job Description Job Location: Kochi, Bangalore/Chennai/Hyderabad Job Scope and Accountabilities: To conduct audits/ Trainings as per the requirements stated in audit criteria To remain updates on all skill development, code qualification, Regulatory and Industrial requirements related to audits and certifications. To be competent and qualified in Various standards like BRCGS food, packaging, FSSC, ISO 22000, GMP etc. Upgrade the knowledge of local social, economic, and business environment. To ensure TAT- Turnaround time for audit reports as per procedures established by Eurofins. Supervisory Responsibilities: Mentoring Support of Technical executives, Auditors / Back office executives. Monitoring and support to Operational activities. Duties: To understand the role of impartiality when providing certification activities and the process of taking independent action where necessary, (e.g. informing authorities, accreditation bodies, stakeholders) To demonstrate the management expertise and ability to lead and take decisions. Review the decisions taken by technical manager relating to certification/verification. To demonstrate the ability to communicate with all stakeholders (e.g. Impartiality Committee, Directors) To ensure timely updating of qualifications and competency, satisfactory completion of training, calibration meetings, training audits, witness audits and approvals. Qualifications Bachelor s degree in appropriate discipline Preferably Food Science Lead auditor course FSMS/ FSSC /QMS or equivalent Minimum 5 year of experience in Operations, technical, Audits, prefera

Qualification: Regular M.Sc. (1st class is mandatory) - 60% Throughout in All Streams Work Experience: 6– 12 Years (In the field of QA in Pharma/Chemicals/Agrochemicals)

Role & responsibilities Develop and implement quality control procedures and guidelines. Monitor production processes to ensure compliance with quality standards. Conduct regular inspections and tests of raw materials, in-process components, and finished products. Identify and address any quality issues, deviations, or non-conformities. Document and maintain accurate records of quality inspection results and corrective actions taken. Collaborate with production teams to develop and improve quality control processes. Analyze quality data and generate reports to track trends and identify areas for improvement. Train and educate employees on quality control procedures and standards. Work closely with suppliers and vendors to address quality-related concerns. Stay updated on industry regulations and best practices in quality control. 8D model, exposure of Audits (Internal, External, Process), RCA, CAPA, 6S. Inspections. Understanding of UTM machine. . Preferred candidate profile Bachelor's degree in a relevant field, such as Quality Management or Textile Engineering. Proven experience in a quality assurance or quality control role. Strong knowledge of quality control principles and practices. Attention to detail and ability to work with precision. Proficiency in using quality control tools and software. Knowledge of relevant quality management systems and standards. Ability to collaborate effectively with cross-functional teams. Certifications in quality management (e.g., Six Sigma, ISO) are a plus. Good in excel and powerpoint.

SUMMARY Associate - Manufacturing (CNC Milling & Inspection) Ahmedabad, INDIA Position Code: 1207CA About the Role: We are looking for an Associate - Manufacturing (CNC Milling & Inspection), who thrives in a high performance and fast paced technical environment. As an Associate within the Manufacturing (CNC Milling & Inspection) team, you will be responsible for independently performing most function tasks, ensuring that our customer receives a great product. What you'll deliver: Work to team plan & deliver your tasks on-time & within budget Evaluate your work progress to the plan and make required course corrections Inward inspection of incoming material for cnc milling Pre - milling & setting of work-holding as per milling strategy defined in process documentation Accurately build cutting tools as per tool list and set the job on machine as per process documentation Understand milling strategy and ensure safe and efficient operation of 3-5 Axis CNC machines Understand part's form, fit and function in assembly and it's function Ensure that required aesthetic and dimensional accuracy is achieved during milling process Deburr, clean and inspect machined part to validate that all required characteristics are fully achieved Optimise milling efficiency with regular machine maintenance & Cutting Tool Krib organisation Duly complete operation, inspection and quality systems documentation Work with Design, APQP and Assembly team to ensure that customer requirements are met Swiftly resolve non-conformance to minimise impact on project objectives Deliver your work 'right first time' & 'on time in full' Understand project goals and objectives and complete your task within budget Follow processes, standard operating procedure (SOP) and apply best practices in your work Follow function's performance and improvement processes in your work Apply lean & 5S visual work environment principles in your work Align your work to meet your KPIs to achieve your growth goals Evaluate your KPI trend and implement required course corrections Utilise learning material & proactively participate in discussion forums Make your learning program to enhance your skills & knowledge Make & implement your performance & economic growth plan What you'll need: Passion for our Vision: Transform Manufacturing 2+ years of total working experience in related domain In - depth domain knowledge gained at an education institution or self - learnt Proficient knowledge of 3-5 Axis milling and cutting strategies of highly complex metallic components Proficient knowledge of full manufacturing cycle of large and complex assembly at very high-quality level Proficient knowledge of one off/low volume milling best practices & manual G & M code programming Proficient knowledge of 3-5 Axis machine operations using Siemens and Fanuc machine control systems Proficient knowledge of GD&T, fits and tolerances, aerospace materials, special processes & treatments Proficient understanding of quality management systems and ISO9001/AS9100 standards Proficient understanding of lean & six sigma principles Proficiency in engineering fundamentals and emerging technologies Proficient ability to identify risks, manage them and implement mitigating actions Flexibility to go beyond normal work hours in time of need and support other functions Must have: Attitude to positively work with cross functional teams Respectful behaviour and willingness to adapt company code of conduct Attitude to learn, do your best work and grow Initiative and courage to explore new ideas and learn from the mistakes Perfectionist approach and meticulous to the finest detail in everything that you do Clear and concise written & verbal English language communication as well as presentation skills Proficiency in Excel, Outlook, PowerPoint, Teams and other MS Office software Readiness work in different shifts to support customers in different time zone Nice to have: Proficient knowledge of CNC Machine maintenance & calibration Proficient knowledge of conventional machines like drilling, milling, lathe, surface, and cylindrical grinders Proficient knowledge of IOT application in milling operation Proficient knowledge of on-machine probing cycles and programming Experience of working with leading ERP software like - Epicor / SAP / NetSuite Great sense of humour

About The Role : Participate in daily review meetings with the Section Incharge to understand the daily production targets, inhouse rejection (IHR) targets, maintenance schedules and discuss variances (if any) in prodution Analyze production for the previous day (and/or shift). Compare against target to identify deviations and help plan for next steps to enable recovery of losses in the day / shift Create a work plan for production activities (during the day/shift) basis the daily section production requirement Oversee end to end production process including all cell operation routines aimed at achieving the production target Maximize plant production efficiency by monitoring and controlling production bottleneck areas Resolve various issues impacting production capacity of plant; Escalate to Section Incharge for critical issues Collaborate with maintenance teams as and when required to assess various maintenance requests basis risks involved to production. Aim at limiting machine breakdown to 3-4% and minimizing downtime Monitor actual production vs scheduled production; Understand the causes for the deviation and implement corrective actions to prevent future occurrences Provide daily updates regarding production activities, actual production, IHR, consumables utilization etc Monitor consumables per unit of product hence estimate the cost of manufacturing. Ensure consumption in-line with the consumables plan by optimizing utilization of the consumables Study and analyze previous day rejections to identify processes getting rejected and its subsequent causes and effects. Submit the IHR report to the Section Incharge for further analysis and planning Implement process modifications suggested by supervisor to control IHR thereby avoiding wastage of both quantity and cost Contribute to the implementation of Kaizen and initiatives suggested by ME ensuring plant is operated in compliance with best engineering practices Contribute to the review of plant operating procedures by provide inputs to modify the same to improve quality and performance of system Ensure all documents such as QMS requirements, log books, log sheets and safety documents are properly stored and maintained for future reference Ensure timely reporting and investigation for any HSSE related incident; Ensure effective and timely implementation of formulated action plan to prevent its reoccurrence Conduct timely trainings and talks for all production personnel and contract workforce on all HSSE, legal, environmental and fire compliances and management Facilitate internal / external audits and ensure compliance of all production processes to applicable environmental, health and safety policies, laws and regulations. Job Requirement BE / Diploma - Mechanical / Plastics / CIPET The person should have min. 5 + years of experience. The person should have worked in Polymer Auto-components.

About The Role : Experience in core Assembly line management Analyze production for the previous day (and/or shift). Compare against target to identify deviations and help plan for next steps to enable recovery of losses in the day / shift Participate in daily review meetings with the Section Incharge to understand the daily production targets, inhouse rejection (IHR) targets, maintenance schedules and discuss variances (if any) in prodution Create a work plan for production activities (during the day/shift) basis the daily section production requirement Oversee end to end production process including all cell operation routines aimed at achieving the production target Maximize plant production efficiency by monitoring and controlling production bottleneck areas Resolve various issues impacting production capacity of plant; Escalate to Section Incharge for critical issues Collaborate with maintenance teams as and when required to assess various maintenance requests basis risks involved to production. Aim at limiting machine breakdown to 3-4% and minimizing downtime Monitor actual production vs scheduled production; Understand the causes for the deviation and implement corrective actions to prevent future occurrences Provide daily updates regarding production activities, actual production, IHR, consumables utilization etc Monitor consumables per unit of product hence estimate the cost of manufacturing. Ensure consumption in-line with the consumables plan by optimizing utilization of the consumables Study and analyze previous day rejections to identify processes getting rejected and its subsequent causes and effects. Submit the IHR report to the Section Incharge for further analysis and planning Implement process modifications suggested by supervisor to control IHR thereby avoiding wastage of both quantity and cost Contribute to the implementation of Kaizen and initiatives suggested by ME ensuring plant is operated in compliance with best engineering practices Contribute to the review of plant operating procedures by provide inputs to modify the same to improve quality and performance of system Ensure all documents such as QMS requirements, log books, log sheets and safety documents are properly stored and maintained for future reference Ensure timely reporting and investigation for any HSSE related incident; Ensure effective and timely implementation of formulated action plan to prevent its reoccurrence Conduct timely trainings and talks for all production personnel and contract workforce on all HSSE, legal, environmental and fire compliances and management Facilitate internal / external audits and ensure compliance of all production processes to applicable environmental, health and safety policies, laws and regulations.

About The Role : Ensure the adherence of Supplier Quality and In-coming Quality Maintain Incoming parts quality, supplier monitoring and supplier audit Be Part of CFT to have concrete AOI development with CD team during development. Evaluate supplier product quality on regular basis and guide them to achieve consistency in quality. Participate in supplier CAT Meeting. Preparing and implementing supplier wise annual audit plan to improvement and evaluate the suppliers Analyzing the audit report and action plan from supplier for closing NCs Issue Supplier notification for quality issue, debit etc. Adherence of quality systems at In-process Quality Conduct the Internal audit of product & Manufacturing Processes and taking necessary corrective & preventive actions to prevent occurrences. Review Layout testing and Functional testing for production process. Enforce First off, last off, In-process product audit, control charts are implemented. To ensure the Identification and traceability of parts during process and supplies to customer. Maintain the QMS at Plant Provide the details of Customer QMS requirements to Employees Planning internal audit, coordinate to conduct management review meeting (MRM) & prepare minutes of meeting for necessary actions. Carryout IATF internal audit as per plan in coordination with BU QMS lead. Maintain QMS documents legibility & availability. Implement Inspection standard and work instructions related to all QA process Timely submission of revalidated reports and maintain layout inspection records etc. Preparing the plan for process, product and poka-yoke Audit and analyzing audit report. Preparing observation NCs report & tracking and verifying the actions against the NCs to ensure timely closure. Achieve Zero defect out-flow to Customer Control of master sample & revalidation. Promote awareness of customer requirements throughout the organization. Participate in APQP process. Establish Quality control measures at the identified critical control parameters. Ensure enough lighting is there in applicable parts checking area. Control on outsourced processes. Provide and check use of required PPEs to Shift Inspectors. Set the competitive targets for Inspectors to improve Quality and productivity Up-keeping available facility at Quality Lab Monitor the calibration of measuring instruments as per plan Controlling of measuring and testing equipment To follow on testing with outside lab & maintaining the QA lab. NPD Quality Review control plans (Pre-launch and full production) and identify product design and process concerns during product planning stage. Cross verify the documents (Setup approval/first piece approval/in process inspection/ final inspection/ dock audit) Develop action plan to reduce vital RPNs through ME team (Above set baseline) Be active member in CFT for development of Process documents during the Product Planning process (Gate 0) and all steps of DFMEA Participate as CFT member to Calculate the SOD (Severity x Occurrence x Detection) number or risk priority number (RPN) as part of PFMEA Communicate the importance of the implementation of QMS procedures to NPD (Program Management) and ensure alignment to VQS Ensure the entire new product development process has quality assurance built in every step Maintain the Customer Quality, Customer Complaint handling & IHR Attending customer complaint & analyzing defect/abnormality as per customer feedback & keeping documentation of corrective measures. Taking contentment action at customer end, warehouse & BSR. Doing root cause analysis & preparing action plan for taking corrective measures & horizontal deployments. Updating the corrective measures in FMEA Reporting to customer on process side & inspection side corrective action Improve PPM at customer ends. Participate in CAT meeting and reporting the action taken in timely manner to management and customers. Attending planed /surprise customer audit. Maintaining shop floor activities as per Customer Audit Check sheet in order to maintain customer audit score, product and process quality as per customers standard requirement (CSR). Preparing and implementing actions as per audit report observation and ensure timely NC closure. Maintaining warranty/EFR signoff documents and analyzing the same on timely intervention Maintaining Inspection agreement/ CSR and educating team on the same Monitoring inspection activity as per inspection agreement at final inspection along with Customer Specific Requirement. Monitoring SPC (Statistical Process Control) Monitoring & Improving process capability for product characteristic by using SPC toll to reduce variations. Conducting SPC study of process, setting control limits & training operators to use the same Employee Training & Development Conducting training as per the IATF & QMS requirement. Documenting employee skill & responsibility matrix and training employees for skill improvement. Awareness training to QA Engineers on SPC, MSA & PPAP. Ensure Employee involvement through Kaizen competition by involvement of all QA employees. Job Requirement Work Experience Minimum 10-12 years of experience Industry Related experience:Auto Component Manufacturing Skills and competency: Applicable QMS Standard Good Knowledge of SPC, FMEA, PPAP, 7QC Knowledge of Process and product knowledge Basic SAP 3G (Gemba, Gembutsu, Genjitsu) Control Plan & Inspection Process (Material, In-process & Product) Quality Control Process Documentation & Report Preparation MS Office Analytical Skills Strong Time Management and Priority Management Interpersonal Skill, Problem Solving, Teamwork

2 yr BPO Quality Manager on the paper(Insurance outbound sales)..Training Manager will be an advantage Exp , AM/DM cannot apply Call Callibration, Quality Audit, Quality Score , CSAT Required Candidate profile WFO-Kolkata only not for Delhi/NCR and Bangalore .Apply those who can relocate in Kolkata IMMEDIATE JOINER GRADUATE Call/whatsapp CV Amit 8851792136, Neha 8287267407

Roles Responsibilities: Carrying out inspection of machined components from sub contract at incoming / inward stage and ensure the drawing dimension and providing a Usage Decision in the SAP system. Verify the inspection reports of machined components from sub contract and compare with component drawing and ensure the quality requirements. Co ordinating with suppliers for getting right components and educating process and inspection methods. Co ordinating with cross functional departments like SCM / Purchase, Stores, Production, TOP department in order to clear the items. Arrange PMI test for the received components and ensure the PMI result with standards and clear it for next process. Providing the inspection support work for Machine shop 1 2 Attend the assembly issues related to sub-contract machined components. Allocate the TPI to sub supplier end for daily inspection based on buyer inspection request. Item code Approval for approved supplier in SAP system based on the request from concern buyers. Raise X2 Notification for the deviations observed during machined component inspection and assign to concern buyer and ensure the rework activity and closure of notification after getting feedback. Prepare the dimension report for API related components. Qualification and Experience DME with 5 - 7 years and BE (Mechanical) with 3 - 5 years of experience in relevant Valve Industry. Functional Skills Product Knowledge Knowledge in QMS Inspection Knowledge on machined components Qualification in NDT- PT Knowledge in Visual Inspection Behavioural Skills Communication Skills Team work

-We are looking out candidates for different sections and positions in Quality Assurance department. Such as IPQA, QMS, Lab QA, AMV QA. Interested candidates can share their resumes on a.salunkhe@v-ensure.com & n32admin@v-ensure.com Role & responsibilities 1) IPQA - In process Checks. - Line clearance - Review of BMR, BPR 2) QMS - Handling and review of Change control, deviations, CAPA of different departments. - Document issuance, archival, retrieval. - Facing the Audits. 3) Lab QA & AMV QA - Managing Analytical QA activities. - Review of documents related to QC i.e. Raw material, finished products, stability. - Review of documents of Method validation, Assay. Preferred candidate profile - Candidates must have experience in Pharma formulation plant. - Must have good communication skills. - Candidates from Regulatory plant will be given preference. - Immediate joiners will be preferred. Perks and benefits Best in the industry

• Ensure compliance with Stage Gate and Design QA procedures. • Coordination between different stake holders – R&D, QC, QA, RA, Project Management for effective Stage Gate reviews and clearances of Stages. • Review PDRs, Scale up reports including Lab Note books • Participate in designing DOE trials in line with Process • Review Scale up protocols, Exhibit protocols, Process Validation protocols and reports • R&D IPQA • R&D procedural compliances – Qualifications, Calibrations, RLD Management, Stability Management • Responsible for deviation, investigation related to R&D. • Responsible for specification/STP review. Review and clearance of Analytical Method Validations • R&D Documentation Management -Issuance and retrieval • Responsible for clearing Formulation Projects for Scale up and Exhibit batches.

SUMMARY Associate - Assembly (Jigs, Fixtures & Tooling) Ahmedabad, INDIA Position Code: 1208XA About the Role: We are looking for an Associate - Assembly (Jigs, Fixtures & Tooling), who thrives in a high performance and fast paced technical environment. As an Associate within the Assembly (Jigs, Fixtures & Tooling) team, you will be responsible for independently performing most function tasks, ensuring that our customer receives a great product. What you'll deliver: Work to team plan & deliver your tasks on-time & within budget Evaluate your work progress to the plan and make required course corrections Assembly of complex high precision jigs, fixtures and tooling at highest quality level Work with highest craftmanship level to achieve perfection in finest details of product In process inspection of dimensional accuracy and stage wise functional testing Make very fine adjustments to part dimensions to achieve optimum product function Excellent aesthetic appearance along with the functional requirements Optimise and fine tune product operation for ease of use at customer end Detailed and illustrative assembly and test documentation Work with design and manufacturing function to ensure that design objectives are realised Swiftly resolve non-conformance to minimise impact on project objectives Deliver your work 'right first time' & 'on time in full' Understand project goals and objectives and complete your task within budget Follow processes, standard operating procedure (SOP) and apply best practices in your work Follow function's performance and improvement processes in your work Apply lean & 5S visual work environment principles in your work Align your work to meet your KPIs to achieve your growth goals Evaluate your KPI trend and implement required course corrections Utilise learning material & proactively participate in discussion forums Make your learning program to enhance your skills & knowledge Make & implement your performance & economic growth plan What you'll need: Passion for our Vision: Transform Manufacturing 2+ years of total working experience in related domain In - depth domain knowledge gained at an education institution or self - learnt Proficient knowledge of large and complex assembly at very high-quality level Proficient knowledge of integrating mechanical, hydraulics, pneumatic, sensor, and automation Proficient knowledge of product and proof load testing Proficient knowledge of Solid works, Model Based Definition and drawing interpretation Knowledge of GD&T, fits and tolerances, aerospace materials, manufacturing processes & treatments Proficient understanding of quality management systems and ISO9001/AS9100 standards Proficient understanding of lean & six sigma principles Proficiency in engineering fundamentals and emerging technologies Proficient ability to identify risks, manage them and implement mitigating actions Flexibility to go beyond normal work hours in time of need and support other functions Must have: Attitude to positively work with cross functional teams Respectful behaviour and willingness to adapt company code of conduct Attitude to learn, do your best work and grow Initiative and courage to explore new ideas and learn from the mistakes Perfectionist approach and meticulous to the finest detail in everything that you do Clear and concise written & verbal English language communication as well as presentation skills Proficiency in Excel, Outlook, PowerPoint, Teams and other MS Office software Readiness work in different shifts to support customers in different time zone Nice to have: Proficient knowledge of electronics and sensor technology Proficient knowledge of electrical and wiring harness assembly Experience of working with leading ERP software like - Epicor / SAP / NetSuite Great sense of humour

SUMMARY Associate - Business Systems Ahmedabad, INDIA I Position Code: 1201XA About the Role: We are looking for an Associate - Business Systems, who thrives in a high performance and fast paced technical environment. As an Associate within the Business Systems team, you will be responsible for independently performing most function tasks, ensuring that our customer receives a great product. What you'll deliver: Work to team plan & deliver your tasks on-time & within budget Evaluate your work progress to the plan and make required course corrections Develop & Implement 'real-time audit ready QMS' as per AS9100, Nadcap and customer specific standards Effective implementation of lean manufacturing, Six Sigma and Health & Safety standards Optimised document and record generation to make QMS "Fun to Use" for the team Successful internal audit, external audit, supplier audit reports and health & Safety records Performance evaluation and improvement process development and implementation Swiftly resolve non-conformance to minimise impact on project objectives Deliver your work 'right first time' & 'on time in full' Understand project goals and objectives and complete your task within budget Follow processes, standard operating procedure (SOP) and apply best practices in your work Follow function's performance and improvement processes in your work Apply lean & 5S visual work environment principles in your work Align your work to meet your KPIs to achieve your growth goals Evaluate your KPI trend and implement required course corrections Utilise learning material & proactively participate in discussion forums Make your learning program to enhance your skills & knowledge & competency Make & implement your performance & economic growth plan What you'll need: Passion for our Vision: Transform Manufacturing 2+ years of total working experience in related domain In-depth domain knowledge & competency gained at an education institution or self-learnt Proficiency Knowledge & Competency of QMS based on ISO9001/AS9100 & Nadcap standard Proficiency Knowledge & Competency of lean & six sigma principles Proficiency Knowledge & Competency of paperless system using ERP & other latest software platforms Proficiency Knowledge & Competency of organisation level risks management and mitigation Proficiency Knowledge & Competency of intuitive & user friendly quality management system Proficient understanding & competency of quality management systems and ISO9001/AS9100 standards Proficient understanding & competency of lean & six sigma principles Proficiency in engineering fundamentals and emerging technologies Proficient ability to identify risks, manage them and implement mitigating actions Flexibility to go beyond normal work hours in time of need and support other functions Must have: Attitude to positively work with cross functional teams Respectful behaviour and willingness to adapt company code of conduct Attitude to learn, do your best work and grow Initiative and courage to explore new ideas and learn from the mistakes Perfectionist approach and meticulous to the finest detail in everything that you do Clear and concise written & verbal English language communication as well as presentation skills Prompt and on-time communication of operational matters Proficiency in Excel, Outlook, PowerPoint, Teams and other MS Office software Readiness work in different shifts to support customers in different time zone Nice to have: AS9100 Internal & External audit experience Supplier audit experience Experience of working with leading ERP software like - Epicor / SAP / NetSuite Great sense of humour

Greetings from Xelentra!! One of Our Top Home Textile Manufacturing Company in Karur is On the Look Out For: Quality Manager Technical Compliance - Textiles Reporting to Managing Partner Number of Vacancies: 1 Location: Karur Qualification: Any Graduate (Preferably from Textile background) Must Have A Complete Knowledge in QMS Age: Around 35 – 40 years Experience: - 7-10 Years Package: 9 – 14 Lacs Job Description: QMS – Technical Compliance: QMS & Technical Audits Coordinating Will all Departments to Comply with QMS Requirements. Preparation of ISO MR Documents Like AOD, Internal Audits, MRM & Risk Assessments. Coordination with Certificate Bodies for Technical Audits (QMS, GOTS, OCS, GRS, OEKO-TEX & Client COC Audits) & Follow up For NC Closures. GOTS, OCS, GRS &RCS Certification Yearly Renewal and Its Audits Follow ups. Coordinating With All Departments Related to GOTS, OCS, GRS & RCS Requirements Collection of Raw Materials TC’s from suppliers and Preparation of TC’s For Shipments BCI BCI Membership Yearly Renewal and Its Audits Follow Ups. Coordinating With Purchase Team For Sourcing BCI Raw materials and Its BCP TR’s & BCCU Credits From Suppliers. Maintain BCI Records and Issuance of BCP TR’s To Customers. OEKO – TEX Certification Renewal & Its Sourcing Suppliers Certificates and Its Renewal Documents Preparation & Follow Up Every Year. STEP: Certification Requirements & Records Maintenance Follow Ups. CE & UKCA : Certification and Its Testing Requirements Follow Up Depending on Customers Requirements & its Renewal Follow Ups. WORLDLY ( HIGG INDEX – Including EMS, CMS & WMS ) – Requirements Follow Ups DETOX – Test report Follow Ups with Our Wet Processing Units. Interested and Relevant Talents Send Your Updated CV in Word Format to My Mail Id hr@xelentra.in and Contact Akilabalan 98940 - 40086. It is an Urgent Opening! Rush Your CV’s! Looking For Immediate Joiners Regards Akilabalan | Xelentra

• Responsible for Defining and Implementation of Quality Management system and Quality Assurance processes across OSD and CMO/ CRO locations. • Ensuring compliance with all cGMP requirements in line with global and Indian regulatory requirements • Handling all Regulatory audits, Client Audits, Internal Audits • Responsible for Qualification /Audit of CxP Vendors and CxP service providers • Responsible for GxP Training • Responsible for providing all documentation and other necesary support for Regulatory for product registrations and life cycle management • Responsible for providing all documentation and other necessary support for Business / Marketing, Customers • Responsible for management of Deviations, OOS, Complaints, Changes, Qualifications, Validations • Responsible for Licenses, Certifications and compliance (Indian FDA / CDSCO)