2368 Qms Jobs - Page 4

About Company Founded in 2011, ReNew, is one of the largest renewable energy companies globally, with a leadership position in India. Listed on Nasdaq under the ticker RNW, ReNew develops, builds, owns, and operates utility-scale wind energy projects, utility-scale solar energy projects, utility-scale firm power projects, and distributed solar energy projects. In addition to being a major independent power producer in India, ReNew is evolving to become an end-to-end decarbonization partner providing solutions in a just and inclusive manner in the areas of clean energy, green hydrogen, value-added energy offerings through digitalisation, storage, and carbon markets that increasingly are integral to addressing climate change. With a total capacity of more than 13.4 GW (including projects in pipeline), ReNew’s solar and wind energy projects are spread across 150+ sites, with a presence spanning 18 states in India, contributing to 1.9 % of India’s power capacity. Consequently, this has helped to avoid 0.5% of India’s total carbon emissions and 1.1% India’s total power sector emissions. In the over 10 years of its operation, ReNew has generated almost 1.3 lakh jobs, directly and indirectly. ReNew has achieved market leadership in the Indian renewable energy industry against the backdrop of the Government of India’s policies to promote growth of this sector. ReNew’s current group of stockholders contains several marquee investors including CPP Investments, Abu Dhabi Investment Authority, Goldman Sachs, GEF SACEF and JERA. Its mission is to play a pivotal role in meeting India’s growing energy needs in an efficient, sustainable, and socially responsible manner. ReNew stands committed to providing clean, safe, affordable, and sustainable energy for all and has been at the forefront of leading climate action in India. Job Description Designation : Deputy Manager Experience : 5 years ~ 8 years Education : B. Tech - Full-time (Electrical/EE/ EEE) Knowledge of contractor assessment Interaction with 3rd party inspection agencies Monitoring of work done by 3rd party engineers Knowledge of ISO 9001 requirements. Knowledge of preparation and verification of RCA and Corrective actions. Imparting Job specific trainings. Knowledge of the various standards applicable in Solar/Power installations. Knowledge about testing and commissioning. Preparation of Field Quality plans, SOP’s ,Work instructions. Please note: This job requires travel, 3 days to 4 days in a month.

To head and manage Quality function across Suppliers, Processes and Customers. Will handle Quality Assurance Strategy for Supplier / Manufacturing value chain for continuous improvement of Overall Quality Metrics etc.

The Quality Coordinator reports directly to the Associate Quality Excellence, assists in the development of, and responsible for the maintenance, control of documents and continual improvement of the Quality Management System (QMS) and Business Management System (BMS). The Quality Coordinator assists in the preparation and administration of all Quality Management System related matters and liaises with colleagues across the business in cross referencing of all documentation pertaining to QMS/BMS. Responsibilities Maintenance and management of Business Management System (BMS) SharePoint site. Updates and maintains files, logs, including Master Document List (MDL) Revises and/or creates document in the Management system as required. Possesses a professional and confident manner. Point of contact for all document creation and/or revision. Performs administrative support of the QMS/BMS. Obtains required approvals/signatures as required for Plans/Procedures and documentation. Manages the Documentation Creation/Revision requests and system. Ensures Quality Control of documents and records are maintained in accordance with the approved quality procedures. Ensures electronic distribution of Management system when required. Checks, verifies, and confirms the QMS status for the business. Behaves in a way that is consistent with WSP s values - honesty and integrity. A positive attitude with a strong work ethic is key. Supports the team in document and reports formatting. Mandatory Skills 1. O365 Applications including MS Office (Word, PowerPoint, Excel), MS Team, Outlook) 2. 2 years experience in SharePoint 2010/2013 or above 3. Ability to troubleshoot SharePoint 2010/2013 4. Good communication and interpersonal skills. 5. Time Management

What You'll Do Daily confirmation of open PO for DC Project Sales Impact by sites based on shortages & past dues Track OH versus requirements by site to track risk Work with suppliers to gather potential substitutes of the material that are short. Demand Planning, PO creation and timely PO acknowledgement & follow up with suppliers; Manage open POs through confirmations for deliveries, updating ERPs and manging orders till delivery Meeting the SLAs as defined; Creating and timely upgrading the SOPs and other related documents, meeting QMS requirments; Timely resolution of On Hold invoices for the various sites working closely with site, suppliers, IM team; Day to day communication with various stakeholders like Site Buyers,SCM Manager,Suppliers with timely actions and resolutions, attending site tier meeting . Working Knowledge of ERP; Mapics, Vista preferred Negotiation skills will be an added advantage; Knowledge on cost analysis, ROP & Planning parameter analysis; Should have hands on experience of Part Rationalization, Standardization; Sound knowledge of End to End P2P cycle, Product Costing & Manufacturing Processes; Should be able to analyze opportunity, initiate and execute projects to achieve Cost Out/Saving, Productivity Targets. Proficient knowledge on SCM functions. Qualifications Graduate in Engineering or Equivalent/ Post Graduate in any stream.

Role & responsibilities Position Sr. Exe. / AM- Quality (QMS* Industry automotive *Email jobpune2025@gmail.com * *Location Pune chakan Bhamboli* *Contact -9356395439* *Experience* - 5 to 8 yr. *Qualification* BE / Diploma *CTC- 6-8 LPA* Job Profile – 1. Knowledge of Quality Standards, 2. Internal and external audit planning, execution, and reporting 3. Ability to perform risk assessments. 4. Knowledge of preventive and corrective action processes 5. *Six Sigma, Lean, Kaizen, 5S, PDCA* , root cause analysis 6. Mastery of document management systems 7. Knowledge of change control procedures.

Job Title: Sr. Executive/ Asst. Manager- Corporate Quality Assurance (CQA) Department: Quality Assurance Industry: Pharmaceuticals Location: Based in Mumbai (Requires Traveling within India) Reports to: Management Job Purpose: To ensure consistent quality across all pharmaceutical manufacturing processes and sites by implementing and monitoring corporate-level quality systems and regulatory compliance. This role supports global compliance, audits, and continuous quality improvement activities in accordance with cGMP, ICH, US FDA, EU, MHRA, and other regulatory standards. Key Responsibilities: 1. Quality System Oversight Monitor and evaluate the implementation of Quality Management Systems (QMS) at manufacturing sites. Support the development and revision of corporate quality SOPs. Review and approve site-specific SOPs to ensure alignment with corporate quality policies. 2. Compliance and Auditing Conduct internal and external GMP audits (vendors, third-party manufacturers, CMOs). Track and ensure closure of audit observations and CAPA implementation. Assist in regulatory inspections and respond to regulatory queries. 3. Documentation and Review Review and approve key quality documents: BMR/BPR, validation protocols, change controls, deviations, and OOS investigations. Ensure compliance with data integrity requirements. 4. Training and Development Provide training to QA teams on corporate policies, data integrity, and regulatory requirements. Support continuous improvement and knowledge sharing initiatives across the organization. 5. Regulatory Support Participate in dossier review for regulatory submissions (ANDA, NDA, MA). Support QA due diligence for new product launches and tech transfers. 6. Risk Management & Quality Metrics Evaluate quality risks and trends across sites using KPIs and metrics. Prepare and present periodic quality performance reports to senior management. Qualifications and Skills: Education: B.Pharm/ M.Pharm / M.Sc. in a relevant field. Experience: 34 years in Quality Assurance, with exposure to corporate QA or multi-site operations. Technical Skills: In-depth knowledge of GMP regulations (ICH, US FDA, EU, WHO, etc.) Experience in auditing, CAPA, QMS, and regulatory inspections Strong documentation and analytical skills Proficient in MS Office Soft Skills: Strong communication and interpersonal skills Problem-solving and decision-making abilities Attention to detail and high ethical standards Preferred Certifications (optional): Certified Quality Auditor (CQA – ASQ or equivalent) Role & responsibilities Preferred candidate profile

Implement & Maintain QMS for IATF, ISO 14000, ISO 45001, VDA6.3, IMDS etc. MRM / Internal Audits, prepare & Conduct Mgmt. Reviews as per plan. Help process owner in preparing Manual, process approach, Work Instruction, Check Sheet Records etc. Required Candidate profile BE / Diploma Mechanical with 9 - 13 yrs exp. in Quality Management System from Automotive Industry. Supplier Process Audit, System Audit and control supplier PPM. Prepare PPAP documents for NPD etc.

Job Title : Assistant Manager Or Deputy Manager Job Location : Hyderabad Department : QA Reports to : HOD Job Objective : To perform the QA activities in view of system upgradation and improvement in the existing procedures. Job Role: 1. Execution & co-ordination for investigations, Identification of root cause along with assignment of adequate CAPAs for Returned material, Incidents, Deviation, OOS, OOT, complaints & other quality events. 2. Logging, Review & Closing of the change controls and CAPAs along with implementation of CAPA and its effectiveness verification as applicable. 3. Responsible as site representative during Regulatory Audits and customer inspections to co-ordinate with the Inspectors /Auditors. 4. Preparation & review of quality risk assessment reports of products & general systems 5. Conduct on the Job Training and cGMP trainings. 6. Implement documentation system to develop, maintain, distribute and control of all Quality Control, Quality Assurance, Production, Maintenance and Warehouse records. 7. Planning & execution of internal quality audits and perform vendor audits for the KSMs and packaging materials for vendor qualification. 8. Co-ordination with the customer for compliance and day to day issues. 9. Quality agreements review and preparation. Job Qualification: Masters in Chemistry (Any specialization) Job Experience: 10 to 12 years Desired attributes: Technical / Functional: Should have exhaustive knowledge on the drafting skills (E.g. Investigations, Responses & compliance). Should have sound command on the English with speaking and Writing. Sound knowledge of the production operations, QC analytical techniques & facility and maintenance functions. Behavioral: Team management, Leadership, Project management, Proactive, Time management and Critical thinker.

Specifying quality requirements of raw materials with supplier Investigating and setting standards for quality and health and safety Ensuring that manufacturing processes comply with standards at both national and international level Required Candidate profile Working with operating staff to establish procedures, standards, systems and procedures Writing management and technical reports and customers charters.

Rushabh Industries is a leading manufacturer of domestic and agricultural pumpsets, offering tailored pumping solutions for various applications. Established in 2000 and headquartered in Ahmedabad, India, the company operates two manufacturing units in Odhav and Sanand. Combining decades of industry experience with modern engineering, Rushabh Industries produces high-quality, durable products. Serving multiple industries including dewatering, agriculture, residential, and waste management, their extensive product range includes dewatering pumps, wastewater and sewage pumps, centrifugal pumps, self-priming pumps, openwell submersible pumps, and vertical submersible pumps. In the role based in Sanand GIDC, Ahmedabad, as a Quality Manager at Rushabh Industries, you will be responsible for leading and managing the Quality function and teams across the plant. Your key responsibilities will include overseeing Incoming Quality Control (IQC), In-Process Quality Control (IPQC), and Outgoing Quality Control (OQC) to ensure product conformance for regular and new products. You will also be tasked with deploying and optimizing Inspection Activities, managing in-house calibration activities for instruments and gauges, and analyzing quality data using advanced analytical tools such as SPC, DOE, FMEA, and Root Cause Analysis. Furthermore, you will be expected to support PPAP, FMEA, SPC, Product, Process & System audits, develop, implement, and manage the Quality Management System (QMS) to meet company and industry standards, design and support the creation of SOPs and Work Instructions for processes and operations, handle customer concerns and claims with timely resolution and root cause analysis, monitor and improve KPIs to ensure compliance with quality standards and efficiency goals, and develop and implement quality strategies aligned with customer requirements. As a Quality Manager, you will lead a team of QC engineers and inspectors, act as the point of contact for all customer quality concerns and audits, maintain quality documentation per QMS requirements, track and report quality KPIs including PPM, rejection %, rework %, audit scores, etc., utilize 7 QC tools and CAPA/critical analysis of process and product to improve quality, and lead continuous improvement initiatives such as Lean, Six Sigma, and Kaizen to enhance product quality and reduce process variation. To excel in this role, you should possess key skills in Quality Management, Root Cause Analysis, QMS, Process Quality Assurance, Supplier Quality Assurance, CAPA, Why-Why Analysis, Customer Complaints Analysis, Manufacturing Quality Analysis & Improvement, as well as excellent problem-solving and team management abilities. A Bachelor's degree in Engineering, Quality Management, or a related field is required, along with 4 to 9 years of experience. Experience in the pump manufacturing or related industry is a plus, and the ability to work on-site in Sanand and lead a team effectively is essential.,

Responsible for leading production operations, coordinating production staff and equipment, ensuring product quality and profitability, and overseeing and managing the production operations involved in injectable products.

Vendor Management Selection of the necessary vendor, Management and coordination of the same from development to 1 st production Finalize BOM (Bills of Material) Nominate Raw Material Suppliers Negotiate Raw Material prices Finalization of Finished goods Prices Coordination Finalize and coordinate Samples with Design Team and Marketing Coordinate with the quality team for testing and inspection of finished goods and Raw Materials Education Graduate/ Post Graduate (Added advantage) Experience Requirements 6 Years of Relevant experience Quick learner & ability to Multi-Task Experience in Vendor management is an added advantage Good knowledge of Materials and Technical Requirements

Job Description Summary In this role you will develop and maintain systems, rules, and processes to ensure fulfillment of internal and external requirements. You will ensure that projects and products are capable and will meet specified standards (Preventive). You will have In-depth understanding of key business drivers; uses this understanding to accomplish own work. You will ensure each project is developed & released meeting customer expectations and regulatory requirements . GE Healthcare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world. Job Description Roles and Responsibilities 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. Supports continuous product and process improvement through detailed failure analysis for nonconformances, and investigates, develops and implements effective and compliant solutions for product or process corrections, retrospective and remediation action plans, and for corrective and preventive actions (CAPA Program). 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. Required Qualifications This role requires advance experience in ISO 13485 and SDLC 62304 domain in a regulated industry (such as FDA, EUMDD/MDR Demonstrated knowledge on cybersecurity and privacy regulations. Knowledge level is comparable to a Bachelors degree from an accredited university or college ( or a high school diploma with relevant experience). Minimum Years of experience in the relevant industry - 5 to 10 Years or more Desired Characteristics Strong oral and written communication skills. Demonstrated ability to analyze and resolve problems. Demonstrated understanding of Medical Device QMS requirements and regulatory requirements including but not limited to ISO 13485 and FDA 21 CFR 820. Inclusion and Diversity We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership always with unyielding integrity. Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you d expect from an organization with global strength and scale, and you ll be surrounded by career opportunities in a culture that fosters care, collaboration and support. Relocation Assistance Provided: No

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.

Quality Engineer Reports To : Quality Manager About AeroCision Aerocomp India Pvt Ltd (AeroCision India) : AeroCision India ( ACI ), is an AS9100 Rev D certified aerospace factory based in Bangalore. ACI started operations in 2013, since then we manufacture complex machined turbine engine parts using proven world class Quality and Production systems. ACI has a track record of for the best Quality, Cost and Delivery. Job Summary : We are seeking a highly motivated and experienced Quality Engineer to join our growing team. The successful candidate will play a crucial role in ensuring the quality and compliance of our aerospace products and processes, with a strong focus on AS9100 Rev D standards. Responsibilities : Quality Management System (QMS) Implementation and Maintenance: Lead the implementation, maintenance, and continuous improvement of the QMS in accordance with AS9100 Rev D requirements. Ensure compliance with all applicable regulatory requirements (e.g., FAA, EASA). Develop, review, and maintain quality manuals, procedures, work instructions, and other quality documents. Conduct internal audits and participate in supplier audits to assess and improve quality performance. Non-Conformance and Corrective/Preventive Action (CAPA): Investigate and analyze non-conforming material and processes. Lead the implementation of effective corrective and preventive actions to address root causes and prevent recurrence. Track and monitor the effectiveness of CAPA activities. Product and Process Quality : Review and approve engineering drawings, specifications, and other technical documents. Monitor and analyze process performance data to identify areas for improvement. Conduct root cause analysis of quality issues and implement corrective actions. Support production operations to ensure product quality and process compliance. Metrology and Measurement : Ensure the accuracy and calibration of all measuring and test equipment. Develop and maintain calibration procedures and schedules. Investigate and resolve measurement system variations. Train operators on the proper use and care of measuring equipment. Customer Satisfaction : Interact with customers to address quality concerns and build strong relationships. Analyze customer feedback to identify areas for improvement. Support customer audits and resolve any quality-related issues. Continuous Improvement : Identify and implement process improvements to enhance efficiency and reduce costs. Participate in Lean Six Sigma or other continuous improvement initiatives. Stay abreast of industry best practices and regulatory changes. Qualifications : Bachelor s degree in Engineering (Aerospace, Mechanical, or related field) Minimum 5 years of experience in a Quality Engineering role within the aerospace industry Strong understanding of AS9100 Rev D requirements Proven experience in implementing and maintaining a robust QMS Knowledge of various quality tools and techniques (e.g., FMEA, SPC, 8D) Proficiency in using metrology equipment (e.g., CMM, calipers, micrometers) Excellent analytical, problem-solving, and communication skills Strong attention to detail and organizational skills Ability to work independently and as part of a team Preferred Qualifications: Lean Six Sigma certification Experience with ERP/MRP systems Knowledge of other relevant industry standards (e.g., ISO 9001, NADCAP) To Apply : Please submit your resume and cover letter to Equal Opportunity Employer : AeroCision Aerocomp India Pvt. Ltd. (ACI) is an equal opportunity employer and values diversity. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation. age, marital status, veteran status, or disability status. Job Category: Quality Job Type: Full Time Job Location: Bengaluru Apply for this position Full Name * Email * Phone * Cover Letter * Upload CV/Resume * Upload CV/Resume * Allowed Type(s): .pdf, .doc, .docx By using this form you agree with the storage and handling of your data by this website. *

Develop and maintain QMS documentation. Conduct internal audits and support external audits to ensure compliance. Initiate and track corrective and preventive actions. Ensures compliance As per the industry standards (ISO)

Responsibilities: * Execute CapA activities and document results. * Ensure quality compliance through ISO documentation. * Collaborate with production team on product improvements. * Conduct regular audits using QMS principles. Provident fund Annual bonus

We are conducting Walk-in Interview at Indore for our OSD manufacturing Facility based out of our Ahmedabad (SEZ-II), please find the below details. Date : 27th May 2025 (Sunday) Interview Location: Ahmedabad Timings: 9:00 am 5:00 pm Interview Venue: PTC-Sigma Block No. 2, 3, 4, 5, Sigma Commerce Zone,Nr Iskon Mandir BRTS Bus Stand, Ambli Bopal Road, Ahmedabad – 380015 ? Job Location: Ahmedabad Education Qualification: ITI/Diploma/BSC/ /B.Pharma Departments are as follows : Production- OSD : Plant Operator/ Technical Assistant : ITI / Diploma having 3 - 8 years of experience in operating machines like Granulation (ACG, Glatt, Tapasya, GEA), Fitzpatrick Roll Compactor, Compression machines (Fette), Wurster Coater (ACG, Glatt, Anish), imprinting, Visual Inspection. Perform line clearance, operation and cleaning of equipment / instrument / auxiliary items Executive/ Sr Executive: B. Pharma with 3 - 8 years of experience in Tablet/ Capsule department with experience in Granulation, Compression, Coating, Inspection . Responsible to plan for the manufacturing of batches in coordination with PPMC. To monitor line clearance, cleaning of equipment, instrument, auxiliary items. To carry out qualification activities. To initiate QMS activities (Change control, deviation, CAPA, investigation) and E-BMR. To handle manpower and allocate daily activities.. Engineering: Technician : Diploma / ITI with 3- 8 years of experience in plant maintenance & Process Equipment (Electrical/ Instrumentation) and Instrumentation . Candidates should have experience in Plant maintenance, preventive maintenance and breakdown maintenance of OSD plant equipment. Troubleshooting of mechanical and electrical equipment . Instrument and calibration of OSD plant equipment. They should have knowledge and experience in instruments sensors, PLC, HML, SCADA, and experience in calibration activities. Quality Assurance (Qualification) Assistant Manager / Deputy Manager / Associate Manager: B.Pharm with 10-20 years QA & MFG – Qualification. Candidates should have experience in Qualification, Validation. They would have to prepare, execute and review of equipment/ instrument/ system /utility /area qualification program. Review of data backup activity, data restoration and its compliance. QMS documentation exposure is required. completion of CAPAs and to perform change control/CAPA effectiveness. Associate Manager: CSV B.Pharm with 15-20 years with experience in Issuance and retrieval of documents. Candidate should have experience in Review of various Qualification and CSV Documents. Review of system audit trail, system security user privileges and ensure the compliance. Review of data backup activity, data restoration and its compliance. To ensure timely completion of CAPAs and to perform change control/CAPA effectiveness. For all the positions, candidate should have exposure in pharmaceutical company and exposure to regulatory requirements of documentation and cGMP will be added advantage. Interested candidates Please Walk-in for an interview along-with their Aadhar Card, Passport size Photograph, updated CVs, Salary Structure, Salary Slip and relevant documents(original as well as Photocopies) as per the schedule.

1.Lead & oversee the QMS activities to ensure compliance with cGMP & regulatory requirements 2.Manage lifecycle of quality documents: SOPs, change controls, deviations, CAPAs, risk assessments 3.Conduct training programs on QMS and compliances Required Candidate profile 1. Job Location is Chengalpet 2. Bachelor’s or Master’s degree in Pharma 3.10–15 yrs of exp in managing QMS function in pharm formulation 4. Knowledge of regulatory guidelines cGMP, ICH, WHO, EU-GMP

You will lead the Plant Quality department and ensure smooth execution of all Quality functions. Your responsibilities will include reducing PPM/Defects across all Quality areas, maintaining existing quality system standards such as IATF-16949, ISO 9001-2015, etc. You will be hands-on with Quality KPIs and ensure Quality Objectives are met. Conducting Supplier Audits to reduce rejection/defects and meeting Customer Expectations for quality products and documentation, leading customer and Certification Audits will also be part of your role. Additionally, you will be responsible for maintaining 5S, Kaizen practices, and identifying training needs. You will oversee the internal team members in performing Quality Activities as per requirements. Your active participation in FT activities to enhance organizational operations will be essential. A good understanding of ERP and QMS is required for this role. This is a full-time, permanent position with benefits including health insurance, leave encashment, and provident fund. The work schedule is during the day shift, and the preferred education requirement is a Diploma. The work location is in person.,

As a candidate with experience in the injection moulding industry, specifically in manufacturing spouts, caps, and closures for the food and beverage sector, you will be responsible for various key activities within the organization. You will be tasked with the overall monitoring and control of day-to-day departmental activities. This includes overseeing all incoming raw materials, in-process manufacturing, and final product quality to ensure compliance with established systems. Your role will involve regular interaction with internal and external stakeholders to ensure that production outputs meet the required standards in a timely manner. Additionally, you will be responsible for addressing customer queries and managing complaints effectively to enhance overall customer satisfaction. You will play a crucial role in coordinating internal, external, and customer audits to ensure that the organization maintains necessary certifications and standards. Compliance with quality management systems and food safety regulations will be a key focus area for you. Furthermore, you will be responsible for preparing daily and monthly reports related to plant operations and ensuring their timely circulation. Identifying any skill gaps at the operational level and arranging appropriate training sessions, both internally and externally, will be part of your duties to enhance awareness and knowledge among the team.,

As an experienced Inspector, you will be responsible for reviewing contractual requirements such as technical standards and specifications, identifying any execution or inspection issues that may arise. Your primary duties will involve the inspection of Pressure Vessels and components including Filters, Boilers, Storage Tanks, etc. You will oversee the inspection process from the raw material stage to the final stage, ensuring compliance with codes and standards like ASME Sec-VIII. This will involve reviewing documents like QAP, WPS, PQR, WPQR, NDT procedures, material identification, applicable testing, and conducting stage-wise inspections of welding and fabrication processes. In addition to Pressure Vessels, you will be involved in inspecting Piping systems for Process Plants. Your responsibilities will include conducting stage-wise inspections, components inspections, dimensional checks, and spool inspections at fabricators" sites. You will also be tasked with inspecting Pipes & Tubes, following ASTM, IS, and API standards from the raw material stage to the final inspection. This will involve reviewing documents, conducting various tests such as U.T., Eddy-current testing, MPT, Hydro-test, mechanical tests, and ensuring compliance with different grades. Furthermore, you will be responsible for inspecting piping components like Flanges, Fittings, Valves, Pumps, and conducting various testing activities as per applicable piping codes and product standards. Your expertise will also be required in the inspection of Castings, particularly critical components like Shafts, Roller assemblies, Gears, Mill Heads. This will involve activities such as Raw Material Identification, physical & chemical testing, U.T., M.P.I., D.P.T., and final inspections after machining. Moreover, your role will include inspecting Steel structures for hydro power plants, focusing on structural parts of hydropower projects such as radial gates, surge shafts, trash racks, as well as other structural elements like trusses and towers. You will be responsible for selecting the most appropriate inspection techniques, coaching and supervising inspectors, conducting vendor assessments, and managing project coordination. Your expertise will be crucial in preparing and implementing inspection checklists, coordinating and managing projects for inspection of bought-out items, site inspections, and fabricated structural parts. Your attention to detail, knowledge of codes and standards, and ability to ensure compliance with quality control and quality assurance requirements will be essential in this role.,

Roles & Responsibilities: Preparation and timely update of Technical Files Regular updating of the Quality Manual Review and update of all relevant Standard Operating Procedures (SOPs) Review and revision of Work Instructions as per process requirements Preparation of Marketing Support Documents from QA perspective Review and update of internal Formats and Templates Periodic review and update of Site Master Files Must have working knowledge of various audits related to the medical device industry , including ISO 13485 , MDSAP, and CDSCO inspections

Roles and ResponsibilitiesPreparation and training to Engineers/DETs/Associates about outgoing quality control plan, visual inspection procedures, AQL based inspection plan etc.Clearance of finished good in SAP as per FQA plan and maintain daily reports/records/MISRejecting and returning non-conforming materials to production department for rework/final rejects.Maintain documents of Inspection, reworks, AQL, defects trends analysisMaintain safe and healthy work environment by following defined standards and procedures.Regular feedback to production department about NCs observed and ensure their closures.Issue of SLN (Stop line note) in case of producing non-conformance materials or not following defined SOPs, and control plan and their closures.Handle internal and external CCRs and their closure as per defined SLAs.Ensure CAPA effectiveness for all the complaints by regular audits.Support production and process department in improvement of quality or cost reduction projects.Support packing and dispatch team in improving existing packing material, new packing material design and development to improve quality and cost reduction.Prepare samples for any new customers along with test reports.Quality improvement by working closely with customers by their feedback and requirements.Maintaining limit samples for all type of defectsBenchmarking of cells specifications with other cells in marketClearance of FG in SAP as per SLAs.Coordinate for PDI for customer at shop floor/FG storPrepare samples for reliability tests like PID/LID/Rip-Off/Soldering peel test or any other test as per IEC certification.Profile & Eligible Criteria6-8 years of experience in solar cells manufacturing with preferably in FQA functionDiploma/B.Tech/M.Sc.preferably in electronics

VACANCY FOR QUALITY ENGINEER We are seeking a highly skilled Quality Engineer to ensure defect free supplies to customer by Quality control of Industrial Oil Cleaning skids, Fuel conditioning Modules, Heat Exchanger skids, Pumping skids etc built in Industrial Module Factory (IMF) for Energy, Oil & Gas, Marine and Diesel Power sectors as per approved drawings, standards and customer requirements. About the Company: In Alfa Laval, Every day, we get opportunities to make a positive impact on our colleagues, partners, customers and society. Together, we re pioneering the solutions of the future and unlocking the full potential of precious resources. Trusted to act on initiative, we challenge conventional thinking to develop world-leading technologies that inspire progress in vital areas, including energy, food, water and shipping. As we push forward, the innovative, open spirit that fuels our 140-year-old start-up culture and rapid growth also drives our personal growth. So, as we shape a more resourceful, less wasteful world, we build our careers too.. Please feel free to peruse our website www.alfalaval.com . The position / About the Job: Job Description Understanding Customer, Drawing, and standard requirements for Fabricated, machined, electrical, and other components in the modules/skids and converting to Quality Assurance Plan. Inspection of components at receipt stores, shopfloor or at Vendors premises as per the Quality plan/ drawing/ data sheet. Identifying Non-conforming Product and Process at the shopfloor and the Supplier. CAPA for Non-Conforming Product, Process. GRIR Clearance in Movex ( ERP). Supplier Evaluation and Audit for continual Improvement. Inspection Reports at the Intermediate and Final Stage as per standard and Customer requirements. Coordination with internal and external customers. NDT Inspection and Report preparation. Making procedures, Work Instructions as per Technical and QMS requirements. Co-ordination with Testing and Calibration Labs. EMS & OHSAS Requirements: Safety awareness for welding as per EMS and OHSAS. Ensure use of required PPE during shop round/ vendor visits. Qualification, Knowledge and Skills: BE ( Mech ) with 5 to 6 years experience. NDT Level II qualification Sound technical Knowledge of Piping, Welding, Machining, and Fabrication Process. Sound technical Knowledge of ASME and EN Standards and Material Standards Good knowledge of Inspection and Testing instruments and their usage. Should be aware of Lab Testing methods and standards. QMS ISO 9001:2008 system and documentation awareness. Attitude and motivation: Good communication skill with third-party inspectors and customers Must be a flexible team player with good communication skill. Positive attitude. Decision making by taking into consideration experience and good engineering practices Why should you apply We offer you an interesting and challenging position in an open and friendly environment where we help each other to develop and create value for our customers. Exciting place to build a global network with different nationalities to mingle and to learn. Your work will have a true impact on Alfa Laval s future success, you will be learning new things every day. Interested? Please apply for the position Note - We care about diversity, inclusion and equity in our recruitment processes. We also believe behavioral traits can provide important insights into a candidates fit to a role. To help us achieve this we apply Pymetrics assessments, and upon application you will be invited to play the assessment games.