Dear Candidates, Greetings from KEYBIZ DASHBOARDS, We are looking for Quality Assurance Executive & Sr.Executive injectables&OSD for one of our reputed pharmaceutical client, based at Hyderabad & Vizag location. Please find below openings list. 1.IPQA 2.QMS 3.AQA 4.Validation 5.Equipment Qualification 6.CSV 7.Market Complaints. The above positions we are looking for Hyderabad & Vizag locations, interested please share us updated cv to prasanthi@mydashboards.in or feel free to call on 6305391924 Thanks and Regards Prasanthi - Dashboards Team HR

We are looking for a highly skilled and experienced Operations Analyst to join our team at Equitas Small Finance Bank Ltd. The ideal candidate will have 2 to 7 years of experience in document verification and be able to work efficiently in a fast-paced environment. Roles and Responsibility Verify documents for accuracy and completeness. Perform quality checks on verified documents. Collaborate with the operations team to resolve issues. Develop and implement process improvements to increase efficiency. Maintain high customer satisfaction through excellent service. Ensure compliance with regulatory requirements. Job Requirements Minimum 2 years of experience in document verification or a related field. Strong knowledge of document verification processes and procedures. Excellent analytical and problem-solving skills. Ability to work effectively in a team environment. Strong communication and interpersonal skills. Proficient in Microsoft Office and other software applications.

We are looking for a highly skilled and experienced Branch Manager to lead our Mutual Funds team in Equitas Small Finance Bank Ltd. The ideal candidate will have a strong background in BFSI, particularly in mutual funds, with 2-7 years of experience. Roles and Responsibility Manage and oversee the daily operations of the branch's mutual funds department. Develop and implement strategies to boost sales and revenue growth. Lead and motivate a team of professionals to achieve business objectives. Build and maintain relationships with key stakeholders, including clients and partners. Ensure compliance with regulatory requirements and industry standards. Analyze market trends and competitor activity to stay ahead in the market. Job Requirements Strong knowledge of mutual funds products and services. Excellent leadership and management skills. Ability to drive sales and revenue growth. Strong communication and interpersonal skills. Ability to work in a fast-paced environment and meet deadlines. Any graduate degree from a recognized university.

Roles and Responsibilities Calibration Principles Material Handling & Safety Awareness Measuring Equipment Handling MSA Calculations in Calibration Calibration Frequency Monitoring Traceability for Calibration (NABL) Calibration Terminologies (Resolution, Least Count, off Set, Accuracy, Uncertainty, Error.. 6s & ESD QMS Procedures Trained in QMS Standard Audit Principles Audit Procedures and Methods Core Tools Understanding of Customer Specific Requirements Communication Skills Problem Solving Technique Skills Required Minimum 3 yrs experience in EMS Knowledge in Quality system procedure and Calibration activity. Must have: Good communication. Good to have: Owner ship and Responsible in the assigned activity About Company: Avalon provides solutions in manufacturing from design, analysis to mass production . We provide our customers with integrated manufacturing facilities, skilled workforce, certified quality systems and a network of supplier partners to deliver quality products and services on time. The group today is a preferred supplier to worlds leading companies, viz., Alpha, Kyosan, Alstom, Robert Bosch, Continental, Tesla, Cummins etc. in the ESM and in aerospace business. The Avalon group is an INR 867 Crore revenue (FY 23 - 24) enterprise while ATPL along with other Indian group companies (ATS and Sienna ECAD). The group has a well-rounded professional team across USA & India with employee strength of 2000+ (in US & India). The group has an excellent track record of 20+ years with a thorough list of customers predominantly in US and growing list in India.

At Capgemini Invent, we believe difference drives change. As inventive transformation consultants, we blend our strategic, creative and scientific capabilities,collaborating closely with clients to deliver cutting-edge solutions. Join us to drive transformation tailored to our client's challenges of today and tomorrow.Informed and validated by science and data. Superpowered by creativity and design. All underpinned by technology created with purpose. The GxP CSV Validation Engineer ensures that digital systems used in clinical development comply with regulatory standards (GxP, 21 CFR Part 11, EMA Annex 11). They develop and execute validation protocols (IQ, OQ, PQ), risk assessments, and documentation to support system compliance and audits. The GxP CSV Validation Engineer ensures that digital systems used in Clinical, Regulatory Affairs, Medical Affairs, and PV Safety comply with GxP, 21 CFR Part 11, EMA Annex 11, and other regulatory standards. They develop and execute validation protocols (IQ, OQ, PQ), perform risk assessments, and maintain compliance documentation. Primary Skills Bachelors or Masters degree in Life Sciences, Computer Science, Regulatory Affairs, Quality Assurance, or a related field Certifications such as Certified Quality Auditor (CQA), GAMP 5, or CSV-related certifications are advantageous Skills (competencies)

The Quality Process Professional establishes and runs the quality process. They have various responsibilities which include architecting, defining and maintaining Quality Management Systems to enable standard way of working, developing and managing process assets methods, PoVs best practices, enablers to facilitate delivery and acting as SMEs in areas such as Agile, Service Management, Six Sigma etc. They are responsible for creating and maintaining process metrics baselines and prediction models accountBU level to support data driven delivery execution and governance and support creation of estimation models. They will plan and drive external quality certification initiatives to provide confidence to internal external stakeholders on the robustness of QMS and plan and conduct Quality Audits to monitor compliance, provide early alerts, identify best practices and improvement opportunities. The Quality Process Professional will also develop and conduct Quality trainings to enhance awareness and skills and enable the sales function by creating assets highlighting Capgeminis processes, process assets and platforms. They can also be called upon to assist with solutioning as Subject Matter Experts. - Grade Specific Quality Process ConsultantSupport process definition and maintenance, process assets development, process metrics baselines and prediction models, quality certifications, quality trainings and audits Skills (competencies) Active Listening Adaptive Thinking Analytical Thinking Assertiveness Attention to Detail Business Agility Change Management Conflict Management Continuous Improvement Decision-Making Emotional Intelligence Financial Control Influencing Innovation Managing Difficult Conversations Negotiation Proactiveness Problem Solving Project Governance Project Management Project Planning Project Reporting Project Tracking Relationship-Building Risk Assessment Risk Management Scope Management Stakeholder Management Strategic Governance Strategic Thinking Team Management Time Management Unified Project Management (UPM) Unified Service Management (USM)

The Quality Process Professional establishes and runs the quality process. They have various responsibilities which include architecting, defining and maintaining Quality Management Systems to enable standard way of working, developing and managing process assets methods, PoVs best practices, enablers to facilitate delivery and acting as SMEs in areas such as Agile, Service Management, Six Sigma etc. They are responsible for creating and maintaining process metrics baselines and prediction models accountBU level to support data driven delivery execution and governance and support creation of estimation models. They will plan and drive external quality certification initiatives to provide confidence to internal external stakeholders on the robustness of QMS and plan and conduct Quality Audits to monitor compliance, provide early alerts, identify best practices and improvement opportunities. The Quality Process Professional will also develop and conduct Quality trainings to enhance awareness and skills and enable the sales function by creating assets highlighting Capgeminis processes, process assets and platforms. They can also be called upon to assist with solutioning as Subject Matter Experts. - Grade Specific Quality Management Risk and Compliance Officer Quality Audit Quality Management Skills (competencies) Active Listening Adaptive Thinking Analytical Thinking Assertiveness Attention to Detail Business Agility Change Management Conflict Management Continuous Improvement Decision-Making Emotional Intelligence Financial Control Influencing Innovation Managing Difficult Conversations Negotiation Proactiveness Problem Solving Project Governance Project Management Project Planning Project Reporting Project Tracking Relationship-Building Risk Assessment Risk Management Scope Management Stakeholder Management Strategic Governance Strategic Thinking Team Management Time Management Unified Project Management (UPM) Unified Service Management (USM)

Position: Senior Manager Sub-function: Global Actions Management Function: Corporate Quality Compliance Sub-function: Global Actions Management Function Head Title: Sr. General Manager Location: Vadodara Areas of Responsibility Ensure assessment of Regulatory inspection citations identified at Sunpharma sites to derive the global action Ensure assessment of 483s, warning letter issued to other organization by USFDA to derive the global action Ensure assessment of internal learning (such as Quality alert) to derive the global action Preparation of Global action based, following are the sub-activities: v. Review of the regulatory guidance related to the topic vi. Review of existing site practices vii. Drafting of Global action recommendations viii. Preparation of reference procedures and associated formats for Global action implementation as applicable ix. Finalization of Global action recommendation post review with Global action committee and relevant stakeholders Ensure issuance and approving of Global actions in Trackwise. Coordinating with sites for the implementation of Global action recommendations Ensure review of site action closure for completeness and correctness Ensure closure of global action upon completion of all issued site action records of a global action Ensure circulation of Global action status to relevant stakeholders Ensure compliance calls being executed as per pre-defined agenda i. e. internal and external learnings being shared and explained with stakeholders. o Ensure identified gaps being shared across sites and tracked for implementation Ensure maintenance of database for regulatory inspections at SUN Pharma Review of draft response of inspection observation Ensure Sun site regulatory inspection observations trend is in place for meaningful analysis All other duties as assigned by Head Corporate Quality Compliance and CQA Travel Estimate Approximate 30% Job Requirements Educational Qualification M. SC / M. Pharm Specific Certification Not specific Skills Quality Management System, Compliance, CAPA, Investigations, Audit Management, Supplier Qualification, Change Management, Manufacturing and Engineering Assurance (OSD and Sterile) Experience Minimum 15 years

Timely planning for the analysis of Stability Sample. T o ensure timely Stability samples Incubation. To maintain on line entry of stability data in summary sheet. On line Monitoring and data review of Stability Incubators. Stability Sample Analytical Trends. Stability Sample master updation, labeling, registration, charging and pullout. Timely initiation of QMS documents in track wise application and closure of action items. Regular review of SOPs versus practices for gap analysis. To perform investigations of respective OOS / OOT and UPDs.

Brief The Quality Engineer will provide FMEAs (Failure Mode and Effects Analysis) and Control Plans, drives Continuous Improvement, performs audits, ensures performance to workmanship standards. Investigates and leads Corrective Actions. Plans, implements, and coordinates applicable corrective, preventive and technical controls of processes and products as required. Develops and implements an effective quality system related to manufacturing elements; including, but not limited to quality planning, receiving inspection, and Quality Management System audits. Responsibilities: - Leads the identification of problem root cause and the development and implementation of effective corrections and preventive methods Participates in product and process development teams as applicable Analyzes various failure reports and recommends corrective action Collects, analyzes and reports on various measurement statistics and metrics Maintain an interactive plant quality relationship focused on effective transition of product releases to a manufacturing quality support role. Facilitate creation of control plans, process flows and Process Failure Mode Effect Analysis (PFMEA) specific to new product development. Interface closely with Engineering, Service, Manufacturing and Product Management to understand and improve product and service quality. Investigate and resolve QA projects, as assigned. Ensure communication and interaction with Supplier Quality. Participate as Auditor of the Vertiv Quality Management System. Other duties and responsibilities as assigned. Qualifications: - Minimum Job Qualifications: BA or BS or equivalent experience Bachelor of Science in Mechanical Engineering, Industrial Engineering, Industrial and Systems Engineering, or other relevant degree preferred No experience required with a bachelor s degree Minimum of 5 years relevant experience in lieu of degree Preferred Qualifications: Excellent communication skills, both written and verbal Proficient in MS office Ability to design special tooling, develop and manufacturing processes, and assess new manufacturing technologies Highly adaptable with the ability to learn and apply new skills quickly Possesses a strong work ethic and sets high standards for quality and quantity of work Education And Certifications: Bachelor of Science in Mechanical Engineering, Industrial Engineering, Industrial and Systems Engineering, or other relevant degree preferred Physical Requirements: - Heavy Lifting (over 50 Ibs. ) Frequent Standing Frequent kneeling / crawling / stooping Frequent bending / twisting Frequent climbing (stairs, ladders) Environmental Demands: - Protective Equipment Required (earplugs, gloves, eyewear, safety toed shoes/boots) Travel Time Required: - 10% domestic/international

Plant Process Architect, BBM QMS coordinator, Compass and Confluence expert, Plant Concession and risk assessment coordinator, Digital fluency - Data driven projects. coordinate as auditee for internal and external audits conducted by customer / certification body,

Handle QMS (ISO 9001: 2015), QC & Customer Assurance for Consumer Durable products Handle EMS (14001:2015) Be the Certified internal auditor for the both systems People & Process Mgmt. Quality Management OHSAS Six Sigma Lean manufacturing Required Candidate profile B.Tech 3-5 Years exp in QMS & EMS in manufacturing, engineering comp. QMS (ISO 9001 : 2015) CERTIFIED INTERNAL AUDITOR EMS (14001 : 2015) CERTIFIED INTERNAL AUDITOR Exp. in Six Sigma, TQM, OHSAS etc. Perks and benefits Best As Per Industry Standards

1 To ensure the 5S & Safety in the respective area. 2 To update the Control Plan, PFMEA or any other relevant documents as per the action plan submitted for any customer complaint or customer audit. 3 To prepare the PPAP documents in case of any ECN implemented. 4 To get the NCRs closed properly, raised during the audits. 5 To carry out the documentation related to EMS ISO 14001 : 2015 6 To ensure that shop floor documents (work instructions, Quality Plan etc.) are properly displayed & adhered. 7 To establish the required documentation of Quality system as per Standard IATF 16949:2016. 8 To give at least one suggestion in a month to optimize the use of consumables, electricity & raw material by doing VE (Value Engineering). 9 You are advised to present the Monthly Performance Report to the management on the basis of above mentioned points. Skills : - Internal Audit/ External Audit/IATF16949:2015/ ISO 14001:2015

Oversee the QC department, implement quality systems, ensure production meets standards, handle customer complaints, maintain documentation, lead audits, ensure ISO/regulatory compliance, and mentor the QC team for continuous quality improvement.

Role & responsibilities Develop and implement an integrated management system (IMS) that integrate quality management(ISO 9001), Environment management (ISO 14001), Occupational health and safety (ISO 45001), Energy management (ISO 50001) and asset management( 55001). Establish IMS policies, procedures and processes to ensure compliance with ISO requirement and regulatory. Experience in conducting internal audits, external audits and managing certification process. Coordinate with department heads to ensure alignments of processes and procedure with ISO requirements. Provide training and guidance to employees on IMS policies. Assuring safe work practice at workplace SAP Data entries related activity Proficiency in MS office suite and IMS software tools. Preferred candidate profile Candidates having experience of 4 to 8 years with Electrical Engineering background . Preference will be given to certification as ISO lead auditor.

Greetings from Dexcel Designs! Please find below the detailed JD for QA position with us. Job Title: Quality Assurance-Lead/Manager Location: Bangalore, India Job Summary We are seeking an experienced and detail-oriented Quality Assurance Manager to oversee and implement robust QA systems for our defence electronics manufacturing operations. The ideal candidate will have a deep understanding of Indian defence regulatory frameworks, MIL standards, and high-reliability electronics quality protocols. Responsibilities Lead the Quality Assurance function for defence-grade electronics systems including RF, embedded systems, and custom SoCs. Develop, implement, and maintain QMS in compliance with ISO 9001, AS9100D, and MIL-STD-810 / MIL-STD-461 / JSS 55555. Ensure adherence to DRDO, MoD, DGAQA, and BEL/ISRO quality requirements throughout the product lifecycle. Define inspection criteria for incoming materials, in-process assemblies, and finished goods using IPC-A-610, IPC-A-600 standards. Lead internal and external quality audits, including DGQA inspections, customer audits, and third-party certifications. Drive RCA (Root Cause Analysis) and CAPA (Corrective and Preventive Action) for product non-conformities and field returns. Coordinate with R&D and production teams to implement Design for Quality (DFQ) and Failure Modes and Effects Analysis (FMEA). Oversee quality documentation and traceability per defence contract requirements and maintain documentation for Defence & Aerospace projects. Maintain calibration, testing, and environmental compliance of lab/test infrastructure (EMI/EMC, vibration, thermal chambers). Provide QA input in supplier qualification, vendor audits, and strategic sourcing for high-reliability components. Train team members on quality tools (Six Sigma, 5 Why, 8D, FMEA) and ensure continual improvement. Required Qualifications B.E./B.Tech in Electronics/Electrical/Instrumentation Engineering (M.E./M.Tech preferred). 815 years of experience in Quality Assurance in defence, aerospace, or high-reliability electronics manufacturing. Strong understanding of Indian defence procurement processes, DGAQA, DGQA, CQAE, CEMILAC, RCMA procedures, and industry-specific compliance. Experience with ERP-based QA systems and electronic documentation management. Familiarity with cleanroom, ESD, and IPC standards. Certifications like Six Sigma Green/Black Belt, Internal Auditor ISO 9001/AS9100, preferred. Preferred Attributes Hands-on experience with defence-grade testing (EMI/EMC, ESS, HALT/HASS, burn-in). Exposure to product qualification under Make in India and IDDM schemes. Excellent communication, documentation, and leadership skills. Ability to engage with defence PSUs, MoD, DRDO, and system integrators.

Instrument Handling - pH Meter, Analytical Balance, Friability Tester, Disintegration Apparatus, Hot Air Oven, Moisture Balance, UV Sprct. Raw & Packing Material Testing Strong GLP Adherence Robust GMP Documentation Regulatory Compliance Awareness Required Candidate profile Experience: 2–3 years in pharmaceutical Quality Control Strong knowledge of analytical instruments and QC procedures Soft Skills: Detail-oriented, organized, good interpersonal & communication skills

Role & responsibilities Quality Standards Leadership : Lead the development and execution of robust quality standards across operations, ensuring 100% compliance with regulatory requirements and industry best practices. Alignment of Quality Functions : Harmonize efforts across In-process Quality Assurance, Quality Management Systems, Quality Control, and Quality Engineering to ensure seamless execution of departmental objectives aligned with business goals. Quality System Management : Oversee critical quality processes, including product complaints, CAPA, supplier quality, and internal audits, to ensure sustainable compliance with high-quality standards. Investigation Management: Conduct in-depth investigations into Out of specification Results, deviations, complaints, recalls, and stability failures, focusing on effective CAPA planning and implementation to mitigate risks. Responsible for review and approval of quality system documents such as; SOPs, specifications, Annual product quality review, Master batch manufacturing records, Master packing record and dispatch record, validation master plan, process validation documents, hold time study documents, cleaned and dirty equipment hold time study documents. Responsible for approval of changes to the existing systems, documents, processes, specifications, test procedures and ensuring change implementation. Responsible to monitor the compliance of standard operating procedure. Responsible for CAPA documents Review and Close out along with respective departments. Responsible to play a major role Implementation of cGMP practices in the facility. Responsible to regulatory audits / Inspections, customer audits and audit compliance. Responsible for Gap Assessment, impact assessment, development, and implementation of harmonized policies and procedures Responsible for Reviewing documents, Protocols, SOPs and Perform Gap assessment and harmonization of Procedures and Practices Responsible for review and integration of Quality Risk Assessment into Design and Qualification of Area, Equipment, Manufacturing Process, and Contamination control strategy Responsible for the preparation and training of quality policies & procedures Responsible for carrying out Audits and ensuring compliance. Also to work on the compilation of Quality Metrics, harmonization of the regulatory observations and follow up on compliance. Provide subject matter expertise to personnel on aspects of QMS systems and Compliance. Conduct internal and external audits as part of the Quality systems improvement program. Set, Maintain, and trend progresses related to Quality across site and provide performance indicators for senior management. All time readiness at the site for regulatory inspections in collaboration with Site management in the area of operation & quality area. Provide technical support during technical investigations, risk management exercises. Identify gaps/improvement areas in its solutions and implement at site. Design & execute continuous improvement initiatives within the region to enhance compliance, drive efficiencies & cost-effectiveness. Maintain a network of subject matter experts in facilities/utilities/process validation and provide support to site in the resolution of non-routine issues. Identifying the training needs of the teams and Conducting need base training programs. The interface between various customers and internal teams during technical presentations /technical gatherings. Preferred candidate profile

We are looking for Quality Head, who has worked at least 10years in SGI Casting speciality in Manhole cover division. Maintain QMS, with computer knowledge. Job location-Howrah(WB),Salary-35k-45k Monthly. Walk in Interview. Contact : +91 7687919790

Plant Head - Production Operation: About CMR CMR Group is India's largest producer of Aluminium and zinc die-castingalloys. With 13 state-of-the-art manufacturing plants across the country, CMRhas become the preferred supplier for many of Indias largest automotiveindustry leaders. Since its inception in 2006, CMR has consistently outpacedcompetition by focusing on delivering superior value to its stakeholders. Thisvalue is driven by a strong commitment to technical advancements, qualityenhancement, sustainability, and people-centric practices. We believe inan " Employee First " philosophy, ensuring that ourpeople are at the core of our success. Our dedication to fostering an enrichingwork environment is reflected in our recognition as the 'Most PreferredPlace for Women to Work' and as one of the Top 25 Mid-SizedIndias Best Workplaces in Manufacturing for 2025 by GreatPlace to Work. As CMR continues to chart its growth trajectory, we remain committed toinnovation and excellence. We are always looking for enthusiastic and dynamicindividuals to join our team and contribute to our continued success. Position: Plant Head - North(Any plant location in North) Job Band: C Designation: DGM/GM/ AVP/ VP -Plant Operation Reporting to: ChiefOperating Officer Qualification: - Essential B. Tech /B.E inMetallurgy/Mechanical /Electrical Engineering from reputed institute. Desirable Post Graduate Diploma/ Certificate in General Management Experience: Essential -Around 15 + years ofexperience in Plant Operation function preferably in the Metal/ Heavyengineering or Allied industries with minimum 1000 and above workforce. Out ofthem candidate must have exposure of Locations Head at 3 + Yr in large / Mid-Size organization. Desirable - Workingexperience in Global Best -in-class manufacturing practices. Job Profile: Candidate will be responsible forresponsible for complete operations of the business at Unit Level & shalldeliver value in terms of price realization, product efficiency , productivity & quality. Candidate should be High- quality , result Oriented & resilient leader with demonstrated capabilities having techno-commercial acumenfrom the Metal/ Heavy engineering or allied industry., Mainly job involve . Provide inputs to the businessplanning process & determine resource requirements and long-termoperational plans (capacity, lines, expansion, upgradations in line withorganization needs) Provide guidance to variousteams at the plant for achievement of production targets, monitor targetachievement through periodic reviews and any corrective action Guide and ensure coordinationbetween production, quality control, commercial functions and ensure clearunderstanding of targets and expectations Oversee creation of the plantbudget by consolidating inputs from various departments; ensure adherence tothe approved budget. Incumbent will be responsible for Bottom line of theBusiness Monitor adherence to inventorynorms and minimize cost of inventory for all material types (PM, RM & Consumables) Manage the overall IR climate inthe geography and ensure timely awareness and action for managing any peoplerelated issues Undertake discussions withconsultants on project planning, execution of new technology, cost estimationand feasibility study on new projects Oversee adherence to EHS normsand guidelines in all production activity and escalate non-compliance, if any Core Competencies: Stakeholder Management, Hungerto drive transformational changes, Cost consciousness, Effective communication, Execution excellence, Results orientation, Strategic thinking Candidates those profile arematching with our requirement, requested to pls apply. General Age -40- 45 years. CTC 22 to 28 LPA approx. CTCNot a constraint for suitable candidate. Candidate should not be frequentjob changer. Notice Period- Joining periodMax 30 Days. We can buy notice period, if required.

Designation: Tool Room Incharge - Manager/ Deputy Manager / Assistant Manager Total Experience: 15 - 20 Yrs Relevant Experience: 10 to 12 Yrs Educational Qualification: DME/BE - Mechanical or Tool ¨ Location: Karumathampatti, Coimbatore Preferred Companies: Automobile or Engineering Industry Role & responsibilities Ensure Press Tool availbality based on Production Requirment Planning, organize new tool drawing study and planning the new tool as per requirment Ensuring Spare Tool maintenance as per schedule. Ensure Tool Maintenance as per schedule - History card / Repair histroy / Sample inspection / Inspection report. Coordinate with supllier for ontime delivery of new tool as per schedule. Vendor identification and Development QMS and EOHS, customer specific system compliance and Legal compliances Man power allocation and handling. Maintain 5S Leadership & Functional Competencies : People Management, Integrity ,Commitment , Good analytical Skill ,Result Oriented,Communication and Presentation Skill Supervise and Training skill, EOHS, QMS,TPM, 5 S, CNC Knowledge ,New Tool desiging , Procurement. If you are interested, please send your updated CV to this email id sumithra@liderconsulting.com

We are seeking a detail-oriented and proactive Quality Control Engineer with a background in mechanical engineering and experience in fabrication processes. The ideal candidate will be responsible for ensuring that all fabricated components meet the required quality standards, from material inspection through to final product verification. Familiarity with QMS, ERP systems, and fabrication drawings is essential s. Role & responsibilities Understanding fabrication drawing & executing inspection check at different stage. Strong knowledge of light & medium fabrication. Knowledge of Quality process and standards which are followed in Fabrication. Conducting Inward material Inspection and in-house components inspection. Familiar to ERP system & maintaining records in the systems. Maintaining quality document & records for different components. Check & review of Fixture to suit the assembly for fabrication. Knowledge of QMS is necessary. Qualifications Diploma in Mechanical Engineering. Certification of QMS is preferred. NDT level 2 or higher is preferred Experience: 2-4 years in a fabrication or manufacturing quality control role Job location : 832-834, Village Kudali, Taluka Roha, Raigad (MH) 402308, Maharashtra. Type of employment : Permanent. Salary : 3,60,000 ~ 4,80,000 PA. Other benefits EPF, Bonus, Insurance, Gratuity, Paid leaves.... as per company policy.

We are looking for an experienced professional to be the Quality Manager of the NEW Safran Electronics & Defense Indias production site. For the NEW Safran Electronics & Defense Bengalurus production site, and with the support of the corporate team based in Europe, this positions objectives are: 1. Create, Support, Implement and Manage the new site Quality Management System to be compliant with the latest version of ISO9001 and AS9100s requirements. 2. Build and hire the local Quality team that will support and maintain the local Quality Management System. 3. Create, Support, Implement and Manage all the Quality methodologies and tools to ensure the quality performance monitoring through relevant KPIs such as but not limited to On Time Delivery and Product Quality. Complementary Description KEY RESPONSIBILITIES 1. Site Quality referent for all Quality topics (Certifications, Quality in Production, Supplier Quality, Metrology, etc.) o Assures quality products and processes by establishing and enforcing quality standards o Responsible for the development, and implementation of complete QA to support multiple product lines and services while ensuring agreement with stakeholders o Responsible for establishing quality objectives for multiple products/projects ensuring they meet the quality standards and the Safran Group procedures & guidelines o Ensure that there is a Risk Management methodology applied and prioritise accordingly o Support and train the Quality team on methods and tools related to Quality 2. Focal point for the Quality topics to communicate with the SED Quality TOP management team. o Brainstorm and interact with SED/Safran India and France to get support and/or guidelines to build the local SED India QMS o Provides oversights and inputs to all aspects of quality management and assurance 3. Quality referent on all the Quality topics during all industrial transfers phases to ensure that the procedures and other supporting documentation in the QMS are complete and accurate with the local environment and activities. Job Requirements More than 5 year experience in the industrial environment ( aerospace or electronics production preferable ) Good knowledge on Quality Tools ( 8D/ FMEA / Risk Management / QRQC ) and or on specific aviation legislation ( PART21G / PART145 ) will be beneficial but not mandatory

Position Title Manager / Deputy Manager - Plant Maintenance Preferred Companies - Automobile or Engineering Industry Location - Karumathampatti, Coimbatore Key Responsibility Maintenance of Air Compressors, , ETP, STP, Pollution control & Fire Hydrant system, Gas Plant, Buildings, Solar panel, Pressure Stove ,Chiller and Air Conditioning System .... Planning, organize spares & other resources for effective & economical manufacturing. Ensuring adherence to Preventive Maintenance schedule. Ensuring the basic condition of Plant & Machines. Ensuring maximum uptime of Plant machineries. QMS and EOHS, customer specific system compliance and Legal compliances Man power allocation and handling. Maintain 5S Knowledge , Skill and Experience : Educational Qualification DME/BE - Electrical with C License Soft Skills SAP and MS office Total Experience 15 to 20 Years Leadership & Functional Competencies : People Management, Integrity ,Commitment , Good analytical Skill ,Result Oriented, Communication and Presentation Skills,Supervise and Training skill, EOHS, QMS,Utilitity Maintenance Knowledge, TPM, 5 S, Genset, Transformer, Compressers,Solar Energy.. . Interested Please call Mithra-HR 9176616016

ASTER DM HEALTHCARE LIMITED is looking for Manager Quality Management to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes Apply subject expertise to support operations, planning, and decision-making Utilize tools, analytics, or platforms relevant to the job domain Ensure compliance with policies while improving efficiency and outcomes