433 Capa Jobs - Page 11

We are currently looking for a Head Logistics Engineering to join our client (a leading asset pooling company) in Mumbai. This is a critical leadership role within our Solutions Design team, focusing on logistics, transport, and packaging solutions. Key Requirements: Minimum 15 years of experience in the packaging industry (FMCG, Pharma, Beverages preferred). Strong expertise in packaging materials (Primary, Secondary, Tertiary) and customized automotive packaging . Hands-on experience in project management, supplier relations, and process compliance . Knowledge of AQL Inspection, Testing, 5S, QC Tools, CAPA, Kaizen, and SOP preparation . Familiarity with 3D and 2D packaging design and Microsoft Project Software is an added advantage. Age: Ideally between 30-35 years . Preferably from IIPM or similar background working in companies using plastic-based packaging, a person reporting to the Packaging Head. CTC: Upto 45 lakhs+ (80 % fixed, 10 % variable, 10% long term incentives), additionally ESOPs may also be offered.

Role & responsibilities Description of duties & activities Product Quality Assurance through Process Control & Compliance During Production : 1. Receiving Inspection of Critical Components against Specification 2. Auditing of critical process control parameters & timely escalation of deviation cases for CAPA 3. Define quality screening parameters / test methods & sampling plan at appropriate production stages Monitor fallout at each screening stations- initiate improvement actions to control the same Prepare & Share quality KPI reports for MIS Product Performance & Reliability Testing 1. Prepare, execute product performance & reliability test plan 2. Ensure compliance to specification 3. Initiate CAPA in case of deviation People Management: 1. Lead, support & manage team of technicians 2. Train people with new / additional skill sets Support New Product Release 1. Review & revise quality check points / test methods & equipments 2. Coordinate to Prepare & execute Qualification plan 3. Gate keeper for all new product release projects. Product / Process Certification (UL/CCC/ISI) 1. Ensure product compliance to requirements 2. Inclusion of new product in certification list Preferred candidate profile Bachelors in mechanical/Production Engineering,. 2-4 years Experience of Working in Quality / Mfg function Perks and benefits PF, Mediclaim, Transport, Canteen Note: This position is on third party Payroll

About The Role Key Responsibilities Asset Inventory and Data Management Maintaining accurate records of all hardware and software assets; including details like purchase date; serial numbers; license information; and current status. Implementing and managing an asset management system to track asset lifecycle stages (acquisition; deployment; maintenance; disposal). Data cleansing and validation to ensure data integrity within the asset management system. Compliance and Risk Management Monitoring software license compliance to prevent potential vendor audits and legal issues. Implementing and enforcing asset management policies and procedures to mitigate risks associated with asset usage and disposal. Conducting regular asset audits to identify discrepancies and address compliance concerns. Strategic Planning and Optimization Collaborating with stakeholders to develop an overall asset management strategy aligned with business objectives. Analyzing asset usage data to identify opportunities for cost reduction and asset optimization. Forecasting future asset needs based on business growth and technology trends. Vendor Management Negotiating contracts with software and hardware vendors to ensure favorable pricing and licensing terms. Managing relationships with vendors to address asset-related issues and ensure timely support.

- Must have good knowledge of Regulatory Submissions and Research - Must be familiarity with chemical industry specific regulations and guidelines. - Prepare and submit regulatory documents, such as INDs, NDAs, and MAAs, to regulatory agencies Required Candidate profile - Ensure company products with relevant regulatory requirements such as USFDA, FDA, EMA, and local regulations. - Stay up-to-date with changing regulatory requirement to internal stakeholders.

Role & responsibilities Customer complaint handling- MSIL, HCIL, HMSI, IYM, SMIPL Customer complaint analysis & CAPA Injection moulding process know how Warranty part analysis SPC MSA QC Tools 2D drawings, GD&T CARV/GIPP/IPP ECN/DCN Preferred candidate profile Customer specific requirement Customer complaint handling- MSIL, HCIL, HMSI, IYM, SMIPL Customer complaint analysis & CAPA Perks and benefits

Handle Overall Plant. Coordinate production, maintenance, shipping & quality control activities in a factory or other manufacturing plant. Overall knowledge of CNC/VMC/HMC Machines. Must be have experience Automotive Machining Background. Required Candidate profile Proficiency in CNC programming languages & CAD/CAM software CAPA, 8D Problem solving technique. Awareness about Cutting tools & their Life monitoring, Automation & Robotic concept

Knowledge of Measurement Instruments/ Gauge/ Tools/Fixtures * Knowledge of Calibration Reports * Knowledge of CAPA Report * Prepare Supplier Audit plan & Audit report * Knowledge of SPC report, MSA inspection & Layout Inspection Reports Required Candidate profile 6- days working Knowledge of Computer (Ms-Office/Ms Excel/ Ms Powerpoint)* • Knowledge of English* * Knowledge of Reading Mechanical Drawings

JD: 1) To be prepared document related to audit as per audit agenda. 2) Filled vendor questionnaires & prepared related documents. 3) Keeping record of key Customer. 4) To be prepared process validation protocol and report as per seniors guidance. 5) To be prepare cleaning validation protocol and report as per seniors guidance. 7) To be prepared master, controlled, uncontrolled, reference, obsolete & distribute documents as per SOPs and formats requirement. 8) To help the senior for preparation of CAPA according to audit report. 9) Issuance of Change control, OOS, deviation & other QMS formats whenever required from respective department and retained record in logbook. 10) To be prepared BPCR as per procedure. 11) To be issue BPCR to all blocks as per prerequisite. 14) To be handle change control, market complaint, deviations, CAPA. 15) To be issue documents, protocols, log book and format to all department as per prerequisite. 16) Retrieval of documents. 17) To be controlled all master documents. 18) To be prepared schedule & conduct Internal audit. 19) To be prepared APQR of all products. 20) Preparation of documents for Certification & product registrations work i.e. FDA, Halal, Kosher, Reach. etc. Review specification, test procedure and SOP's for their deficiencies according to audit points 1) To be prepared document related to audit as per audit agenda. 2) Filled vendor questionnaires & prepared related documents. 3) Keeping record of key Customer. 4) To be prepared process validation protocol and report as per senior’s guidance. 5) To be prepare cleaning validation protocol and report as per senior’s guidance. 6) To be conduct training and evaluation done as per Schedule. 7) To be prepared master, controlled, uncontrolled, reference, obsolete & distribute documents as per SOPs and formats requirement. 8) To help the senior for preparation of CAPA according to audit report. 9) Issuance of Change control, OOS, deviation & other QMS formats whenever required from respective department and retained record in logbook. 10) To be prepared BPCR as per procedure. 11) To be issue BPCR to all blocks as per prerequisite. 13) To be prepared data for monthly report as per QMS and submit to senior. 14) To be handle change control, market complaint, deviations, CAPA. 15) To be issue documents, protocols, log book and format to all department as per prerequisite. 16) Retrieval of documents. 18) To be prepared schedule & conduct Internal audit. 19) To be prepared APQR of all products.

Role & responsibilities 1. Shall have an exposure to SRA inspections like USFDA, EU, TGA etc. 2. Should have experience of implementation and handling and troubleshooting any of QAMS software like Trackwise /calibre(DMS, QMS), nichleone(TMS), LIMS,SAP etc. 3. Should have experience of handling QAMS notifications like change control, deviation, OOS, incidents, risk assessment, market complaint, etc. 4. Should have an experience of MRM/ IPQA / participation in internal. Preferred candidate profile B. Pharm/M. Pharm with 4+yrs of experience in implementation of QAMS software, LIMS, SAP, nichleone.

Responsible for coordinating investigation of deviations, out of specifications, complaints, technical report writing on investigations, track CAPA implementation Responsible for logging and coordinating investigation of IPQA observations, deviations, OOS, OOTs, Complaints Compilation of investigation details and Technical Report writing for failure investigations. Logging CAPAs and Tracking implementation of CAPA Presenting and explaining failure investigations to regulatory auditors, customer auditors

Role & responsibilities Check all SOPs of QC available Check the record of cleanliness of the area. Check the list of instrument/equipment update Check that activities like sampling, testing and handling of special chemicals are done by taking proper precautions. Check that labeling are done on samples withdrawn and after passing. Check standardization of reagent/solution and labeling. Check whether signed specification and method of analysis are available. Check the calibration record of instrument/equipment. Check the calibration chart for all instrument/equipment. Check all the analyst qualified and record available. Check the stability sample against stability schedule. Check the stability record against stability program. Check whether water sampling is done as per sampling plan. Check the analysis record of water for chemical and microbial tests. Check the record of standardization of volumetric solution. Check the sample entry register and ensure sampling is done as per sampling plan. Check any analysis record to ensure that analysis is done as per specification and test procedures are strictly followed. Check approved vendor list available and updated. Check number of out of specification since last audit. Check and issue of BMR/BPR. Check the medical examination report. Check the record for cleaning of water tank. Check entry and exit of personnels and visitors record. Check and keep pest control record. Taking approval for new product and made necessary document. Keep track on training record (in house /external). Vendor audits Keep the record of hazardous material. Prepare new BMR for new product. Keep the inventory for glassware and chemicals. Keep the record for finished goods. Check the storage condition for raw materials and finished goods. Keep the record of stereo control. Check the status labeling. Keep the log book for instrument. Area monitoring and pressure differentials. Monitoring of quality of water. Maintain the record of preventive maintenance. Keep the record of calibration and validation method. Keep the record of stability studies, Change control, Deviation, MFR’s. Maintenance of working standards. Records of control sample. As on when Management Assigned any Job. Dispensing/checking of dispensed RM/PM. Process validation. Regulatory affairs. Preparation of SOPs QC related routine activities(periodic checking of QC reports and records) MFR writing and BMR management. Documentation control. Complaint handling. Face FDA inspection, ISO audit, outside party inspection. Face Internal audit. Worked as chemist in QC lab handling all day-to-day work. Familiar with IP BP & USP Methods of analysis. Analysis of raw material & finished products having experience in good laboratory practices. Made GLP By control Charts & In House QC samples & Standards Participated in round robin analysis with different laboratories like shell & sabic Familiar With ASTM, UOP & IP methods of testing Actively Participated in Interview Recruitment of new Chemist Having excellent safety and attendance record. Authorized For IATA to sent samples & Dangerous Goods by air Made Laboratory Hygiene plan & Quality Check Plan Review and approval of Laboratory investigations. Review and approval of investigations related to deviation and market complaint. Review and approval of CAPA proposals. Review and approval of change controls. Evaluating trends of Deviations, Complaints and OOS, proposing CAPAs based on evaluation and assuring implementation of the same. Participation in Regulatory inspections, compiling inspectional responses and monitoring compliance. Annual product quality review. Vendor Management Conducting internal audits. Conducting weekly meetings of Quality functions. Participating in Management Review Meets. Conducting training on ‘QMS related procedures’, ‘Conduct during inspections’, ‘Effective review practices’, ‘Data integrity’ etc. Review of change controls, investigation of Deviation & Laboratory Investigations. Investigations of market complaints, Root cause analysis & implementation of CAPA. Evaluating trends of Deviations, Complaints and OOS, proposing CAPAs based on evaluation and assuring implementation of the same. Preparation & revision of Site master File, Validation Master Plan and QMS SOPs. Preparation for Regulatory inspections, compiling inspectional responses and monitoring compliance. Communication with clients related to investigations/ inspectional compliance. CAPA effectiveness verification. Review and monitoring of cleaning validation program. Participating in self-inspection program. Preparation & Participating in Management Review Meets. Review of risk assessment of various functions. Conducting training on ‘cGMP’, ‘QMS related procedures’, etc. Monthly Auditor for lab Preferred candidate profile Perks and benefits

Role & responsibilities :- Lead the development, implementation, and continuous improvement of our Quality Management System (QMS). Ensure adherence to industry standards and regulatory requirements (e.g., EMA, WHO). Collaborate with cross-functional teams to drive quality initiatives and foster a culture of quality. Oversee audits and inspections, ensuring timely resolution of findings and implementation of corrective actions. Analyze quality metrics to identify trends and recommend improvements to enhance product quality and safety. Develop and implement quality management system policies and procedures. Identify, analyze, document and report on system deficiencies. Monitor and evaluate the effectiveness of the quality management system. Ensure compliance with applicable standards and regulations Train employees on quality management system procedures and processes Perform internal audits and lead external audit activities Develop and maintain quality management system documentation. Manage and investigate customer complaints Analyze data and produce reports to present to management. Monitor performance and implement corrective action plans.

Quality Strategy and Planning: Develop and implement quality strategies and plans to ensure that products meet customer requirements and industry standards. Quality Policy and Procedures : Develop, implement, and maintain quality policies and procedures to ensure compliance with regulatory requirements and industry standards. Quality Assurance and Control: Ensure that quality assurance and control processes are in place to prevent defects and ensure that products meet quality standards. Audits and Inspections: Conduct internal audits and inspections to ensure compliance with quality policies and procedures. Corrective and Preventive Action : Identify and implement corrective and preventive actions to address quality issues and prevent recurrence. Supplier Quality Management: Ensure that suppliers meet quality standards and requirements Customer Complaints and Feedback: Investigate and resolve customer complaints and feedback to ensure that quality issues are addressed. Quality Metrics and Reporting: Develop and track quality metrics and reports to measure quality performance and identify areas for improvement. Team Management: Lead and manage the quality team to ensure that quality objectives are met.

Documentation, compliance, and regulatory audits, analytical testing, formulation development and process optimization, microbial testing and sterility assurance, ensuring adherence to GMP, GLP, & ISO, managing deviations, CAPA, maintaining QMS & RC Office cab/shuttle Food allowance Annual bonus Provident fund House rent allowance Over time allowance Employees' state insurance

Responsibility includes: Develops quality assurance plans by conducting day-to-day analyses Determining the quality assurance requirements which will insure compliance of in-process and final production are in compliance with company and customer quality standards and delivery requirements Ensuring adherence to ISO regulations other Industry requirements and Government regulations Determine manufacturing impact of quality specifications, drawings, and purchase orders Evaluates customer contractual specifications, and determines and implements Quality Assurance requirements specified by customer contract Acts as a liaison and as a technical resource internally to support areas such as Program Management, Manufacturing Supervision and Quality Engineering in analysis and resolution of production issues Provides quality and inspections sign-off and approval for all production Responsible for assuring that the Quality Manual, Quality Procedures, Work Instructions and all other Quality forms and documentation are maintained current and are being accurately implemented by applicable departments Monitor and facilitate adherence to IS & ISO with proven experience in product quality, quality management, floor management, production cycle, 5S implementation, KAIZEN, customer requirements & other regulator and customer driven quality systems Directs the external audit of the Quality Management System for compliance to established customer requirements Experience required: Proven influencing skills to achieve results and maintain positive 360 degree working relationships, particularly one must effectively influence peers or those with more senior roles Strong organization, time management, and communication skills essential Experience as a key contributor cross functional teams, serving as a key representative for a given function / area Exposure to technical aspects of the role including technical writing, systems testing, quality and compliance Prior direct supervision of teams Experience with testing frameworks including sampling methodologies, data analysis, and reporting Diploma, B Tech, BE -Electrical/Mechanical, proficient in MS Office

Leading BPO in Gurgaon & Bangalore Hiring for Transactional Quality Manager International Voice Process Must be a Manager Quality On papers in an International BPO in Voice process Over All Experience 8+ Years CTC UPTO 16LPA based on Last CTC & experience Interested candidates can mail their cv at simmi@hiresquad.in or call at 8467054123 Role & responsibilities Act as a primary POC between the QA teams, OPS & clients. • Recommended responsibilities include but are not limited to the following: • Lead, manage, motivate, and mentor a team of Quality Analysts • Drive consistency to ensure the strong quality performance and alignment across all programs • Deliver process as well as agent level insights to continuously improve and deliver outstanding customer experience across the program • Work alongside Ops and hiring team to provide on-boarding, coaching, remediation, training and development for QAs and QA Leads • Implement and drive the QA process and structure • Identify possible issues and trends and give actionable insights while communicating them to relevant stakeholders • Implement initiatives and projects to counteract any possible trends, drive business KPIs • Aggregate audit findings and analyses gaps in processes, identifying innovative ways to solve problems upstream, help improve customer experience and drive higher efficiency • Analyses quality and performance trends to provide recommendations for program improvement • Responsible for the delivery of vendor quality metrics at management reviews Key skills & knowledge: Excellent communication & interpersonal skills Excellent MS Office skills (presentation & excel) Should have good knowledge of FMEA identification and mitigation of vulnerabilities Excellent knowledge of Quality & Analytical tools Should be well versed with Qualitative concepts Should have worked on process improvement projects driving Customer Experience, Process Improvements & Profitability Interested candidates can mail their cv at simmi@hiresquad.in or call at 8467054123

Role & responsibilities Prepare and Review SOPs and Guideline for DQA. Formulate Documentation Process for the Key divisions of SRD and ARD. Review documents with respect to drug substance such as protocols, SOPs, test methods, data COAs and report through collaborate with CRD, ARD, and QC scientists. Successfully manage and complete all Audits that come up from time to time and conduct periodic internal audits and ensure compliance as per regulatory requirements Review process development documents including KSM/KRM identification, specification proposal, analytical method development and validation reports, stability protocols& reports and safety studies. Handle Vendor Qualifications for KSM/KRM, Solvents etc. Ensure Regulatory compliance as per USFDA and other such regulatory bodies. Support and handle all aspects pertaining to new product development patent filing, license approvals etc Impart training to all employees on SOPs/Safety. Support on Onboarding on new employees joining the organization Responsible for assessing the impact, review and closure of change control requests and deviations. Responsible for CAPA implementations, verifications of and effectiveness. Preferred candidate profile Bachelors or Masters degree in Pharmaceutical Sciences, Chemistry, or related field. Minimum 5-8 years of experience in Quality Assurance, with at least 2 years in a supervisory role in the pharmaceutical industry, specifically with API products. In-depth knowledge of GMP, ICH guidelines, FDA, EMA regulations, and quality systems. Proven experience in conducting internal and external audits, and leading regulatory inspections. Strong understanding of the API development and manufacturing process. Ability to manage cross-functional teams and interact with senior management

Responsible for Effectiveness and efficiency of quality function in Oil and Gas ( from Inward to Customer feedback). Responsible for implementation and adherence of Quality system. Ensure effective Quality planning at all stages; Incoming, In process, Final. Ensure required inspection instruments are available duly calibrated. Ensure effective in process inspection like set up approval and in process audit inspection to detect the in-process NC if any. Attend NC at this stage and initiate CAPA to ensure quality at this stage. Ensure timely completion of final inspection. Ensure timely incoming inspection and feedback to respective stakeholders. Monitor final inspection and incoming inspection, mobilize required resources as per priority whenever required. Responsible for root cause analysis and Implement effective CAPA mechanism (for customer complaint and repetitive internal rejections) Responsible for handling customer inspection. Drive efficiency in overall inspection activity. Responsible for performance evaluation of quality team and impart training whenever required. Ensure effective program control of CMM programs. Ensure all ERP system related entries on time, accurate for Quality department. Ensure all Portal entries on time, accurate for Quality department. Responsible for preparing Quality department related MRM data and should be made available whenever required. Ensure All Quality records for dispatched parts are stored and retained as per requirement and will be made available whenever required. Responsible for continuously upgrading inspection methods by using the latest technology to make it more cost effective. Single point contact for all quality related communication to customer Perform other duties as directed by superiors. Maintaining 5s at work area.

Handling of Equipment Qualification, Area Validation, Process validation, cleaning validation, Risk assessment, Change control, Deviation, HVAC validation please share your profile & contact: Call: 8160615349/7878051751

Role: GRC Manager Location: Gurugram Mode: Work from office in sector 22 Gurugram Preferred candidate profile Functional Knowledge : Experience of working in InfoSec/Compliance team/Risk & Compliance team & managing client/internal/external audits Experience of audit/implementation of ISO 27001/PCIDSS etc Experience in Risk & Compliance Role & Responsibilities: Responsible for driving the security policies across organization Conducting audits and releasing reports to stakeholders Assist stakeholders on CAPA for audit findings and tracking of closures Assisting in internal & external IT/Infosec audits (e.g. ISO 27001, PCIDSS, SOC reports etc.) It is our policy to provide equal employment opportunities to all individuals based on job-related qualifications and ability to perform a job, without regard to age, gender, gender identity, sexual orientation, race, color, religion, creed, national origin, disability, genetic information, veteran status, citizenship or marital status, and to maintain a non-discriminatory environment free from intimidation, harassment or bias based upon these grounds.

Designation: Quality Assurance Chemist Location :Medchal, Hyderabad Qualification: B.sc/B.pharma Experience: Min.3 relevant exp as Qa chemist Package: 4-5LPA Shifts: General shifts If interested Contact: 8247381453 Share Cv laxmi@hireiton.com Required Candidate profile • Qualification of utilities like Purified Water systems • Reviewing BMR/BPR & issuing analytical worksheets, logbooks • Must have worked in a pharmaceutical company in the past

Job Description: 1. Will be responsible for managing the QA Dept & Performing in process checks as per SOP. 2. Preparation & Execution of SOP 3. Investigation of root cause & implementation of CAPA, Handling deviations, Non-Confirmities, OOS, CC, CAPA Tracking 4. Manage day to day activity 5. To maintain all calibration records & its corresponding documents 6. To schedule

JOB DESCRIPTION 1) ARD Scientist (Analytical Research & Development Scientist) Positions Sr Scientist -1 Junior Scientist-2 Job Description: ARD Sr Scientist/Jr Scientist capable in developing and validating analytical methods and Validation including calibration to ensure the quality and stability of pharmaceutical products. Key Responsibilities: Develop and validate analytical methods for drug substances and drug products. Perform analytical testing such as HPLC, GC, and wet analysis. Interpret analytical data to assess product quality, purity, and stability. Implement GLP & GDP practices. Prepare technical reports and documentation for regulatory submissions. Collaborate with the FRD & DQA to support product development. Troubleshoot analytical method issues and recommend improvements. Qualifications: Masters degree or Ph.D. in instrumental analysis, Analytical Chemistry, or related discipline. Expertise in analytical techniques such as HPLC, GC, and spectroscopy. Strong knowledge of regulatory guidelines such as ICH and FDA. Good documentation and report-writing skills. Problem-solving and analytical thinking abilities. Minimum 3(or) More Years for Junior scientist of experience in ARD /Q.C . For Sr Scientist 8 (or) more years of experience is desired 2) FRD Scientist (Formulation Research & Development Scientist) Positions Sr Scientist -1 Junior Scientist-2 Job Description: FRD Sr Scientist/Jr Scientist is responsible for the research and development of pharmaceutical formulations, ensuring the products are safe, stable, and effective for consumption. Key Responsibilities: Design, develop, and optimize formulations for pharmaceutical or nutraceuticals Etc. Implementation of QbD . Conduct experiments to test product stability, and efficacy. Prepare technical documents, including formulation protocols and reports. Collaborate with cross-functional teams such ARD, DQA Etc to ensure compliance. Troubleshoot formulation issues and propose solutions. Qualifications: Masters degree in pharmaceutics or Ph.D. in Pharmaceutics & Equivalence, Minimum 3(or) More Years for Junior scientist of experience in FRD /R&D . For Sr Scientist 8 (or) more years of experience is desired Strong understanding of Good Manufacturing Practices (cGMP). Problem-solving skills and GDP implementation Skills in usage of software for developing of formulation and characterization. Excellent communication skills to present findings and collaborate with teams. Exposure in developing Liquid Orals, Solid Orals, Semi-Solid Orals. Nano formulations will be preferred 3) DQA Team (Development Quality Assurance Sr. Executive) Positions Sr Executive -1 Jr Executive -1 job Description: DQA Sr. Executive should monitor the quality assurance processes during product development, ensuring that all stages comply with quality standards and regulatory requirements and product specification need as per ICH Guidelines. Key Responsibilities: Lead quality assurance activities for product development, including design, testing, and validation stages. Ensure compliance with regulatory guidelines and quality standards (e.g., FDA, EMA, GMP). Develop and implement quality control procedures for new product development. Conduct internal audits and prepare quality assurance reports. Collaborate with R&D, ARD to implement the quality issues. Manage risk assessment processes and ensure continuous improvement in quality systems. Should have knowledge in QbD system for product development. Qualifications: Minimum experience should be 6-8 Years for sr executive and 1 to 3 years for junior executive in DQA (or) Q.A Bachelors or Masters degree in Quality Assurance /Analysis/Pharmaceutics, In-depth knowledge of cGMP, GDP, GLP, ICH and regulatory requirements and implementation. Excellent communication and problem-solving skills.

Role - CSV Consultant Exp - 4+ Years Skills - CVS , CAPA, Gamp, Gxp, SAP / LIMS / LABWARE Permanent: Harjai Computers Pvt.LTD Location: Mumbai Work location - WFO Mode of working- 5 days, Monday to Friday Interview Mode - VC round

Requirements : Qualification: Diploma ((Mechanical Engineering / Industrial Engineering) and / or B.E. (Mechanical Engineering / Industrial Engineering/Production Engineering) Interest in Quality Assurance and Control in a Fabrication & Manufacturing unit, and spending time on the shop floor and conducting the inspections personally Minimum Experience : 2~4 Years in welding and painting inspections for Metal Fabricated components / Heavy Fabrication industry. People from experience solely from auto components industry are not preferred. Knowledge of Non-destructive testing, WPS/PQR/WPQ, reading and assessing material TCs, QAP/ITP. Candidates with NDT Certification (Level 2) for LPT/VT/UT/RT will be preferred. Knowledge of ISO 9001 (QMS). Self motivated & confident, Pro-active, Enthusiastic & energetic, Able to work independently with minimal supervision Basic proficiency in writing grammatically correct emails and spoken (telephonic English) * Previous experience in similar field (Industrial Noise Control) will be preferred. Duties & Responsibilities : Quality Assurance & Control Conducting thorough quality checks at every stage, including material receipt, during production stage inspections, and after assembly before dispatch for all projects and creating quality records and reports. Ensuring recording and reporting all the Non-conformances in the project and ensuring RCA and CAPA is provided by the production team to close the NCs. Taking ownership of quality departmental objectives and planning execution of the same. Performing Internal Inspections (Product, Plant, etc.) & coordinating Customer Inspections, Audits, etc. and Striving to achieve Zero Defects, First Time Right and 100% Successful Customer Inspections for all projects. Ensuring maintenance and calibration of all the equipment and reporting all non-conformances and non-performances of equipment. Processes & Systems: Assisting the Project Manager in documentation for ISO 9001 (Quality Management System), ISO 14001:2015 (Environment Management System), ISO 45001:2018 (Occupational Health & Safety Management System), EN1090, ISO 3834 and other audits Other Details : Remuneration : Salary: Total Annual CTC (Fixed + Variable): INR 4,00,000 to INR 5,25,000 Office Timings : Monday - Saturday : 9:00 AM to 6:00 PM Location : ARK Corporate Office, S-181 MIDC Bhosari, Pune 411026, MH, India Positions open : 1