Quality Assurance Executive Jobs in India

We are looking for a dedicated Quality Assurance Executive to ensure that our products meet the highest quality standards. You will be responsible for monitoring the production process and performing quality checks to identify and resolve any issues.**Key Responsibilities:**- **Conduct Quality Inspections:** Regularly inspect products during and after the production process to ensure they meet our quality specifications.- **Documentation:** Maintain accurate records of quality tests, inspections, and any non-conformance issues to help track improvements and trends.- **Develop Quality Standards:** Collaborate with the production team to establish and update quality standards and procedures to enhance product quality.- **Train Team Members:** Provide training and guidance to staff about quality assurance processes and procedures to promote adherence to quality standards.- **Report Findings:** Prepare reports on quality issues, trends, and improvement areas and communicate these findings to management and relevant teams.- **Implement Improvement Strategies:** Work with various departments to develop strategies for reducing defects and improving overall product quality.**Required Skills and Expectations:**Candidates must have a diploma and between 2 to 5 years of experience in quality assurance. You should possess strong attention to detail and analytical skills to identify quality issues. Excellent communication skills are vital for effectively conveying quality standards and metrics. Proficiency in quality management tools and methodologies is preferred. You should be a team player who is adaptable and committed to maintaining high quality in all processes.

Role & responsibilitiesQA DocumentationPreparation, review, control, and archival of SOPs, STPs, GTPs, Specifications, and Protocols.Ensure compliance of documentation with cGMP, GLP, and regulatory requirements.Handling of document control system including issuance, reconciliation, and retrieval.Support audit readiness by maintaining updated quality documents.Review of analytical reports, logbooks, and batch-related records.QA Validation & QualificationExecution of Equipment Qualification (IQ/OQ/PQ) for analytical instruments.Preparation and review of validation protocols and reports for process and analytical methods.Cleaning validation and utility qualification support.Preparation of Validation Master Plan (VMP).Coordination with QC and Engineering teams for validation activities as per regulatory guidelines.Quality Management System (QMS)Handling of deviations, CAPA, Change Control, OOS, and OOT investigations.Conduct internal audits and ensure compliance with QMS requirements.Risk assessment and root cause analysis for quality incidents.Monitoring and trending of quality metrics.Preparation and review of quality reports and audit documentation.IPQA (In-Process Quality Assurance)Line clearance and in-process checks during analytical and lab activities.Monitoring of sample handling, testing procedures, and documentation practices.Verification of compliance to SOPs and regulatory guidelines during operations.Review of batch records and analytical test data.Ensuring adherence to Good Laboratory Practices (GLP).QC InstrumentationOperation, calibration, and maintenance of analytical instruments such as HPLC, GC, UV, FTIR, etc.Execution of analytical method validation and instrument qualification.Preparation of calibration and maintenance records.Troubleshooting of instruments and ensuring uptime.Compliance with data integrity and regulatory standards.QC MicrobiologyEnvironmental monitoring and microbial testing.Sterility testing, MLT, BET, and water analysis.Media preparation and growth promotion testing.Handling of microbial cultures and documentation.Ensuring GLP compliance in microbiology laboratory operations.Preferred candidate profileBachelors / Masters Degree in Pharmacy, Microbiology, Biotechnology, Chemistry28 years of experience in QA/QC within a Pharma industrySound knowledge of cGMP, GLP, Data Integrity, and regulatory requirements.

Designation :- Quality AssuranceQualification:- D.Pharma/B.PharmaExperience :- Fresher Salary:- As Per Interview Gender:- MaleJob Location:- Boisar, Maharashtra Industry:- Manufacturing Industry/Reputed Engineer Company

We are looking for a detail-oriented Quality Assurance (QA) Executive to monitor and evaluate processes, documentation, and service quality across our operations. This is a non-technical QA role, ideal for candidates with strong observational, communication, and documentation skills.Key Responsibilities:Conduct routine checks and audits of processes and documentationIdentify gaps in SOP (Standard Operating Procedure) adherenceMaintain quality records and audit reportsCoordinate with internal teams to resolve quality issuesEnsure compliance with company standards, regulations, and guidelinesParticipate in process improvement initiativesSupport training and onboarding processes with quality inputsProvide timely feedback and reporting to QA Manager or Team Lead

Develop and Implement Quality Standards: Create and enforce quality assurance protocols, standards, and procedures to ensure all products or services meet internal and external benchmarks.Conduct Audits and Inspections: Regularly perform audits and inspections on products, processes, and systems to identify defects, deviations, or areas for improvement. This includes raw materials, in-process goods, and final products.Monitor and Analyze Quality Metrics: Track and analyze key quality metrics, such as defect rates, customer complaints, and rework costs. Use this data to identify trends, diagnose root causes of issues, and develop corrective and preventive action plans.Documentation and Reporting: Maintain detailed and accurate quality records, including test plans, inspection reports, and defect tracking logs. Prepare and present reports on quality performance to senior management.Collaboration and Training: Work closely with production, engineering, and supply chain teams to integrate quality standards into daily operations. Provide training and guidance to employees on quality procedures and best practices.Ensure Compliance: Stay up-to-date with relevant industry regulations and certifications (e.g., ISO 9001, GMP) and ensure all processes and products are compliant.

Job Profile of Quality Assurance Manager Qualification -Graduate /Diploma engineer Work experience- with 5-8 years hands on experience in handling Quality Assurance of EPDM extrusion/Parts or Engineering components in an automobile company/ancillary Should be well versed with IATF 16949:2016 system implementation and maintenance of system Hands on experience in process control activities Should be able to maintain discipline on the shop floor. Hands on experience in root cause analysis and taking corrective action and leading the CFT team Good communication skill, should feel at ease in communicating with the customer Will be responsible for maintaining Zero defect supplies to customers. Will be responsible for implementation and maintenance of 5 S activities Will be responsible for daily report analysis, corrective actions and Quality MIS to management Should have hands on experience in controlling the external and internal PPM by taking effective corrective action and monitoring of the same Should have leadership qualities and be able to build team Should have process-oriented approach and be able to improve /help improve process capabilities Should be well versed with automobile OEMs system requirement and approach.

Key Responsibilities: Ensure medical devices comply with all applicable national and international regulatory requirements and standards Prepare and submit regulatory submissions, including 510(k), PMA, and other global market registrations Communicate with regulatory authorities (such as the FDA, CDSCO) to handle queries and support approval processes Monitor and interpret changes in medical device regulations and assess their impact on the company Provide regulatory guidance and training to cross-functional teams including R&D, QA/RA, and Product Development Develop and implement regulatory strategies to support new product development and market expansion Maintain organized, up-to-date documentation to demonstrate compliance and support audits Collaborate with channel partners and internal documentation specialists to ensure consistent regulatory alignment________________________________________Requirements: Bachelors degree in Biomedical Engineering, or B.E electronic commination. or a related discipline 3 - 4 years of experience in medical device regulatory affairs Strong knowledge of domestic and international medical device regulations (FDA, EU MDR, ISO 13485, CDSCO, etc.) Excellent verbal and written communication skills High attention to detail, analytical thinking, and problem-solving ability Experience working collaboratively across multiple tea

In the paper industry, Quality Assurance (QA) plays a crucial role in ensuring consistent product quality, meeting customer requirements, and complying with industry standards. QA focuses on preventing defects and refining manufacturing procedures throughout the production process.Job Description:Quality Control: Involves regular checks and measurements during production to ensure products meet specified qualities, often incorporating Total Quality Management (TQM).Testing and Measurement: Utilizes various testing instruments and methods to assess physical and chemical properties of paper and its products, including thickness, density, tear strength, and burst strength.Process Control: Involves monitoring and adjusting various parameters during the papermaking process to maintain consistency and optimize performance.Raw Material Inspection: Ensuring the quality of raw materials like pulp, fibers, and chemicals used in paper production.Continuous Improvement: Regularly reviewing and improving QA procedures to enhance product quality, reduce waste, and optimize operational efficiency.Compliance with Standards: Adhering to industry standards and regulations, such as ISO 9001:2000, to ensure quality and safety.Data Analysis and Management: Utilizing data from online systems and web inspection systems to analyze roll quality and identify areas for improvement.Preferred ExperienceCandidates with experience in the following industries will have an added advantage:Paper Mills and Paper ConversionFood PackagingWhy Join Nationwide Paper Ltd?Be part of a global leader in sustainable packaging solutions.Opportunity to work in a fast-paced and innovation-driven environment.Professional growth opportunities and competitive compensation.

Job Description:1) Closely communicate with the Inspection Coordinators to schedule the inspection assigned.2) Implement inspection according to operation guidelines, inspection guidelines, and any special instructions provided by the company.3) Complete the inspection report with photos and submit it to Technical Manager within the required time limit.4) Submit the inspectors job expense claim form and reimbursement documents monthly and meet financial requirements.5) Perform other duties and responsibilities as assigned by supervisor/management.Requirements:- College graduate or above.- Major in Engineering (Textile, Furniture, Mechanical, Electronic, etc.)- Having more than 1 year more working experience in the inspection field or quality control background of products of Softlinesor Hardlines.- Familiar with the AQL standard and good knowledge of safety and regulation standards.- Good command of written & oral English.- Ideal person is a well-organized team player, able to solve on-site problems independently, and with good interpersonal skills.- Integrity and honesty.- Willing to travel frequently.- Healthy body without color blindness and sight weakness.Job Types: Full-time, ContractContract length: 36 months

We have vacant of 1 Quality Assurance Executive Job in Aurangabad, Experience Required : 5 Years Educational Qualification : Post Graduate Diploma Skill Quality Assurance, QC Inspection, Quality Control etc.

Senior Quality Assurance Officer Executive: (Vapi) Job Location: VapiQualification: M.Sc. (Chemistry) or B.Pharm or M.Pharm. Experience: 5 to 7 years experience in a Cosmetic/API/Pharmaceutical Product manufacturing company. He has to review and prepare SOPs.He is responsible for deviation management.He is also responsible for change control management.He is responsible for CAP management.He has to prepare and review BPR & BMR.He is responsible for in process quality assurance.He has to prepare market complaint investigation report/He has to prepare annual quality product review.He has to prepare protocol and report for process validation.He is also responsible for qualification of equipments and manufacturing process.He has to conduct internal audits.Salary: Best in Industry.Share me resume on career.talenthunt.th@gmail.com / cv.talenthunt1@gmail.com Whatsapp me on 7016504771 / 9998137070.

Job Openings for 3 Pharmaceutical Quality Assurance Executive Jobs with minimum 2 Years Experience in Siltara, Raipur, having Educational qualification of : B.Pharma, M.Pharma with Good knowledge in Quality Check, Hplc, Uv-visible Spectrophotometer, LAB Testing, Pharmaceutical Quality Control, Quality Analysis, Testing etc.

Responsibilities:* Conduct HPLC analysis on raw materials & finished products.* Ensure compliance with GLP guidelines during formulation & manufacturing.* Perform UV testing, dissolution assays for tablets/capsules.

Key Responsibilities:1. Conduct inspections and quality checks on raw materials, in-process goods, and finished products.2. Maintain accurate records of test results, certifications, and quality metrics.3. Assist in the calibration and maintenance of testing equipment.4. Identify and report non-conformities, initiating corrective actions as required.5. Support the production team by providing real-time quality feedback and resolving issues.6. Ensure adherence to ISO standards and other industry regulations.Key Skills: Proficiency in using quality testing equipment. Strong analytical and problem-solving skills. Attention to detail and good documentation practices.

Documentation

We have vacant of 1 Quality Assurance Executive Job in Mumbai, Experience Required : 4 Years Educational Qualification : Professional Degree Skill Quality Assurance etc.

Should have Worked in Jewelry Manufacturing Unit. 2. Should have Knowledge of Manufacturing Studded Jewelry

Designation:- Quality AssuranceQualification:- BSc Or MSc Or B.Pharma Or M.PharmaExperience:- 10 Years (Min 5 Years In One Company, Preferable In Pharma Company Knowledge Of ISO 9001-2015 & GMP (Good Manufacturing Practice Is Required)Salary:- 4.5 LPAGender:- Male Or Female Job Location:- Umbergaon, Gujarat Industry:- Manufacturing Company

Qualification:- BSc Or M.Sc In Microbiology Experience:- 2Years To 3 Years Salary:- As Per Interview Job Responsibilities:- i) Day to day QC department activity - Micro and Chemical testing, physical inspection of products, records maintaining etcii) Preparing, Maintaining and taking care of QA / QC documents of all kinds including certificates, calibration, test results, inspection reports, non-compliance reports etc.iii) Document work on computer like SOPS, formats etc.iv) Handling and working on all instruments related QCv) Cary out inspection and checking for all quality related procedures---------------------------------------------Job Location:- Umbergaon, Gujarat

Qualification:- Diploma/B. Tech Mechanical Experience:- 3 to 6 YearsKey Responsibilities:- Overall ARS Incoming Inspection of ink , Tip Refill NPD Daily Report & MISSkill Required:- ARS Process Ink Tip Refill System Refill,ink /Tip Testing MS Office SAPSalary:- 3.5LPA to 4.0 LPAGender:- Male Vacancies:- 01Job Location:- Umbergaon GujratIndustry Manufacturing Company.

Senior Quality Assurance OfficerExecutive: (Vapi) Job Location: VapiQualification: M.Sc. (Chemistry) or B.Pharm or M.Pharm. Experience: 5 to 7 years experience in a Cosmetic/API/Pharmaceutical Product manufacturing company. He has to review and prepare SOPs.He is responsible for deviation management.He is also responsible for change control management.He is responsible for CAP management.He has to prepare and review BPR & BMR.He is responsible for in process quality assurance.He has to prepare market complaint investigation report/He has to prepare annual quality product review.He has to prepare protocol and report for process validation.He is also responsible for qualification of equipments and manufacturing process.He has to conduct internal audits.Salary: Best in Industry.Share me resume on career.talenthunt.th@gmail.com / cv.talenthunt1@gmail.com Whatsapp me on 7016504771 / 9998137070.

Responsibilities:Quality Inspection & Testing:Perform thorough quality inspections of incoming raw materials, in-process components, and finished goods as per established Quality Control Plans and specifications.Conduct various tests (e.g., dimensional checks, functional tests, visual inspections) using appropriate inspection tools and equipment (e.g., Vernier calipers, micrometers, gauges, CMM, software testing tools).Verify product/service against drawings, specifications, and quality checklists.Defect Identification & Reporting:Identify, categorize, and document any defects, non-conformities, or deviations from quality standards.Initiate Non-Conformance Reports (NCRs) and ensure proper containment of defective materials/products.Report critical quality issues immediately to the supervisor and relevant departments.Documentation & Record Keeping:Maintain accurate and organized records of all quality inspections, test results, non-conformities, and corrective actions taken.Prepare daily/weekly/monthly quality reports, summaries, and trend analyses.Ensure all quality documentation is up-to-date and easily retrievable.Standard Adherence & Compliance:Ensure strict adherence to company quality management system (QMS) procedures, work instructions, and industry standards (e.g., ISO 9001, industry-specific standards like IATF 16949, ISO 13485, or GMP, depending on the sector).Assist in maintaining compliance with relevant regulatory requirements.Root Cause Analysis Support:Support the QA/Production team in investigating the root causes of quality issues, customer complaints, and recurring defects.Assist in implementing and verifying corrective and preventive actions (CAPA).Process Monitoring:Monitor production processes and operational steps to ensure quality parameters are being met at each stage.Provide feedback to production personnel on quality concerns and best practices.Equipment Management Support:Assist in the calibration and maintenance of inspection, measuring, and test equipment (IMTE).Continuous Improvement Contribution:Participate in and support quality improvement initiatives (e.g., Lean, 5S, Kaizen, Poke-Yoke) to enhance product quality, process efficiency, and reduce waste.Safety & Housekeeping:Adhere to all workplace safety protocols and maintain good housekeeping practices in the inspection areas.Communication (Local Emphasis):Communicate clearly and effectively with production teams, supervisors, and other internal departments regarding quality issues and requirements.Fluency in Marathi and Hindi is essential for effective interaction with shop-floor staff and local vendors. Good English proficiency is required for documentation, understanding specifications, and interaction with senior management.

Responsibilities:Inspection & Testing:Conduct thorough quality inspections of incoming raw materials, in-process components, and finished goods as per defined specifications, control plans, and sampling procedures.Perform various tests (e.g., dimensional checks, functional tests, visual inspections, destructive/non-destructive tests, as applicable to the product/industry) using appropriate measuring instruments and testing equipment.Operate and maintain quality testing instruments and equipment, ensuring their proper functionality and calibration status.Defect Identification & Reporting:Identify, document, and report any non-conformities, defects, or deviations from quality standards immediately.Segregate non-conforming materials/products and ensure proper tagging and disposition.Generate clear and concise inspection reports and test summaries.Documentation & Record Keeping:Maintain accurate and organized records of all quality inspections, test results, non-conformity reports, and corrective actions.Assist in preparing and updating quality documentation, including inspection checklists, standard operating procedures (SOPs) for quality processes, and quality control plans.Standard Adherence & Compliance:Ensure strict adherence to company quality policies, procedures, and relevant industry standards (e.g., basic understanding of ISO 9001 principles, product-specific standards like BIS, etc.).Monitor production processes to ensure that quality parameters are consistently met at various stages.Root Cause Analysis Support:Assist senior QA personnel or engineers in investigating the root causes of quality issues, customer complaints, and recurring defects.Support the implementation and verification of corrective and preventive actions (CAPA).Calibration Support:Support the periodic calibration of inspection and testing equipment, maintaining calibration records, and ensuring the availability of calibrated instruments.Feedback & Communication:Provide timely feedback on quality issues to the Production team, informing them of deviations and assisting in immediate rectification.Communicate effectively with supervisors, engineers, and other departmental personnel regarding quality matters.Continuous Improvement:Actively participate in quality improvement initiatives, such as 5S, Kaizen, and waste reduction efforts on the shop floor.Safety & Housekeeping:Adhere to all safety regulations and good housekeeping practices in the workplace, especially in testing and inspection areas.Local Communication:Communicate clearly and effectively with the production team, supervisors, and other colleagues. Fluency in Marathi and Hindi is essential for effective interaction on the shop floor. Good English proficiency is required for documentation and technical understanding.

Job Description:1) Closely communicate with the Inspection Coordinators to schedule the inspection assigned.2) Implement inspection according to operation guidelines, inspection guidelines, and any special instructions provided by the company.3) Complete the inspection report with photos and submit it to Technical Manager within the required time limit.4) Submit the inspectors job expense claim form and reimbursement documents monthly and meet financial requirements.5) Perform other duties and responsibilities as assigned by supervisor/management.Requirements:- College graduate or above.- Major in Engineering (Textile, Furniture, Mechanical, Electronic, etc.)- Having more than 1 year more working experience in the inspection field or quality control background of products of Softlinesor Hardlines.- Familiar with the AQL standard and good knowledge of safety and regulation standards.- Good command of written & oral English.- Ideal person is a well-organized team player, able to solve on-site problems independently, and with good interpersonal skills.- Integrity and honesty.- Willing to travel frequently.- Healthy body without color blindness and sight weakness.Job Types: Full-time, ContractContract length: 36 months

Job Description:1) Closely communicate with the Inspection Coordinators to schedule the inspection assigned.2) Implement inspection according to operation guidelines, inspection guidelines, and any special instructions provided by the company.3) Complete the inspection report with photos and submit it to Technical Manager within the required time limit.4) Submit the inspectors job expense claim form and reimbursement documents monthly and meet financial requirements.5) Perform other duties and responsibilities as assigned by supervisor/management.Requirements:- College graduate or above.- Major in Engineering (Textile, Furniture, Mechanical, Electronic, etc.)- Having more than 1 year more working experience in the inspection field or quality control background of products of Softlinesor Hardlines.- Familiar with the AQL standard and good knowledge of safety and regulation standards.- Good command of written & oral English.- Ideal person is a well-organized team player, able to solve on-site problems independently, and with good interpersonal skills.- Integrity and honesty.- Willing to travel frequently.- Healthy body without color blindness and sight weakness.Job Types: Full-time, ContractContract length: 36 months