QA Executive Jobs in India

Key ResponsibilitiesManagement Representative (MR) Duties: Act as the primary liaison with external certification bodies, customers, and regulatory authorities during system audits; lead internal Management Review Meetings (MRM) with senior leadership.System Maintenance & Compliance: Ensure all plant or corporate processes align with ISO and other industry-specific compliance standards.Documentation & Control: Design, implement, and maintain standard operating procedures (SOPs), quality manuals, work instructions, and documentation control frameworks across all departments.Internal Audit Coordination: Plan, schedule, and execute regular internal system audits; train internal auditors and evaluate audit findings.Corrective & Preventive Action (CAPA): Track non-conformances (NCs) raised during audits, facilitate root-cause analysis with department heads, and monitor the timely closure of CAPAs.Process Improvement: Review operational metrics and KPIs across production, quality, maintenance, and HR to recommend continuous process improvements.

We are seeking a QC Executive with 3 to 5 years of experience to join our team in Joshimath. The ideal candidate will be responsible for ensuring the quality of our products and processes, playing a key role in maintaining high standards.Key Responsibilities:1. **Quality Inspection**: Conduct regular inspections of products and processes to ensure they meet established quality standards. This includes testing materials and finished products.2. **Documentation**: Maintain detailed records of inspections, tests, and quality metrics. This will involve compiling reports to track quality issues and improvements.3. **Problem Resolution**: Identify and analyze quality issues, and work to develop solutions and corrective actions. This may also involve coordinating with other departments to address concerns.4. **Process Improvement**: Assist in reviewing and refining existing quality control processes to enhance efficiency and effectiveness. Propose recommendations based on inspection findings.5. **Compliance**: Ensure that all quality control practices comply with industry regulations and standards. Stay updated with changes in regulations to implement necessary adjustments.Required Skills and Expectations:The successful candidate should have a bachelors degree and a strong background in quality control. Attention to detail and strong analytical skills are essential for identifying issues and implementing solutions. Proficiency in using quality control tools and software is important. Additionally, effective communication and teamwork skills are necessary, as the role involves collaborating with various teams. The candidate should possess a proactive attitude towards maintaining high-quality standards and be willing to take ownership of responsibilities.

Hands On Quality Assurance,Having Knowledge of ProductEnsure Products meet quality standard and performing inspections.Maintaining equipment CalibrationAcceptance sampling, Testing Sample, Track Process Variation over time,'

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.

Hiring Hiring Weblink.in Pvt Ltd is urgently hiring a Manual Tester with 1-2 years of experience in test cases, bug reporting, and test methodologies. The job is located in West Delhi, with a 5-day workweek and a negotiable salary.Job Responsibilities:- Review requirements, specifications, and technical design documents- Develop, document, and execute detailed test cases, test plans, and test scenarios- Perform functional, regression, integration, and usability testing- Identify, report, and track software defects and inconsistencies using bug tracking tools like Jira- Collaborate with developers and QA leads to reproduce issues and validate resolutions- Create detailed, comprehensive, and well-structured test plans and test cases- Execute test cases as per test plans and analyze results- Identify, record, document thoroughly, and track bugs using bug tracking tools- Perform thorough regression testing when bugs are resolvedRequired Skills:- 1-2 years of experience in manual testing- Strong knowledge of manual testing concepts (SDLC, STLC, Test Case Design, Bug Lifecycle)- Experience with writing and executing test cases and test scenarios- Basic understanding of Selenium WebDriver with Java/Python- Familiarity with API testing tools like Postman, REST Assured- Good understanding of database testing (SQL queries, basic DB validations)- Strong analytical and problem-solving skillsCompany Details:*- Company: Weblink.in Pvt Ltd- Location: 33 & 33A, Rama Road, Industrial Area, Near Kirti Nagar Metro Station, West Delhi- Contact Person: Shrijana - Mobile: 93197 59641 - Email: hrd_srijana@weblink.in

Handling of QA Documentation.Drafting of products permission, COPP, MMC.Review of BOM.

Join our team as a Software Executive in Ujjain, India. As a key member of our team, you will be responsible for developing and maintaining software applications, troubleshooting technical issues, and collaborating with the rest of the team to ensure timely project delivery.Key responsibilities include:- Developing software applications based on requirements provided by the team.- Collaborating with team members to troubleshoot and resolve technical issues.- Ensuring all software projects are completed within deadlines.- Providing regular updates to the team on project progress.We are looking for candidates who have completed their 12th pass education and have 0-3 years of experience in software development. The ideal candidate should have strong problem-solving skills, excellent communication abilities, and be able to work independently in a remote work environment. A good understanding of programming languages and software development practices is essential for this role. Apply now to join our dynamic team!

About Company- We are a WHO-GMP Certified company , having 29+ yrs of experience in Pharma sector. Consern's portfolio comprises of over 400+ products and a nexus of prescribing Doctors from Neuro, Gynea, Cardio, Diabetics, Derma, Gastro, Ortho & General health care.Job role- - Review QC doc (Online or Offline)- Review audit trail- Knowledge of QC instruments - Documents for OOS/OOT incident

Job Title: Quality Control Executive / InspectorLocation: Ahmedabad , ChangodarExperience: 12 years of quality control experience in manufacturing, pharma, or medical devices.Job Summary:The Quality Control Executive/Inspector ensures that raw materials, in-process items, and finished products meet defined quality standards and regulatory requirements. The role involves inspection, testing, documentation, and collaboration with production and quality teams to maintain product quality and compliance.Key Responsibilities:Inspect raw materials, in-process products, and finished goods for quality compliance.Perform visual, dimensional, and functional checks using inspection tools.Conduct required product tests and analyze results against specifications.Identify defects, deviations, and non-conformities and report findings.Maintain accurate inspection and test documentation.Support quality audits and ensure compliance with ISO, GMP, and internal standards.Collaborate with production and QA teams to resolve quality issues and drive improvements.Qualifications & Skills:Bachelors degree in Quality, Engineering, Life Sciences, or related field.Knowledge of ISO/GMP standards.Strong attention to detail, analytical skills, and problem-solving ability.Proficiency with inspection tools (calipers, micrometers, gauges).

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 Hiring IPQA & QA for Pharmaceutical Company in Buttibori, Nagpur!!!Job Role: IPQA/QAQualification: B. Pharma / M. Pharma /B.Sc/M.Sc (Chemistry)Experience: Fresher can applySalary: 12,000 - 14,000 kNo. of Vacancies: 10Job location: Buttibori, Nagpur, MaharashtraNote: Up-to Rs 2600 will be provided as a monthly petrol allowances to candidates selectedMale candidates required onlyFor more details and for book your interview, call us on 7517361633

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

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.

Required Candidate from Injectable Pharmaceuticals Background. Should have B. Pharm Graduate. Should have experience of 10-12 Years in Validation & Qualification of Injection Plant.

The Pharmaceutical Quality Assurance Executive is responsible for ensuring compliance with regulatory requirements and company policies to maintain high quality standards for pharmaceutical products. The main responsibilities include:- Implementing and maintaining quality assurance systems and programs to meet regulatory requirements- Conducting internal audits to ensure adherence to standard operating procedures- Developing and implementing quality control procedures for manufacturing processes- Investigating and resolving quality issues and non-conformances- Monitoring and analyzing data to identify trends and areas for improvementQualification: B.Pharma/ M.Pharma/ M.ScSend Resume @7861999933Email id: toscrecruitments@gmail.com

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.

Key Responsibilities:Ensure implementation and compliance with cGMP, GLP, GDP, and regulatory guidelines (WHO, USFDA, EU-GMP, Schedule M).Review and approve Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), SOPs, specifications, and protocols.Handle deviations, change controls, OOS/OOT investigations, CAPA, and risk assessments.Monitor in-process quality checks and finished product documentation.Participate in internal, external, and regulatory audits and ensure timely closure of audit observations.Perform and review validation activities including process validation, cleaning validation, and equipment qualification.Control and maintain QA documentation, logs, and quality records.Coordinate with Production, QC, Engineering, and Warehouse teams for quality-related activities.Support product release and market complaint handling.Ensure compliance with data integrity and documentation practices.Required Qualifications:B.Pharm / M.Pharm / B.Sc / M.Sc (Chemistry or related discipline)1-5 years of experience in Quality Assurance within a pharmaceutical manufacturing environmentStrong knowledge of GMP documentation and regulatory compliancePreferred Skills & Competencies:Hands-on experience with regulatory audits (WHO / USFDA / MHRA)Knowledge of pharmaceutical quality systems (QMS)Good understanding of validation and qualification proceduresStrong analytical, documentation, and problem-solving skillsProficiency in MS Office and quality management systemsGood communication and coordination abilitiesIndustry:Pharmaceuticals / API / Formulations

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.

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.

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.

We have vacant of 2 Quality Control Executive Jobs in Sonipat, HARYANA, Experience Required : 3 Years Educational Qualification : Higher Secondary, Secondary School, B.Tech, Other Bachelor Degree Skill Quality Assurance, Quality Control, QA-quality Assurance, Quality Check, Quality Analysis etc.