Quality Assurance Executive Jobs in India

We are looking for a Pharmaceutical Quality Assurance Executive to ensure that our products meet the highest standards of quality and safety. This role is ideal for recent graduates or those with up to five years of experience in the pharmaceutical industry.Key Responsibilities:1. **Quality Audits**: Conduct routine inspections and audits of production processes to ensure compliance with quality standards and regulatory requirements.2. **Document Control**: Manage and maintain quality documentation, including standard operating procedures (SOPs) and quality manuals, ensuring all records are up to date and accurate.3. **Product Testing**: Collaborate with laboratory teams to perform sample testing and analyze results, guaranteeing that products meet established quality specifications before release.4. **Problem Resolution**: Identify quality issues, investigate root causes, and recommend corrective actions to prevent recurrence and enhance overall product quality.5. **Training and Support**: Assist in training staff on quality assurance processes and regulatory requirements, fostering a quality-first culture within the organization.Required Skills and Expectations:Candidates must possess a relevant graduate degree. Strong attention to detail and excellent analytical skills are essential for identifying and resolving quality issues. Clear communication abilities are necessary to effectively collaborate with various teams. A proactive attitude, along with a willingness to learn and adapt in a fast-paced environment, is crucial for success in this role. Familiarity with quality assurance principles and regulatory guidelines in the pharmaceutical sector is a plus.

We are looking for a Quality Assurance Executive with 5 to 10 years of experience in the pharmaceutical industry. The ideal candidate will ensure that all products meet quality standards and comply with regulations. **Key Responsibilities:**- **Quality Control Inspections:** Conduct regular inspections of products to ensure they meet established quality criteria and specifications.- **Documentation Review:** Verify all quality assurance documentation to ensure accuracy and compliance with industry standards.- **Process Improvement:** Identify areas for process enhancements and implement solutions to improve quality and efficiency in production.- **Compliance Checks:** Ensure that all operations comply with local and international quality regulations and standards relevant to the pharmaceutical industry.- **Training and Support:** Provide training and support to employees on quality assurance processes and best practices to foster a culture of quality.**Required Skills and Expectations:**The candidate must possess a B.Pharma or a relevant professional degree, with a strong understanding of quality assurance principles in the pharmaceutical field. Attention to detail and a methodical approach to tasks are essential. The ability to collaborate effectively with cross-functional teams and communicate clearly is crucial. Proficiency in quality management tools and methodologies is expected. Knowledge of regulatory standards governing the pharmaceutical industry will be beneficial. We are looking for a proactive individual who can work independently and make decisions that impact product quality positively.

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

Field Sales Executive - KolkataWe're looking for a driven Field Sales Executive to acquire Businesses and advertisers for our digital screen network in Kolkata. You'll identify potential customers, pitch our benefits (increased foot traffic, targeted audience, ROI), and onboard them. Responsibilities include: Prospecting shopkeepers for screen placement. Pitching ad opportunities to local businesses. Explaining benefits (targeted audience, flexible plans, measurable results)Onboarding customers and ensuring smooth delivery. Meeting sales targets and reporting progress. Collaborating with team for strategy and growthRequired: Sales experience, communication skills, local market knowledge. Commission-based incentives.

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.

Quality engineer for inspection of mechanical components. Should aware about measuring instruments, gauges, etc also experienced in operating computer, ms excel, ms office. Maintaing quality reports, documentation etc

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.

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.

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,'

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

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

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

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).

This Quality Control Executive position in Ahmedabad is open to freshers with a diploma. This role involves ensuring the quality of products meets standards through inspections, testing, and reporting findings to management. Attention to detail, analytical skills, and a strong understanding of quality control processes are essential. The ideal candidate should be a male candidate who can work full time in an office setting.

We are looking for a detail-oriented and technically inclined Quality Executive to ensure the quality and dimensional accuracy of white metal babbitt bearings and related components. The candidate should be capable of understanding mechanical drawings, tolerances, and material specifications. Hands-on finishing work and inspection with measuring instruments will be part of the role.Key Responsibilities:Interpret and understand manufacturing/engineering drawings of components and bearings.Carry out incoming, in-process, and final inspection of components.Use measuring instruments such as Vernier calipers, micrometers, bore gauges, depth gauges, dial indicators, etc.Perform finishing tasks like deburring, filing, polishing, and sandpaper finishing when required to achieve required surface quality.Prepare dimensional inspection reports and maintain quality documentation.Ensure components meet drawing specifications, tolerances, and standards.Check surface finish, alignment, ovality, concentricity, and other critical parameters related to white metal bearings.Monitor material certificates, hardness, and composition where applicable.Raise NCRs (Non-Conformance Reports) and coordinate with production to resolve defects.Implement and support quality control procedures, improvements, and system audits.Ensure workplace cleanliness, safety, and compliance.Skills & Requirements:Diploma/ITI in Mechanical/Production or equivalent qualification.Basic understanding of manufacturing processes of white metal bearings (preferred).Proficiency in measuring tools and dimensional inspection.Ability to read and interpret engineering drawings & GD&T (Geometrical Dimensioning & Tolerance preferred).Knowledge of materials like Babbitt alloys, mild steel, bronze, etc.Good analytical mindset and keen attention to detail.Basic knowledge of MS Excel/Word to prepare inspection reports.Willingness to perform hands-on finishing and shop floor tasks when required.Ability to work in a fast-paced manufacturing environment.

Job Summary Telecaller and field (POI Data Collection)The Candidate will contact restaurants, hotels, shops, tourist attractions, and service providers across Amritsar to collect and verify Point of Interest (POI). The role involves making outbound calls, validating details, and maintaining accurate daily reports.Key Responsibilities:Call and engage POIs to verify business details.Collect information such as contact details, timings, services, pricing, and amenities.;

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.

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.

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.

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.