15 Qa Executive Jobs

04 to 05 Years Experience of QA Documentation . Should be able to conduct IPQA independently. Responsible for Line clearance In-process of all activities. Responsible for review, compilation and closing of Batch manufacturing records and Batch Packing records. Responsible to follow, Good Documentation Practices, Good Manufacturing Practices to ensure the quality standards of company. Verification & monitoring of shop floor activities from dispensing to dispatch. Responsible for manufacturing compliance. Responsible for preparation of relevant SOPs. Monitoring & verification of log books at manufacturing blocks for compliance Desired Candidate Profile The candidate should have adequate knowledge in QA Documation He/ She should have 3-5 years of experience with B. Pharm./ M. Pharm./ educational qualification. Candidate should possess excellent verbal and communicational skills.

Handling of Quality management system like Market complaints, Change Control, Deviations, OOS, OOT, Incidents, CAPA, Self-Inspection, Vendor Qualification. Review and Approval BMR/BPRs, Prepare of Standard Operation Procedure, Process Validation, Hold Time Study Protocol and Reports, Annual Product Quality Review & trending, Cleaning validation. Qualification/ requalification of Equipments. Release of Finished Product, Continuous Process Verification, Trainings etc.

04 to 05 Years Experience of QA Documentation . Should be able to conduct IPQA independently. Responsible for Line clearance In-process of all activities. Responsible for review, compilation and closing of Batch manufacturing records and Batch Packing records. Responsible to follow, Good Documentation Practices, Good Manufacturing Practices to ensure the quality standards of company. Verification & monitoring of shop floor activities from dispensing to dispatch. Responsible for manufacturing compliance. Responsible for preparation of relevant SOPs. Monitoring & verification of log books at manufacturing blocks for compliance Desired Candidate Profile The candidate should have adequate knowledge in QA Documation He/ She should have 3-5 years of experience with B. Pharm./ M. Pharm./ educational qualification. Candidate should possess excellent verbal and communicational skills

•Education: M.Sc. Chemistry/ Environmental Science •Experience: 3-8years •Skills :Titration Methods, ,Calibration of pH meter, Operation of UV Visible Spectrophotometer, & Karl Fischer ,ISO &5S, SAP Contact NO :6359660041

Responsibilities: Inspection & Testing: Perform regular quality inspections and tests on incoming raw materials, in-process production stages, and finished products as per defined quality control plans, specifications, and sampling procedures. Utilize various measuring instruments (e.g., calipers, micrometers, gauges) and testing equipment to ensure accurate data collection. Conduct visual inspections to identify defects, deviations, or non-conformities. Process Monitoring & Compliance: Monitor production processes and operational activities to ensure strict adherence to established Standard Operating Procedures (SOPs), work instructions, and quality management system (QMS) requirements (e.g., ISO 9001:2015). Identify and report any deviations from quality standards or process parameters immediately. Non-Conformance Management: Identify, segregate, and document non-conforming materials or products. Assist in the investigation of root causes for quality issues, defects, or customer complaints. Support the implementation and verification of corrective and preventive actions (CAPA). Documentation & Reporting: Maintain accurate and organized quality records, including inspection reports, test results, non-conformance reports, and calibration records. Prepare daily/weekly/monthly quality reports summarizing inspection findings, defect rates, and other relevant quality metrics for management review. Calibration & Maintenance: Assist in coordinating the calibration and maintenance schedules for all quality control instruments and testing equipment to ensure their accuracy and reliability. Audit Support: Participate in internal and external quality audits (e.g., ISO audits, customer audits, regulatory inspections) by providing necessary documentation and support. Training & Awareness: Assist in providing basic quality awareness training to production staff and new hires on quality procedures, work instructions, and good manufacturing practices. Continuous Improvement: Actively participate in continuous improvement initiatives, contributing ideas and efforts towards enhancing product quality, process efficiency, and reducing waste (e.g., 5S, Kaizen activities). Communication (Local Emphasis): Communicate quality-related information, findings, and concerns clearly and effectively to production teams, supervisors, and other relevant departments. Fluency in Marathi and Hindi is essential for effective interaction with shop-floor personnel. Good English proficiency is beneficial for documentation, technical standards, and communication with senior management or external parties.

Responsibilities: Inspection & Testing: Perform regular quality inspections and tests on incoming raw materials, in-process production stages, and finished products as per defined quality control plans, specifications, and sampling procedures. Utilize various measuring instruments (e.g., calipers, micrometers, gauges) and testing equipment to ensure accurate data collection. Conduct visual inspections to identify defects, deviations, or non-conformities. Process Monitoring & Compliance: Monitor production processes and operational activities to ensure strict adherence to established Standard Operating Procedures (SOPs), work instructions, and quality management system (QMS) requirements (e.g., ISO 9001:2015). Identify and report any deviations from quality standards or process parameters immediately. Non-Conformance Management: Identify, segregate, and document non-conforming materials or products. Assist in the investigation of root causes for quality issues, defects, or customer complaints. Support the implementation and verification of corrective and preventive actions (CAPA). Documentation & Reporting: Maintain accurate and organized quality records, including inspection reports, test results, non-conformance reports, and calibration records. Prepare daily/weekly/monthly quality reports summarizing inspection findings, defect rates, and other relevant quality metrics for management review. Calibration & Maintenance: Assist in coordinating the calibration and maintenance schedules for all quality control instruments and testing equipment to ensure their accuracy and reliability. Audit Support: Participate in internal and external quality audits (e.g., ISO audits, customer audits, regulatory inspections) by providing necessary documentation and support. Training & Awareness: Assist in providing basic quality awareness training to production staff and new hires on quality procedures, work instructions, and good manufacturing practices. Continuous Improvement: Actively participate in continuous improvement initiatives, contributing ideas and efforts towards enhancing product quality, process efficiency, and reducing waste (e.g., 5S, Kaizen activities). Communication (Local Emphasis): Communicate quality-related information, findings, and concerns clearly and effectively to production teams, supervisors, and other relevant departments. Fluency in Marathi and Hindi is essential for effective interaction with shop-floor personnel. Good English proficiency is beneficial for documentation, technical standards, and communication with senior management or external parties.

What We re Looking For: Qualification: M.Sc. Chemistry / B.E. Chemical / B.Pharmacy Experience: 4-6 years in the pharmaceutical industry Strong knowledge in: QMS, Validation (Process, Equipment, Cleaning), and Qualification (IQ/OQ/PQ) Good documentation skills and regulatory understanding: GMP, FDA, ISO

1. CRM portal operations handle by QA. 2. Monitor and review CRM portal complaints, feedback and suggestions and sharing to the concern department. 3. Monitor and review CFA/distributor/dealer/Parlor, Complaint/ feedback and suggestions and sharing to the concern department. 4. Ensure customer/consumer satisfaction/communication after reviewing the corrective action. 5. Reporting and analysing trend report with respect to complaints, feedback and suggestions. 6. Continual improvement, suggestions and updation of portal and trend analysis. 7. Coordination and timely closure of complaints. Teamwork, Food & Beverage, Coordination, Computer, Crm & Portal, Haccp, Sap, 5s Concept

Job Overview: The Quality Assurance professional ensures compliance with regulatory standards, Good Manufacturing Practices (GMP), and company policies to maintain the highest quality of pharmaceutical products. The role involves documentation, audits, validations, and continuous improvement of quality systems. Key Stakeholders: All Department, Customers & Clients on need basis. Reporting Structure: Sr. Manager-QA Experience: 02- 04 Years Role & Responsibilities: Issuance, archival and retrieval of documents Issuance of Control copies to respective dept Destruction of the GMP documents once the retention term has passed and controlled copies of the obsolete GMP documents. Tracking of all QA documents. Maintaining of backup of QA softcopies. Maintaining SOP/s with proper indexing. Preparation and review of SOPs. Management of QA stationary (controlled copies and logbooks) Dispatch and line clearance activities. Review of BMR/BECR Involving in handling of deviations, change control and related CAPAs To ensure data integrity compliances while performing activities. Competencies: Quick learner with excellent communication skills Punctual with proven track record of dedication & reliability A team player who is equally capable of working alone Fluent in both written and spoken English Knowledge /Experience in peptides MSc/BSc, MPharm/BPharm

Kamaths Ourtimes Icecreams Private Limited is looking for QA Executive to join our dynamic team and embark on a rewarding career journey You will also be responsible for identifying and resolving quality-related issues and ensuring that the company's products and services meet the requirements of customers Conduct regular quality audits to identify and resolve quality-related issues Develop and maintain quality metrics to track performance and identify areas for improvement Manage the documentation process for quality assurance procedures, including the creation and maintenance of standard operating procedures (SOPs)

Strong knowledge of FDA regulation, ISO 13485 and QMS principles Qualification : BSc / MSc / B.Pharm / M.Pharm No. of Vacancies : 1 Experience : 1-2 Years in Medical Devices / Pharmaceuticals or Surgical industy

04 to 05 Years Experience of QA Documentation . Should be able to conduct IPQA independently. Responsible for Line clearance In-process of all activities. Responsible for review, compilation and closing of Batch manufacturing records and Batch Packing records. Responsible to follow, Good Documentation Practices, Good Manufacturing Practices to ensure the quality standards of company. Verification & monitoring of shop floor activities from dispensing to dispatch. Responsible for manufacturing compliance. Responsible for preparation of relevant SOPs. Monitoring & verification of log books at manufacturing blocks for compliance Desired Candidate Profile The candidate should have adequate knowledge in QA Documation He/ She should have 3-5 years of experience with B. Pharm./ M. Pharm./ educational qualification. Candidate should possess excellent verbal and communicational skills

Job Title: QA Executive Experience: 6 months to 1 year of full-time experience Mode: Hybrid (2-3 Days Work From Office) Location: Mumbai About Brandintelle Brandintelle is a pioneering enterprise solution that streamlines marketing processes and enables teams to make data-driven, AI-powered decisions. We are a growing startup with a team of 60+ diverse individuals, fostering a close-knit, employee-first culture. At Brandintelle, you ll experience an enriching and fast-paced work environment with opportunities to work on cutting-edge technologies, grow quickly, and contribute meaningfully to impactful projects. What Youll Do as a QA Executive As a Quality Assurance Executive at Brandintelle, you will: Conduct rigorous testing of our platform by identifying, documenting, and following up on bugs or issues. Design and execute comprehensive manual test plans to ensure the platform s functionality and reliability. Assist in implementing and maintaining automation testing frameworks for specific features. Collaborate closely with Developers, Product Managers, and other teams to ensure high-quality and timely product releases. Continuously identify opportunities to improve QA processes and suggest enhancements. What We re Looking For A detail-oriented individual who thrives on troubleshooting and solving complex problems. A proactive team player with a strong sense of responsibility and ownership. Someone eager to grow in a dynamic environment and contribute to the overall success of the product. Requirements 6 months to 1 year of full-time experience in Quality Assurance or related roles. Solid understanding of QA methodologies, testing frameworks, and defect-tracking tools. Basic knowledge of automation testing and scripting languages is a plus. Strong analytical, critical thinking, and communication skills. Knowledge about automation testing is a plus. Why Join Us Work closely with a talented and supportive team. Gain hands-on experience testing and enhancing a leading-edge product for the marketing and advertising industry. Be part of a fast-paced, employee-first culture that values growth and learning. Enjoy flexible working hours and opportunities for professional development. Compensation 3-4 LPA Take the next step in your career as a QA Executive at Brandintelle and contribute to building exceptional user experiences.

B.Sc. / M.Sc. with 3 to 4 years of experience in pharmaceutical industry. Experience of CAPA, change control, QMS, Documentation, SOP Preparation, IPQA, BMR issuance and review, Equipment qualification, GMP/GDP documents, etc. Required Candidate profile To ensure Q. A. activities are carried out as per set procedures and ensure to record in respective documents. Preparation and review of equipment and utility qualifications documents. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Issuance, archival and retrieval of documents Issuance of Control copies to respective dept Destruction of the GMP documents once the retention term has passed and controlled copies of the obsolete GMP documents. Tracking of all QA documents. Maintaining of backup of QA softcopies. Maintaining SOP/s with proper indexing. Preparation and review of SOPs. Management of QA stationary (controlled copies and logbooks) Dispatch and line clearance activities. Review of BMR/BECR Involving in handling of deviations, change control and related CAPAs To ensure data integrity compliances while performing activities. Competencies: Quick learner with excellent communication skills Punctual with proven track record of dedication & reliability A team player who is equally capable of working alone Fluent in both written and spoken English Knowledge /Experience in peptides