QA Executive Jobs

Key Responsibility:- Perform routine chemical and physical analysis on incoming raw materials, in-process batches, and final finished goods. Maintain and track control/retention samples of finished products and raw materials. Write down test results and keep detailed logs following Good Documentation Practices. Operate and maintain key analytical laboratory instruments Execute and document timely calibration and standardization of laboratory instruments to ensure Measurement accuracy. Ensure strict adherence to chemical handling, waste disposal guidelines, and the usage of Personal Protective Equipment (PPE)Qualification & Skills: 2 to 3 years of working experience in a Quality Control laboratory of a Chemical, Understanding of chemical properties, wet chemistry, and analytical methods. Hands-on experience with handling hazardous chemicals safely. Proficient in Microsoft Excel for compiling test data.Share Resume :- palak.hitech@gmail.com

Key ResponsibilitiesShop Floor & IPQA OperationsPerform line clearance for dispensing, manufacturing, filling, and packaging operations.Execute In-Process Quality Assurance (IPQA) checks during production and ensure strict compliance with Master Batch Records (BMR/BPR).Monitor ambient environmental parameters, cleanroom conditions, differential pressure, and water system sampling.Quality Management System (QMS)Handle QMS elements including Deviations, Change Controls, Corrective and Preventive Actions (CAPA), and Out of Specification (OOS) investigations.Conduct root cause analysis (RCA) using tools like 5 Whys and Fishbone diagrams for quality incidents.Coordinate internal audits, self-inspections, and follow up on audit observations to closure.Documentation & Batch ReleaseReview executed Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR) prior to final batch release.Draft, review, and periodically update Standard Operating Procedures (SOPs), Validation Protocols, and Qualification Reports.Prepare Annual Product Quality Reviews (APQR/PQR) and trend reports for Critical Quality Attributes (CQAs).

Designation :- Quality AssuranceDepartment :- Sr officer/ Executive Section :- Regulatory affairs Communication Qualification:- BSC , MSC chemistry/ B Pharma M Pharma Experience :- 6 Years To 7 YearsSalary:- As per interviewGender:- MaleJob Time :- General Shift Vacancies :- 02Job Location:- Boisar, Maharashtra Industry:- Reputed Manufacturing Industry

We are seeking a dedicated QA QC Executive to join our team in Nalagarh. The ideal candidate will have 1 to 4 years of experience in quality assurance and control within a manufacturing or production environment.Key Responsibilities:- Quality Audits: Conduct regular quality audits to ensure compliance with company standards and regulatory requirements. This involves evaluating processes and identifying areas for improvement.- Inspection of Raw Materials: Analyze and inspect incoming raw materials for quality and conformity to specifications. This step is crucial to ensure that only the best materials are used in production.- Testing Products: Perform tests on finished products to verify they meet quality standards and specifications. This includes both visual inspections and functional testing.- Documentation: Maintain accurate records of quality inspections, test results, and corrective actions taken. Clear documentation helps in tracking improvements and ensuring accountability.- Collaboration with Teams: Work closely with production and engineering teams to address quality issues and implement corrective actions. Strong communication ensures everyone is aligned on quality goals.Required Skills and Expectations:Candidates must demonstrate strong attention to detail and analytical skills to identify defects and non-conformities effectively. Proficient knowledge of quality assurance methodologies and tools is essential. The ability to work well in a team environment and communicate findings clearly is necessary. A proactive approach to problem-solving and a strong commitment to maintaining high-quality standards are expected.

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

About Us:Leaders Training Centre (LTC) is a premier professional training provider delivering high-quality programs in business, finance, HSE, and technical disciplines. We are committed to excellence in training delivery, learner experience, and operational efficiency.Position Overview:We are looking for a QA/QC & Process Analyst with proven experience in educational or corporate training environments. The role combines quality assurance, quality control, and process analysis, ensuring our operations meet the highest standards and support smooth delivery of all training programmes.Key Responsibilities:Quality Assurance & Control:Develop, implement, and monitor QA/QC procedures for training operations.Conduct regular audits of learner records, assessments, trainer delivery, and operational workflows.Identify gaps, recommend corrective actions, and track improvement initiatives.Ensure compliance with accreditation standards and internal policies.Process Analysis:Analyze current operational workflows and identify areas for process improvement.Develop and maintain SOPs, process maps, and workflow documentation.Collaborate with teams to implement process improvements for efficiency and quality.Monitor KPIs and provide actionable insights for decision-making.Requirements:Bachelors degree in Business Administration, Management, Quality Management, or a related field.Minimum 23 years of experience in QA/QC, process analysis, or operational management, preferably in education or training environments.Strong knowledge of process optimization, workflow mapping, and quality standards.Experience with Learning Management Systems (LMS) and administrative systems is a plus.Excellent analytical, problem-solving, and organizational skills.Strong communication skills with the ability to work across multiple teams.Detail-oriented, proactive, and results-driven.Why Join Us:Play a key role in improving the quality and efficiency of a growing training centre.Exposure to diverse professional training programmes and sectors.Collaborative and dynamic work environment.Career growth opportunities in operations, quality, and management.

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

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.

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.

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

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.