Quality Assurance Executive Job Vacancies in Gujarat

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,'

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.

To handle manufacturing sites as a corporate quality control.To do sites audits, contract lab audits and vendor qualification.Preparation of Vendor Audit schedule and to coordinate with various site for the Audit as per schedule.Responsible for compilation and maintenance of vendor qualification documents.Responsible for the preparation of CQA SOPs and to ensure system harmonization.Plan, execute, and oversee product inspection and testing for quality and conformance to specifications and deliverables.Investigate reports of product quality issues and ensure resolution in accordance with company guidelines and regulatory requirements.Stay updated on industry trends, new quality management methodologies, and regulatory changes that affect product quality.

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.

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

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.

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Inspecting: Inspecting materials, products, and operations to ensure they meet standardsTesting: Testing products for functionality, durability, and safetyMeasuring: Measuring products with calipers, gauges, or micrometersMonitoring: Monitoring operations to ensure they meet production standardsRecommending: Recommending adjustments to production or assembly processesDocumenting: Recording inspection results and deviationsCommunicating: Communicating defects to supervisors and collaborating on solutionsAuditing: Preparing for audits, conducting audits, and recording evidenceReporting: Providing quality reports and compiling audit reportsEnforcing: Developing and enforcing protocols to optimize inspection processes

- Full-time on-site role for a Senior Quality Assurance Executive.- Responsible for ensuring products meet internal and external quality requirements.- Ensure compliance with Good Manufacturing Practice (GMP).- Conduct quality audits and manage overall quality control and assurance operations.

Responsibilities:Perform quality control inspections and tests on machinery components and assemblies.Ensure compliance with engineering specifications, standards, and customer requirements.Identify and resolve quality issues through root cause analysis and corrective actions.Conduct inspections at various stages of production to ensure adherence to quality standards.Document inspection results, generate reports, and maintain quality records.Collaborate with production teams to implement quality improvements and process optimizations.Participate in supplier evaluations and quality audits as needed.Support in the development and implementation of quality assurance procedures.Qualifications:Bachelors degree in Mechanical Engineering or related field.Proven experience in quality control within a manufacturing environment, preferably in machinery or equipment.Strong knowledge of quality inspection and testing techniques.Familiarity with quality management systems and tools (e.g., ISO standards).Excellent analytical and problem-solving skills.Effective communication skills and ability to work collaboratively in a team environment.

We have an urgent opening for Quality Assurance Executive for a leading Chemicals Mfg CompanyJob Profile: Quality Assurance ExecutiveLocation: AnkleshwarSalary Range Approx- 4-5LPA Experience - 4 or 5 years only pharma line (API experience )REPORTING TO : Head QARESPONSIBILITIES:1. To issue the Batch Manufacturing Record, Equipment cleaning record, Logbooks, Analytical Report for raw material, finish product and packing material.2. Assistance in preparation of SOP of various departments/ preparation of draft SOPs. 3. During plant round QA Executive to verify documents as per cGMP and GLP norms.4. Line Clearance activities for manufacturing and packaging before process starts.5. To issue the deviation form, Change control form, Out of Specification form, Customer complaint form, OOT form, investigation for etc. as per request from respective dept.6. Review and verification of Analytical and Batch Manufacturing Record and filing BMR. QA verification and release of finish product.7. To prepared documents & records and monitoring of activities as per SOPs8. Distribution, retrieval and control of SOPs, documents/records of all dept.9. To participate the internal audits, customer audit, regulatory inspection.10. To Attend QR meeting as per schedule.11. To ensure data integrity as per procedure.12. To review manufacturing, store, QC activity.13. To prepare approved vendor list and maintain vendor qualification.14. Conduct traceability Activity.15. Preparation and maintain CAPA log.16. To ensure that deviations, product recall, return goods and customer Complaints, OOS, OOT by CAPA and Root Cause analysis are investigated, fill up of report and log the same.17. To collect data and prepare the annual product review.18. To witness and verify process validation, cleaning validation and equipment qualification and to prepare protocol and report. 19. Returned Material: Investigate and make

Review and update standard operating procedures (SOPs) to align with changing regulations and best practices. Documentation And Records Management- Maintain and manage documentation related to quality assurance activities, including batch records, investigation reports, change controls, and validation documentation.- Ensure accurate and timely completion of all quality-related documentation. Product Quality Control- Investigate product non-conformances, deviations, and customer complaints to identify root causes and implement appropriate corrective and preventive actions (CAPAs).- Knowledge of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant quality standards.- Making decisions on batch disposition and product recall based on root cause identification.- Reviewing and approving compliance reports following external (customer/regulatory) audits and corporate audits to ensure compliance.- Preparing and implementing quality assurance policies and procedures and ensure that standards and safety regulations are observed.- Timely completion of APQR related activity- Prepared & Review of Validation protocol and report (like Process Validation, Cleaning Validation, Analytical Method Validation,)- Handling of Market Complaint and Related Compliance- Handling of out of specification and suitable investigation- Handling of Deviation and Incident- Prepared BMR, SOP, Protocols etc.- Compliance of Vendor Audit, Regulatory Audit etc.Skills & QualificationEducation:UG: B.Sc / B.PharmPG: M.Sc / M. PharmKnowledge of computer competence, including database managementMinimum Experience Required: 1 - 3 YearCV Required

We are Urgently Hiring for Qc Executive. Quality Check, and Field Work

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 Title: Executive/Sr ExecutiveDepartment: QAExperience Required: 5 to 10 yearsSalary - 4-7 LpaJOB DUTIES AND RESPONSIBILITIES (Please Mention In Below Table)1 Manage release of product batches, including owning the QA product release workflow in SAP.2 Lead and supervise a team of QA professionals to perform operations as described above.3 Review and approve Deviation and Laboratory Investigations4 Review and approve Purchase Specifications and Analytical Standards5 Review and approve Issue Reviews and CAPA6 Assist with Non-Conformance Investigations and provide guidance in identifying potential product impact and determination of final product disposition7 Review and update Standard Operating Procedures (SOPs) for GMP compliance8 Follow all regulatory guidelines, cGMP guidelines, Environmental Health and Safety regulations as required by the job function Review validation protocols and completed documents, including process qualification protocols for validations of commercial processes.9 Work to create an environment of open communication, participation and information-sharing within and between teams within QA and throughout facility

Dear Candidates,Greeting from the wholesome foods,We are opening for a Quality Executive, Are you looking for a job change?If you are interested so please share your updated CV &Please share below detailsTotal Experience :Current CTC :Notice period :(Location : Kheda-Bareja Highway, Gujarat)(Salary : 18k to 25 k )(Experience : 0 to 3 yearLook forward to hearing from you. ThanksHRPrashant GohelWholesome Foods

Reviewing documentation relating to raw materials and the release of raw materialsReviewing and Preparing batch release documentationReviewing and Approval of QA-controlled documentation (such as SOPs, batch records, working instructionsAuthorization of all procedures and standard instructions of process, controls etc Investigation and closure of all deviations, OOS and complaintsConducting self inspections.Conducting vendor evaluation of raw materials. Should have sound knowledge of Process validation. Should be familiar with preparation of process validation protocol and report.Should have sound knowledge of QMS System and Change Control , Deviation and CAPA Procedure.Review of Preventive maintenance & calibration of equipment and systems.Review of stability data to support retest or expiry dates and storage conditions and/or intermediates where appropriate.Risk analysis evaluationPerforming product quality reviews.Must understand standard operating procedure.

We are looking for a quality engineer to monitor and improve the quality of our operational processes and outputs. The quality engineer's responsibilities include designing quality standards, inspecting materials, equipment, processes, and products, developing quality control systems, and determining corrective actions. You will also work with managers and supervisors to implement quality measures.A successful quality engineer should have excellent troubleshooting skills and be able to ensure that processes and products consistently meet established quality standards.Quality Engineer Responsibilities:Developing and implementing quality standards.Developing and implementing quality control systems.Monitoring and analyzing quality performance.Inspecting and testing materials, equipment, processes, and products to ensure quality specifications are met.Collaborating with operations managers to develop and implement controls and improvements.Ensuring that workflows, processes, and products comply with safety regulations.Investigating and troubleshooting product or production issues.Developing corrective actions, solutions, and improvements.Reviewing codes, specifications, and processes.Quality Engineer Requirements:Degree in quality, industrial, or mechanical engineering.ASQ certification preferred.1+ years of experience in quality engineering, quality assurance, or a similar role.Experience coding and using QA software tools and processes.Strong communication and interpersonal skills.Strong analytical and problem-solving skills.Excellent project management skills.

Dear Candidates,Greeting from the wholesome foods,We are opening for a Quality Executive , Are you looking for a job change?If you are interested so please share your updated CV & Please share below detailsTotal Experience :Current CTC :Notice period :(Location : Kheda, Gujarat) (Experience : Fresher To 1 year )(Salary :13k To depends on experience )Look forward to hearing from you. ThanksHR Prashant GohelWholesome Foods

Job descriptionPreparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis of raw materialsRequired Candidate profileExperience in handling instruments like UPLC, LC-MS , GC, ICP-OES, XRD and DSC.Role: QA / QC ExecutiveIndustry Type: Fertilizers / Pesticides / Agro chemicalsRole Category: Production & ManufacturingSheetal Tanwar

QA Executive For Agro chemical Industry In Saykha,Bharuch, GujaratJob Title: Executive/Sr ExecutiveDepartment: QAExperience Required: 5 to 10 yearsSalary - 4-7 LpaJOB DUTIES AND RESPONSIBILITIES (Please Mention In Below Table)1 Manage release of product batches, including owning the QA product release workflow in SAP.2 Lead and supervise a team of QA professionals to perform operations as described above.3 Review and approve Deviation and Laboratory Investigations4 Review and approve Purchase Specifications and Analytical Standards5 Review and approve Issue Reviews and CAPA6 Assist with Non-Conformance Investigations and provide guidance in identifying potential product impactand determination of final product disposition7 Review and update Standard Operating Procedures (SOPs) for GMP compliance8 Follow all regulatory guidelines, cGMP guidelines, Environmental Health and Safety regulations as required by the job function Review validation protocols and completed documents, including process qualification protocols for validations of commercial processes.9 Work to create an environment of open communication, participation and information-sharing within and between teams within QA and throughout facility10 Work to create an environment of open communication, participation and information-sharing within and between teams within QA and throughout facility11 Assist with complaint investigations for internally produced commercial product12 Ensure compliance to all compendial, internal and client-specific requirements (SOPs, Quality Agreements, General and Informational Chapters in multiple compendia as applicable).13 Ensure all work is performed and documented according to approved standard operating procedures, in general compliance with cGMPs and in a timely manner consistent with agreed upon schedulesIf any candidates is suitable for this opening please sent me your updated profile on this mail id.

QA Executive For Agro chemical Industry In Saykha,Bharuch, GujaratJob Title: Executive/Sr ExecutiveDepartment: QAExperience Required: 5 to 10 yearsSalary - 4-7 LpaJOB DUTIES AND RESPONSIBILITIES (Please Mention In Below Table)1 Manage release of product batches, including owning the QA product release workflow in SAP.2 Lead and supervise a team of QA professionals to perform operations as described above.3 Review and approve Deviation and Laboratory Investigations4 Review and approve Purchase Specifications and Analytical Standards5 Review and approve Issue Reviews and CAPA6 Assist with Non-Conformance Investigations and provide guidance in identifying potential product impact and determination of final product disposition7 Review and update Standard Operating Procedures (SOPs) for GMP compliance8 Follow all regulatory guidelines, cGMP guidelines, Environmental Health and Safety regulations as required by the job function Review validation protocols and completed documents, including process qualification protocols for validations of commercial processes.9 Work to create an environment of open communication, participation and information-sharing within and between teams within QA and throughout facility

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.

Key Responsibilities Review and update standard operating procedures (SOPs) to align with changing regulations and best practices. Documentation And Records Management Maintain and manage documentation related to quality assurance activities, including batch records, investigation reports, change controls, and validation documentation. Ensure accurate and timely completion of all quality-related documentation. Product Quality Control Investigate product non-conformances, deviations, and customer complaints to identify root causes and implement appropriate corrective and preventive actions (CAPAs). Knowledge of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant quality standards. Making decisions on batch disposition and product recall based on root cause identification. Reviewing and approving compliance reports following external (customer/regulatory) audits and corporate audits to ensure compliance. Preparing and implementing quality assurance policies and procedures and ensure that standards and safety regulations are observed. Timely completion of APQR related activity Prepared & Review of Validation protocol and report (like Process Validation, Cleaning Validation, Analytical Method Validation,) Handling of Market Complaint and Related Compliance Handling of out of specification and suitable investigation Handling of Deviation and Incident Prepared BMR, SOP, Protocols etc. Compliance of Vendor Audit, Regulatory Audit etc.Skills & QualificationEducation: UG: B.Sc / B.PharmPG: M.Sc / M. Pharm Knowledge of computer competence, including database managementMinimum Experience Required: 1 - 3 YearCV Required

Job Description for DETIGET We'd like to hire a new Employee - Fresher Diploma/BE, B.Tech -Electrical/EC/Mechanical our Production and Quality department for Manufacturing industries Designation: Diploma Engineer Trainee, Graduate Engineer Trainee on payroll initially Good performers will be taken on company rail during 01 year to 03 year Key Responsibilities: Works under the close supervision of Production shift in charge. Learn Production line under the close supervision of Production shift in charge Overhauling of all machines in the production line as per the annual scheduled Production plan. Line Leading, supervisor, Machine production, Programming Operating knowledge, Quality Inspection Assurance. 5s, hygiene, Discipline etc adaptive nature Participate and ensure adherence to safety norms. Complete preventive/predictive maintenance activities all elated in the shift.Use of technology enablement/ automation requirements for processes.implementation of SOP and guidelines for data management, maintenance and. Maintain oversight, ensuring effective adherence of the policies.

QC Chemist Jobs in AhmedabadBSC MSC QC Chemistry Job Vacancy in Ahmedabad for FreshersHiring for Pharma Quality Control in AhmedabadPosition Name - QC ChemistJob Location SANNAD & Changodar GIDC, AhmedabadTotal Openings 15 Male/FemaleQualification Any GraduatesIndustry Food & PharmaExperience Min 1 to 3 Yrs exp as QA/QCSalary up to 15K - Depends on Exp6 Days Working Monday to SAT 9am to 6pmSkills & Job Descriptions Checking of raw material, in process raw material and finished goods as per the inhouse quality parameters To evaluate parameters such as refractive index, specific gravity, and also organoleptic test like,Seeing/sight, appearance, olfactory notes of perfumery compounds and flavors Blending/stirring, sample preparation, record keeping, documentation of daily qc work Person should be aware of ERP systems Such as SAP and Any other systems. Person should maintain laboratory work properly. Person should know about FSSAI rules and other legal requirements