QA 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,'

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.

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

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

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.

- 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.

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

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

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 looking for 05 QA Executive Posts in Ankleshwar, Bharuch, Gujarat, with deep knowledge in Documentation, QA-Quality Assurance, Pharma, Quality Control and Required Educational Qualification is : B.Pharma, B.Sc, M.Pharma, M.Sc

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

We are third party nutraceutical manufacturer.Job description:Responsible for quality system in company.Co-ordinate with cross functional team for smooth execution and proper documentation of product and system.Responsible to make SOP and formats as and when required for any system for improvement.Knowledge of FSSAI guidelines added advantageQualification: B.pharm/ MSc

We have Vacant of 5 Qa Officer Jobs in Ahmedabad, Gujarat, Quality Assurance Executive, Api Pharma Industries, Experience Required : 2 Years Educational Qualification : B.pharma, B.sc, M.pharma, M.sc Skill Quality Assurance Executive, Api Pharma Industries Etc.must Be Work in Api Pharma Manufacturing Industries,

JOB PROFILE:1.Should be very good in communication and team-leading with a positive approach2.Should have experience in electronics repair like mobile phones, set-top box, etc.3.Should have experience in in-process, final inspection and pre-delivery inspection, etc. in quality department4.Should have knowledge of ISO 9001:2015 (QMS) & expertise in preparing WI, SOPs, etc.5.Can provide quality training and skill matrix cards according to the training plan6.Should have aware of quality tools like 5S, Kaizen, 3M, ESD, 7QC, etc.7.Must have experience in root cause analysis, CAPA, and 8D.8.Must have knowledge of internal/external and third-party audits9.Should have good knowledge in MIS, computer skills and data analysis

Diploma & Degree Mechanical Fresher EngineerWed like to hire a new Employee for our Production, Quality department.Were looking for a Fresher Diploma, Degree in Mechanical & Electrical Engineer with relevant academic scores, and good knowledge about manufacturing industries.This is a Trannys Engineer position job and the salary range is 11k to 15 k/month CTC. Attached youll find the detailed job description.First, I would like clarification about the Job Profile of a candidate in this company:* For Diploma and Degree Engineer- Production and Quality Engineer- DET/GET basis job profile- Job -Location: Ahmedabad, Sanand, Baroda- 8 HOUR Duty (Sunday off)- 17,000 to 20600 salary per month- Transportation and Canteen Available- Companies will give you proper designation according to your experience but your work performance matters most and first.- So Dont worry about your job profile, just think about what you can learn from these MNC companies and how it will give you benefits.- Just search the company profile and think about it.Ideally, wed like to have our new hire on board this week. So, we should have a shortlist of a bunch of candidates by the end of the week. Please let me know if this sounds like a reasonable time frame for a particular position.Feel free to reach out if you need me to clarify the qualification criteria or the scope of responsibilities. Im also happy to answer any other questions you may have about the position.

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 candidate QA with good experience and exposure for the below mentioned role and responsibilities: 3-5 years experience in Quality assurance department. Preparation and implementation of SOPs Manage training at regular interval Preparation, Issuance and Review of documents like Log books, STP, formats used in R&D and ADL. Maintain Technology transfer documents and requirements as per SOP Review of method development and validation of documents Salary- the best in Industry

Designation: Quality Control ExecutiveQualification: Diploma/Degree in printing and Packaging.Reporting To: QC Team lead.Experience: Minimum 3-4 years. (Preferably in quality and production department)CTC Cost : 4 to 5.5 LacsSkills Needed:Computer literateOn site job approvalsKnowledge of colour ManagementExperience in offset/ Flexo paper base printing.

* For Diploma and Degree Engineer- Production and Quality Engineer- DET/GET basis job profile- Job -Location: Ahmedabad, Sanand, Baroda- 8 HOUR Duty (Sunday off)- 15,000 to 20600 salary per month- Transportation and Canteen Available- Companies will give you proper designation according to your experience but your work performance matters most and first.- So Dont worry about your job profile, just think about what you can learn from these MNC companies and how it will give you benefits.- Just search the company profile and think about it.Ideally, wed like to have our new hire on board this week. So, we should have a shortlist of a bunch of candidates by the end of the week. Please let me know if this sounds like a reasonable time frame for a particular position.Feel free to reach out if you need me to clarify the qualification criteria or the scope of responsibilities. Im also happy to answer any other questions you may have about the position.

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

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.

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

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, GujaratBharuch, Ahmedabad, VadodaraJob descriptionManage release of product batches, including owning the QA product release workflow in SAP.Lead and supervise a team of QA professionals to perform operations as described above.Review and approve Purchase Specifications and Analytical StandardsRequired Candidate profileWork to create an environment of open communication,participation &information-sharing within & between teams within QA &throughout facility

QA Executive For Agro chemical Industry In Saykha,Bharuch, GujaratCapital Placement Services4 - 9 years4-6 Lacs P.A.Bharuch, Ahmedabad, VadodaraJob descriptionManage release of product batches, including owning the QA product release workflow in SAP.Lead and supervise a team of QA professionals to perform operations as described above.Review and approve Purchase Specifications and Analytical StandardsRequired Candidate profileWork to create an environment of open communication, participation &information-sharing within & between teams within QA &throughout facilityPls mention thisFeel free to reach me emailVisit our website for more details:Follow Capital Placement Services Linkdein Profile for more updates :