Quality Assurance Executive Job Vacancies in Ahmedabad

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.

Documentation

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

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

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

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.

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,

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* 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.

Candidate should be responsible for Maintaining records of quality of incoming material and raise complain in case of deviations Candidate should be having knowledge of costing, accounts He need to follow up with supervisors regarding incoming report and material received He needs to ensure material is received as per the contract Responsible for tracking and reporting quality concerns Communication skills (Reading, writing and speaking) in English must be very good. Good Knowledge Import Procedures is preferable Candidate should be responsible for quality claim.

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

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