Quality Assurance Executive Graduate Jobs in Ahmedabad

Documentation

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 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,

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