Officer Quality Assurance

**Job Title: Quality Check (QC) and Quality Ana (QA)** **Location: [AMHEDABAD]** **EXPERINCES: Minimum 2+year.** **Salary: 25k to 35k** **Qualification: Bachelor’s degree in Pharma preferred.** **Job Type: [Full-time]** **Job Time: 9 to 6** **Job Overview**: We are seeking a detail-oriented and proactive Quality Check (QC) and Quality Assurance (QA)...

Quality Assurance Exp: Fresher Qualification: / M.pharm / B.pharm Dholka Ahd Pay: From ₹15,000.00 per month Work Location: In person

Quality Assurance Exp: Fresher Qualification: M.pharm / B.pharm Ahemdavad gujrat Pay: From ₹16,000.00 per month Expected Start Date: 05/10/2025

Quality Assurance Exp: Fresher to 1 year Qualification: ( M.pharm / B.pharm Requierd) M.sc / B.sc are not applied Vatva Hathijan Ahemdavad Pay: From ₹13,000.00 per month Work Location: In person

To review documentation of manufacturing and packaging. Retrieve electronic scans and review batch records based on cGDP, cGMP, CPC’s SOPs, and FDA guidelines. To perform batch data entry for APR and process validation. Preparation of Annual Product Review / Product Quality Review reports. To review the process validation report. Pay: From ₹18,000.00...

Job descriptionJob Responsibilities :The Quality Assurance Officer will be responsible for establishing, implementing, and maintaining the Quality Management System of the organization.Ensuring compliance with applicable regulatory requirements and industry best practices.They will oversee quality control and assurance processes, conduct audits and implement...

This position is responsible for managing all cGMP aspects of Quality Assurance Operations of a WHO-GMP & GLP approved Tablets and Capsule manufacturing facility. **Specific Responsibilities**: - Review and approve SOPs, Batch Records, test methods, test results, labeling materials, specifications, analytical validation protocols and reports, stability...

This position is responsible for managing all cGMP aspects of Quality Assurance Operations of a WHO-GMP & GLP approved Tablets and Capsule manufacturing facility. **Specific Responsibilities**: - Review and approve SOPs, Batch Records, test methods, test results, labeling materials, specifications, analytical validation protocols and reports, stability...

**Your responsibilities**: - Review and analyze requirements, specifications, and technical design documents, providing timely feedback - Develop detailed, comprehensive, and well-structured test plans and test cases - Design, develop, and execute automated tests - Test current products and identify deficiencies - Identify and report issues found, then...

**Objectives of this role** - Contribute to the ongoing processes of assurance and enhancement of quality in the work of the department - Enhance the reputation of the department, and meet external demands for demonstrating quality, quality assurance, and quality enhancement - Compile thorough and complete documentation of the work...