Quality executive jobs in Vapi

 ...Job Description: Junior Executive – Quality Assurance (USFDA – MYVAL) Experience: 1–3 years in the Medical Device/Pharmaceutical industry Qualification: B.Pharm / M.Pharm / B.Sc. / M.Sc. in a relevant discipline Key Responsibilities: Ensure compliance... 

 ...QMS Management Manage and maintain site Quality Management System procedures. Ensure timely processing and closure of Deviations, Incidents, investigations, CAPAs, Change Controls, and Risk Assessments. Review trend analysis of quality events and identify improvement... 

 ...Actively hiring Us Process Executive Start Date Starts  Immediately CTC (ANNUAL) ₹ 3,00,000 - 3,84,000 ₹ 3,00,000 - 3,84,000 /year... 

 ...Manager Criteria: B Tech (Chemical, Food, Cosmetics) with minimum 3 to 7 years of experience as QA head in cosmetics/ FMCG industry 1. Quality System Oversight o Develop, implement, and maintain GMP (Good Manufacturing Practices) and ISO standards for cosmetics production.... 

0-2 year experience in Medical Device/Pharma industry. Job Responsibility - Monitoring of qualification and validation activities. - Preparation of technical files and related documentation. - Preparation and review of qualification & validation protocols and reports...

 ...Location: Umargaon/Sarigam, Gujarat — candidates from the Umbergaon–Sarigam–Vapi–Daman–Valsad belt strongly preferred Department: Quality Control (QC) Reports to: Plant Head / Director Experience: 3–6 years of hands-on QC experience in sheet metal, stainless steel... 

 ...Achievement ~ Daily Output Monitoring & Reporting ~ Basic Knowledge of GMP/CGMP ~ SOP Compliance & Production Documentation ~ Quality Control & Rejection Monitoring ~ Machine Troubleshooting & Downtime Monitoring ~5S, Housekeeping & Safety Compliance ~... 

 ...Assist in mechanical engineering, production, manufacturing, maintenance, or quality-related activities. Read and understand mechanical drawings, specifications, and technical documents. Monitor machines, equipment, and production processes. Support installation,... 

 ...clinical evidence discussions during conformity assessment. Work cross-functionally with Regulatory Affairs, Medical Affairs, R&D, Quality, Biostatistics, Risk Management, PMS/Vigilance, Clinical Operations and external consultants/CROs Requirements · Master’s...