ScovaiJobsM
Meril
Senior Officer QA
Pardi, INבמשרדקבעמשרה מלאה
פורסם 16 באוק׳ 2026
המשרה פורסמה ב־EN
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.
- Review of raw data, including analytical reports, BMRs, job cards, batch release certificates, data mapping reports, etc.
- Support validation activities across multiple manufacturing segments
Requirements
Qualification & Validation (IQ/OQ/PQ)
Technical Documentation & Technical File Preparation
Protocol and Report Preparation & Review
Data Review & Documentation Verification
GMP Compliance & Regulatory Documentation
Batch Manufacturing Records (BMR) & Analytical Report Review
Cross-functional Coordination & Validation Support
תצלום תפקיד
סוג משרה
משרה מלאה
כישורים נדרשים
Qualification and Validation (IQ/OQ/PQ)Qualification and Validation Activity MonitoringTechnical File PreparationTechnical Documentation PreparationValidation Protocol Preparation and ReviewValidation Report Preparation and ReviewRaw Data Review and Documentation VerificationGMP Compliance and Regulatory DocumentationBatch Manufacturing Record (BMR) ReviewAnalytical Report ReviewCross-functional Coordination and Validation Support
משרות דומות
M
Engineer
Meril
Pardi, INבמשרדקבעמשרה מלאה
אתמול
M
Officer / Sr. Officer
Meril
Pardi, INבמשרדקבעמשרה מלאה
לפני 3 ימים
M
Junior Executive QA
Meril
Pardi, INבמשרדקבעמשרה מלאה
לפני 5 ימים
M
Junior Officer
Meril
Pardi, INבמשרדקבעמשרה מלאה
לפני 5 ימים
M
Clinical Evaluation
Meril
Pardi, INבמשרדקבעמשרה מלאה
לפני 5 ימים
M
Officer
Meril
Pardi, INבמשרדקבעמשרה מלאה
לפני 6 ימים