Job description 1. Implementation and improvement in Quality Management System as per ISO 13485:2016. 2. Implementation & Formation of Standard Operating Procedure (SOP) & Protocols as per GMP. 3. Maintain complete documents of various departments like Site Master File, Device Master File with easy archival/retrieval. 4. Involve onsite into the calibration & Validation activities. Preparation of Calibration calendar and preventive maintenance. 5. Assist in preparation of Batch Manufacturing Record as per manufacturing and their review before release of the batch. 6. Giving line clearance before starting the New Batch. Role: Quality Assurance - Other Industry Type: Medical Services / Hospital (Diagnostics) Department: Quality Assurance Employment Type: Full Time, Permanent Role Category: Quality Assurance - Other Education UG: B.Pharma in Any Specialization, B.Tech/B.E. in Any Specialization PG: Any Postgraduate Doctorate: Doctorate Not Required Key Skills Skills highlighted with ‘‘ are preferred keyskills Quality Assurance preventive maintenanceQuality Assurance ExecutiveQuality ManagementBatch Manufacturing
Job Summary
Company
MACOM
Location
Sonipat
Salary Range
Not disclosed
Experience
2-4 Yrs
Verification
Government Verified Recruiter
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