Prepare Review and Maintain SOPs (Standard Operating Procedures) Validation Protocols Batch Records and Other Quality Documents. Ensure Compliance With cGMP FDA MHRA WHO and Other Regulatory Guidelines. Conduct Document Control Activities Including Version Control Issuance Retrieval and Archiving. Support Internal and External Audits By Providing Required Documentation. Assist in Equipment Qualification (IQ OQ PQ) and Validation Processes. Coordinate With The QA/QC Team to Impleme
Experience
1 - 5 Years
No. of Openings
2
Education
Diploma, B.Pharma, B.Sc, B.E, B.Tech
Role
Quality Assurance Quality Control Engineer
Industry Type
Manufacturing / Production / Quality
Gender
Male
Job Country
India
Type of Job
Full Time
Work Location Type
Work from Office
Face interview location
plot no 47, krishna industrial park, sanjan umbergaon road,
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