QMS Officer / Executive Production

Preparation and review of SOPs, BMR/BPR.

To process Change control and Deviations.

Proficient in handling Track wise

To initiate Change Control, CAPA, Deviation, Risk assessment, Market complaint, Investigation

To update and maintain Index of SOPs and Formats.

To issue & Retrieve Logbooks, Formats etc.

To assist in compliance for internal and external audits

On line training module knowledge.

Should have good knowledge & proficiency in Computer. Must have worked in QMS of reputed Pharmaceutical industry

Awareness of internal and external audit dealing is required

Regulatory plant experience