Key Responsibilities
Implement, maintain, monitor, and continuously improve the Quality Management System.
Ensure compliance with applicable Good Manufacturing Practices (GMP), regulatory requirements, and internal quality procedures.
Prepare, review, revise, and maintain Standard Operating Procedures (SOPs), quality manuals, policies, and other controlled documents.
Coordinate internal audits, external audits, customer audits, and regulatory inspections, as applicable.
Manage deviations, non-conformances, investigations, root cause analysis, and Corrective and Preventive Actions (CAPA).
Oversee document control, change control, training records, and quality-related documentation.
Coordinate with Quality Control (QC), Production, Stores, Engineering, and other departments to address quality issues.
Monitor compliance with approved procedures and ensure timely closure of audit observations and corrective actions.
Support quality risk assessments and periodic reviews of the Quality Management System.
Maintain audit trails, compliance records, and other quality documentation.
Assist in investigating customer complaints and product quality issues, where applicable.
Prepare quality reports and support management reviews and continuous improvement initiatives.
Guide team members on QMS requirements, documentation practices, and quality procedures.
Experience
10 - 15 Years
No. of Openings
1
Education
Post Graduate (M.D.S., MD/Medicine Doctor, M.Pharma, M.Sc)
Role
QMS Manager
Industry Type
Pharma / BioTech / Clinical Research
Gender
[ Male / Female ]
Job Country
India
Type of Job
Full Time
Work Location Type
Work from Office
Face Interview Location
Near Raja Biscuit Chowk , Jasmine Hotel , SIDCUL , Haridwar