Job details: Quality Assurance
Experience: 2 - 6 Years
Role: Quality Assurance– API Manufacturing
Industry: Pharmaceutical (Active Pharmaceutical Ingredients)
QUALITY ASSURANCE JOB DESCRIPTION:
Responsible for release of batches and ensures proper procedures are followed in determining release of a batch.
Responsible for handling of change control deviation CAPA OOS OOT Market complaint Vendor Management system.
To conduct internal audit as per schedule.
To conduct the SOPs GMP GDP & Data integrity training.
Responsible for carrying out investim gation related Deviation OOS OOT Market Complaint.
To monitoring of CAPA & preparation / review of quality trend analysis.
Responsible for preparation / review of Annual Product Quality Review.
Monitoring of control sample as per schedule.
To preparation / review of master documents like Specification SOPs BMR BPR STP Site master file Validation master plan etc.
Continuous improvement of Quality Standards with respect to cGMP requirements.
Responsible for document issuance & review.
Preparation / review of validation qualification protocol & report.
Handling and implementation of Quality Management System with respect to current revision of SOP
Required Skills:
Quality Management Pharma Mining Quality Assurance Visio Manufacturing Internal Audit
Job details: Quality AssuranceExperience: 2 - 6 YearsRole: Quality Assurance– API ManufacturingIndustry: Pharmaceutical (Active Pharmaceutical Ingredients)QUALITY ASSURANCE JOB DESCRIPTION:Responsible for release of batches and ensures proper procedures are followed in determining release of a batch...
Job details: Quality Assurance
Experience: 2 - 6 Years
Role: Quality Assurance– API Manufacturing
Industry: Pharmaceutical (Active Pharmaceutical Ingredients)
QUALITY ASSURANCE JOB DESCRIPTION:
Responsible for release of batches and ensures proper procedures are followed in determining release of a batch.
Responsible for handling of change control deviation CAPA OOS OOT Market complaint Vendor Management system.
To conduct internal audit as per schedule.
To conduct the SOPs GMP GDP & Data integrity training.
Responsible for carrying out investim gation related Deviation OOS OOT Market Complaint.
To monitoring of CAPA & preparation / review of quality trend analysis.
Responsible for preparation / review of Annual Product Quality Review.
Monitoring of control sample as per schedule.
To preparation / review of master documents like Specification SOPs BMR BPR STP Site master file Validation master plan etc.
Continuous improvement of Quality Standards with respect to cGMP requirements.
Responsible for document issuance & review.
Preparation / review of validation qualification protocol & report.
Handling and implementation of Quality Management System with respect to current revision of SOP
Required Skills:
Quality Management Pharma Mining Quality Assurance Visio Manufacturing Internal Audit
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