Executive-qa
5 days ago
From 4 to 9 year(s) of experience
₹ Not Disclosed by Recruiter
- North Goa,Goa
- Preparation and Execution of Equipment Qualification protocols and Reports.
- Involved in execution of CSV and software Validation. Execution in GxP environment
- Document review of URS, FAT, SAT, DQ, IQ, OQ and PQ.
- Preparation & Review of Quality risk management.
- Preparation and Execution of HVAC Qualification and experience in PLC, Validation
- Preparation and Execution of Facility Qualification Protocols and Reports.
- To prepare and update the Validation Master Plan and its annexures.
- Planning of validation activities as per validation master plan to maintain all equipment in validated state within time line.
- Preparation and Execution of Compressed Air Qualification.
- Preparation and Execution of Nitrogen System.
- Preparation and Execution of Temperature Mapping Protocols and Reports.
- Preparation of cleaning validation protocol & Preparation of New product assessment.
- To prepare and update the Cleaning Validation Master Plan and its annexures.
- Successfully attended & being a part of regular audit plan for USFDA, WHO, MHRA.
- Understanding of FDA regulation/ global health care regulation for pharma, regulatory compliance, EU guideline, GAMP 5.
Key Skills
- ValidationOQplcIQPharma
- equipment qualificationProcess ValidationGMPEquipment ValidationUtilityEquipmentQMSVendor Qualification
- Skills highlighted with ‘‘ are preferred keyskills
Education
- UG:_Any Graduate
**Company Profile**:
NMS Consultant
Leading Pharmaceutical Company
- Company Info
**Salary**:
Not Disclosed by Recruiter
Industry:
Pharmaceutical & Life Sciences
Department:
Quality Assurance
Role Category:
Production & Manufacturing
Role:
QA / QC Executive
Employment Type:
Full Time, Permanent
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