Executive/Officer Validation & Qualification

FDC; South Goa District; On-site; INR 600,000 - 900,000; Full time

Job summary

FDC Limited, Goa Unit III, is seeking experienced QA professionals to join its Quality Assurance team. The role focuses on IPQA activities, process validation, cleaning validation, and qualification of equipment, facilities, and utilities.

You will review batch records, logbooks, electronic records, and SAP-related quality transactions, ensuring compliance with cGMP and data-integrity requirements. Candidates should have B.Pharm/M.Pharm/M.Sc with relevant experience in pharmaceutical

Qualifications

• B.Pharm/M.Pharm/M.Sc. with relevant experience in a pharmaceutical manufacturing facility.
• Experience in IPQA activities, process validation, cleaning validation and/or qualification.
• Familiarity with SAP and electronic record review.
• Knowledge of GMP, data integrity, and batch documentation.

Responsibilities

• Perform IPQA activities, including sampling and in-process checks during manufacturing and packing.
• Execute and review process validation protocols.
• Prepare validation summary reports.
• Review batch manufacturing/packing records and logbooks.
• Execute and review cleaning validation activities.
• Carry out qualification activities for equipment, facilities and utilities.
• Review electronic records.
• Handle SAP-related quality transactions.
• Maintain documentation in accordance with GMP and regulatory requirements.

Skills

IPQA activities

Process validation

Cleaning validation

Qualification

cGMP knowledge

Data integrity

SAP experience

Education

B.Pharm/M.Pharm/M.Sc. with relevant experience in a pharmaceutical manufacturing facility

Tools

SAP

Job description

We are looking for experienced professionals to join our Quality Assurance team at FDC Limited, Goa Unit III.

Key Responsibilities

• Perform IPQA activities, including sampling and in-process checks during manufacturing and packing
• Execute and review process validation protocols
• Prepare validation summary reports
• Review batch manufacturing/packing records and logbooks
• Execute and review cleaning validation activities
• Carry out qualification activities for equipment, facilities and utilities
• Review electronic records
• Handle SAP-related quality transactions
• Maintain documentation in accordance with GMP and regulatory requirements

Candidate Profile

• B.Pharm/M.Pharm/M.Sc. with relevant experience in a pharmaceutical manufacturing facility
• Practical knowledge of process validation, cleaning validation and/or qualification
• Familiarity with IPQA activities and batch documentation
• Working knowledge of SAP and electronic record review
• Good understanding of cGMP and data-integrity requirements