Executive / Officer - IPQA

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

Job summary

FDC Limited in Goa invites experienced IPQA professionals to join its Quality Assurance team at the pharmaceutical manufacturing facility.

You will perform in-process quality checks, review batch records, ensure GMP compliance, and manage SAP-based quality transactions, while maintaining data integrity and strong documentation and coordination with production and packing teams.

Qualifications

• B.Pharm, M.Pharm or M.Sc. from a recognised institution.
• IPQA experience in a pharmaceutical manufacturing environment.
• Working knowledge of SAP is required.
• Familiarity with batch documentation, electronic records and data-integrity requirements.

Responsibilities

• Perform in-process quality checks, sampling and inspection during manufacturing and packing operations.
• Review batch manufacturing records, batch packing records and equipment logbooks.
• Ensure shop-floor activities comply with current GMP, SOP and regulatory requirements.
• Review electronic records and ensure accuracy, completeness and data integrity.
• Carry out relevant quality transactions in SAP.
• Identify and report deviations and other quality-related observations during manufacturing and packing.
• Coordinate with Production, Packing and other departments to ensure timely compliance and closure of observations.

Skills

IPQA experience

GMP knowledge

Documentation skills

Communication

Coordination

Data integrity

Education

B.Pharm

M.Pharm

M.Sc.

Tools

SAP

Job description

FDC Limited is looking for experienced IPQA professionals to join its Quality Assurance team at its pharmaceutical manufacturing facility in Goa.

Key Responsibilities

• Perform in-process quality checks, sampling and inspection during manufacturing and packing operations.
• Review batch manufacturing records, batch packing records and equipment logbooks.
• Ensure shop-floor activities comply with current GMP, SOP and regulatory requirements.
• Review electronic records and ensure accuracy, completeness and data integrity.
• Carry out relevant quality transactions in SAP.
• Identify and report deviations and other quality-related observations during manufacturing and packing.
• Coordinate with Production, Packing and other departments to ensure timely compliance and closure of observations.

Candidate Requirements

• B.Pharm, M.Pharm or M.Sc. from a recognised institution.
• Relevant IPQA experience in a pharmaceutical manufacturing environment.
• Working knowledge of SAP is required.
• Familiarity with batch documentation, electronic records and data-integrity requirements.
• Sound knowledge of GMP practices and shop-floor quality systems.
• Good documentation, communication and coordination skills.