Ipqa executive

Company Description Eugia Pharma Specialities Ltd (Arabundio) is a growing pharmaceutical organization focused on delivering high-quality, reliable medicines to patients and healthcare providers. The company emphasizes strict adherence to regulatory standards, quality management systems, and continuous improvement across all manufacturing operations. Eugia Pharma fosters a culture of safety, integrity, and collaboration, encouraging team members to contribute ideas that enhance product quality and operational efficiency. Applicants can expect a professional environment that values skill development, compliance, and long-term career growth within the pharmaceutical industry.
Role Description The IPQA Executive role at Eugia Pharma Specialities Ltd (Arabundio) is a full-time, on-site position based in Cuddapah. The IPQA Executive will monitor in-process quality checks during manufacturing and packaging, ensuring compliance with standard operating procedures, batch manufacturing records, and regulatory requirements. This role includes line clearance, in-process sampling, review and approval of in-process documents, and immediate reporting and documentation of deviations or non-conformities. The IPQA Executive will collaborate closely with production, quality control, and regulatory teams to support investigations, implement corrective and preventive actions, and maintain data integrity. The position also involves participation in internal audits, training on quality-related procedures, and supporting continuous improvement initiatives to strengthen overall product quality.
Qualifications
Solid understanding of in-process quality assurance, GMP, and pharmaceutical manufacturing processes.
Experience with documentation practices, batch record review, deviation handling, and CAPA implementation.
Knowledge of regulatory and compliance requirements relevant to pharmaceutical production and packaging.
Strong analytical and problem-solving skills, with attention to detail and data integrity.
Effective communication and collaboration abilities to work with cross-functional teams on-site.
Ability to work in a shift-based manufacturing environment and manage multiple tasks under time constraints.
Diploma or bachelor’s degree in Pharmacy, Chemistry, or a related scientific discipline; prior IPQA or QA experience in pharma is preferred.
Familiarity with audit processes, quality risk management, and continuous improvement methodologies is an advantage.

Work arrangement
No