ProPharma Group seeks a Quality Specialist to support GxP compliance and quality management activities across pharmaceutical and biotech programs. The role involves managing deviations, quality events, and corrective actions, plus supporting client audits and regulatory inspections.

Responsibilities

Maintain GxP compliance and support eQMS activities including Change Control and CAPAs

Develop, review, and approve Deviations and Quality Events; communicate root cause analysis

Coordinate audit and inspection preparations, manage CAPA responses, and track closure

Perform effectiveness checks on Deviations and Quality Events to assess CAPA efficacy

Collect, analyze, and report on quality data related to CAPAs, Deviations, and KPIs

Requirements

Bachelor's degree and/or minimum 2 years of Quality Assurance experience

Fluent English speaking and writing skills

Knowledge of GxP Quality Management Systems and eQMS platforms

Proficiency with Microsoft Office Suite (Outlook, Word, Excel, PowerPoint)

Experience handling Deviations, Quality Events, CAPAs, and Effectiveness Checks

Solid organizational, prioritization, and project management abilities

Excellent written and interpersonal communication skills

📌 Quality Officer - Biotechnology (India)
🏢 Propharma Group
📍 India