Key Responsibilities

• Assist in preparation, review, and control of SOPs, formats, and documents
• Maintain and update QA documentation, records, and logbooks
• Support in implementation of GMP and quality systems
• Assist in handling deviations, change control, and CAPA documentation
• Coordinate with QC, production, and other departments for compliance
• Support internal audits and ensure documentation readiness
• Ensure adherence to quality standards and procedures
• Maintain proper filing and document control system

Must-Have Skills (Non-Negotiable)

• Basic understanding of Quality Assurance concepts and processes
• Strong documentation and record-keeping skills
• High attention to detail and accuracy
• Basic knowledge of GMP and compliance requirements
• Good written and verbal communication skills
• Willingness to learn and follow SOPs strictly
• Disciplined and process-oriented approach

Good-to-Have Skills (Preferred)

• Internship or exposure in QA / documentation
• Basic knowledge of SOPs, CAPA, deviations, and change control
• Awareness of audit processes (internal/external)
• Background in chemical/pharma/manufacturing industry
• Basic computer skills (Excel, Word, documentation handling)
• Analytical thinking and problem-solving approach

What We’re Looking For

• Detail-oriented and compliance-focused individual
• Strong discipline and documentation mindset
• Willingness to build a career in Quality Assurance
• Ability to work in a structured and process-driven environment