Job Description

• Bachelor’s degree in Pharmacy, Chemistry, or a related Science discipline.
• Minimum 3–6 years of relevant experience in pharmaceutical Quality Control.
• Strong technical knowledge and hands-on experience in HPLC, GC, UV-Vis spectrophotometry, dissolution testing, and other pharmaceutical analytical techniques.
• Sound knowledge of GMP, GLP, SOPs, and applicable regulatory guidelines, including USP, EP, and BP.
• Experience in analytical method validation, method transfer, and assay analysis.
• Strong understanding of data integrity principles, ALCOA+ compliance, and Good Documentation Practices.
• Working knowledge of Quality Management System activities, including CAPA, AMS, Change Controls, and audit compliance.
• Proficiency in SAP, AmpleLogic, and computer software applications.
• Ability to maintain accurate laboratory records, analytical results, and test reports.
• Strong analytical, troubleshooting, and problem-solving skills.
• Excellent attention to detail and commitment to quality and regulatory compliance.
• Effective written and verbal communication skills.
• Ability to work collaboratively with cross-functional teams, including QA, Production, and R&D.
• Strong organizational and time-management skills with the ability to manage multiple tasks and priorities.
• Highly disciplined, accountable, and responsible, with a strong sense of ownership.
• Self-motivated, adaptable, and willing to learn and implement new technical knowledge.
• Strong commitment to laboratory safety, environmental protection, and continuous improvement.