Executive Quality Control

Responsibilities

• Perform chemical and instrumental analysis of stability samples and finished products within a hormone block production environment
• Conduct timely charging and withdrawal of samples from stability chambers and maintain accurate documentation
• Calibrate routine laboratory instruments including balances, pH meters, and conductivity meters
• Manage sample reconciliation and maintain destruction records for stability samples
• Implement and adhere to GLP and GMP requirements and procedures
• Utilize LIMS software for sample charging, withdrawal, reconciliation, and data entry
• Evaluate analysis results against SOPs and report any abnormalities to supervisors
• Coordinate practices and procedures in alignment with COBC requirements

Requirements

• B.Pharm or M.Sc. degree
• 2-4 years of experience in Quality Control focusing on chemical and instrumental analysis of finished goods and stability
• Expertise in chemical and instrumental analysis
• Strong knowledge of CAPA and GMP documentation
• Experience with LIMS software
• Exposure to regulatory audits such as MHRA or USFDA

Preferred Qualifications

• Licensed approved chemist

About the Company

Abbott is a global healthcare leader that has been helping people reach their potential for more than 135 years. With a network serving customers in over 160 countries, Abbott creates innovative solutions across diagnostics, medical devices, nutrition, and pharmaceuticals to help people live their best lives through better health.