QC Analyst

Key Responsibilities

• Perform routine and non-routine analysis of pharmaceutical finished products, and stability samples using HPLC, GC, Dissolution, and other analytical techniques
• Ensure all testing is carried out in compliance with GMP, SOPs, and regulatory requirements
• Accurately document all analytical data, observations, and deviations in accordance with ALCOA+ principles
• Perform equipment calibration, qualification, and routine maintenance as required
• Troubleshoot analytical methods and instruments, and escalate issues when necessary
• Assist in method development and method transfer activities where applicable
• Support laboratory investigations, OOS, and deviation reports with technical input
• Provide support and guidance to junior analysts and contribute to their technical development
• Maintain lab cleanliness, safety, and regulatory compliance at all times

Occasional Duties

• Perform routine analysis of finished products for physical parameters, including: Average Weight, Uniformity of Weight, Disintegration, Friability, Hardness, Water content by Karl Fischer (KF),Identification tests (chemical, UV, IR),Loss on Drying (LOD), and product Description

Candidate Requirements

Minimum Qualifications & Experience:

• A relevant science degree (e.g., Chemistry, Pharmaceutical Sciences, Biochemistry, etc.)
• Minimum of 6 years of experience in a GMP-regulated pharmaceutical testing laboratory
• Strong hands-on experience with HPLC, GC, and Dissolution is essential

Essential Skills:

• Sound understanding of analytical chemistry principles and GMP compliance
• Familiarity with analytical instruments and software (e.g., Empower, Chromeleon)
• Good organizational, communication, and problem-solving skills
• Ability to work independently and collaboratively in a fast-paced environment.