● Conduct in-process quality control checks during various stages of pharmaceutical manufacturing to ensure compliance with established standards and specifications.
● Monitor and document critical process parameters, ensuring adherence to Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs).
● Perform sampling, testing, and inspection of raw materials, intermediates, and finished products on the production floor.
● Identify and report deviations, non-conformities, or process anomalies to relevant departments for corrective action.
● Collaborate closely with production, quality assurance, and laboratory teams to resolve quality-related issues promptly.
● Support validation and qualification activities for new processes, equipment, and products.
● Participate in internal audits and contribute to continuous improvement initiatives within the quality control function.
● Bachelor’s degree in Pharmacy, Chemistry, or a related scientific discipline.● 1-3 years of experience in in-process control or quality control within the pharmaceutical industry.● Familiarity with GMP, SOPs, and regulatory requirements for pharmaceutical manufacturing.