QUALITY CONTROL OFFICER – Lopsymed Pharmaceuticals 1478 views

Key Responsibilities

• Create and update QC procedures, inspection criteria, and documentation.
• Oversee all stages of production (incoming materials, in-process, final inspection). Accurately document all test data and results in compliance with cGMP and company SOPs (Standard Operating Procedures).
• Define sampling plans and statistical process control (SPC) methods.
• Manage the calibration and maintenance of testing equipment.
• Participate in investigations for out-of-specification (OOS) and out-of-trend (OOT) results.
• Calibrate, operate, and maintain laboratory equipment, ensuring it is in a validated state.
• Review and verify analytical data and documentation generated by colleagues.
• Support the stability testing program by preparing and testing stability samples according to predefined protocols.
• Ensure the Quality Control and laboratory is maintained in a clean, safe, and inspection-ready state at all times.
• Collaborate closely with Quality Assurance (QA), Manufacturing, and warehouse departments to resolve quality issues and drive continuous improvement.
• Participate in GMP and other audits and implement corrective and preventive actions (CAPA).

Requirements

• Certificate/Diploma in Laboratory Sciences.
• Working knowledge of cGMP and pharmaceutical quality systems.
• Self-motivated, with the ability to work proactively using own initiative.
• Committed to learning and development.
• Microsoft Office (Word, Excel and Outlook
• Good communication and teamwork skills.

How to Apply