Job Description

A Quality Control (QC) Officer in the pharmaceutical industry inspects and tests raw materials, in-process samples, and finished products to ensure they meet quality, safety, and regulatory standards. Key duties include performing analytical tests, documenting all findings, investigating deviations, maintaining equipment, and ensuring compliance with regulations like cGMP and GLP. They are also responsible for maintaining quality-related documentation and collaborating with other departments to resolve quality issues.

Key responsibilities

Testing and analysis:

Conduct analytical testing on raw materials, in-process samples, and finished products using various instruments like HPLC and FTIR.

Quality assurance:

Ensure products comply with established quality standards, regulatory requirements, and pharmacopoeias.

Documentation:

Maintain accurate and detailed records of all testing, results, and investigations in accordance with regulatory requirements.

Equipment maintenance:

Perform calibration and maintenance on laboratory instruments and equipment.

Deviation management:

Investigate and report any deviations or out-of-specification (OOS) results, and implement corrective and preventive actions (CAPA).

Process improvement:

Collaborate with other departments, such as production and R&D, to address quality issues and contribute to continuous improvement of processes.

Regulatory compliance:

Ensure adherence to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).

Reporting:

Prepare Certificates of Analysis (COA), stability summaries, and other quality reports for management and stakeholders.
Job Type: Full-time

Pay: ?15,000.00 - ?20,000.00 per month

Work Location: Remote