Quality Control Officer at HRLeverage Africa

Key Responsibilities

Testing and Analysis:

• Conduct routine and non-routine testing of raw materials, in-process samples, and finished pharmaceutical products.
• Perform analytical tests, including but not limited to HPLC, UV-Vis spectroscopy, titration, and microbial analysis.
• Ensure compliance with established quality standards, specifications, and Good Laboratory Practices (GLP).

Documentation and Reporting:

• Accurately document all testing procedures, results, and deviations.
• Prepare and submit comprehensive reports on testing outcomes to the Quality Control Manager.
• Maintain records in compliance with regulatory requirements (e.g., FDA, WHO, NAFDAC).

Compliance and Regulatory Standards:

• Ensure adherence to pharmaceutical quality standards such as GMP, GLP, and ICH guidelines.
• Participate in internal and external audits, including regulatory inspections, as required.
• Implement corrective and preventive actions (CAPAs) for identified quality issues.

Equipment and Instrumentation:

• Calibrate, maintain, and troubleshoot laboratory equipment to ensure optimal performance.
• Verify the functionality of laboratory instruments and address malfunctions promptly.
• Maintain an inventory of laboratory supplies and ensure the availability of necessary reagents.

Collaboration and Coordination:

• Work closely with production, QA, and R&D teams to resolve quality-related issues.
• Support investigations into non-conforming products or deviations from standard procedures.
• Assist in the development and validation of new testing methods and procedures.

Training and Development:

• Participate in training programs to stay updated on new quality control techniques and regulatory changes.
• Provide guidance to junior laboratory staff or interns as needed.

Qualifications

Education:

• Bachelor's Degree in Chemistry, Biochemistry, Microbiology, Pharmacy, or a related field.

Experience:

• Minimum of 2–3 years of experience in quality control within a pharmaceutical manufacturing environment.
• Proficiency in laboratory techniques and use of analytical instruments.

Skills and Competencies:

• Strong attention to detail and analytical skills.
• Good understanding of pharmaceutical regulatory requirements (e.g., GMP, GLP, and ICH guidelines).
• Excellent documentation and record-keeping abilities.
• Proficiency in Microsoft Office Suite and laboratory data management systems.
• Strong communication and teamwork skills.

Work Environment:

• Laboratory setting with potential exposure to chemicals and biohazards.
• May require working flexible hours, including weekends, to meet production timelines