HRLeverage Africa is an HR, Outsourcing and Recruitment Service Provider. As a company, we deliver excellent spectrum of HR Business Solutions through a custom-built approach for organizations. We are a premium professional service firm domiciled in Africa and with our partnership with global organizations, we are able to leverage on technology to provide strategic Business solution.Job Summary
The QC Analyst will be responsible for performing routine and non-routine analysis of raw materials, in-process samples, finished products, and stability samples.
This role ensures that all products meet the established standards of quality, purity, and efficacy.
Key Responsibilities
Sample Analysis:
Conduct chemical and physical analysis of raw materials, in-process samples, finished products, and stability samples using techniques such as HPLC, GC, UV-Vis, FTIR, and titration.
Perform microbiological testing where applicable.
Documentation:
Maintain accurate and detailed records of all analytical results.
Ensure proper documentation of all test results in accordance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
Prepare and review standard operating procedures (SOPs) and test methods.
Equipment Maintenance:
Calibrate, validate, and maintain laboratory equipment to ensure proper functioning.
Troubleshoot and resolve issues with laboratory instruments.
Compliance:
Adhere to all safety, health, and environmental regulations.
Ensure compliance with internal and external quality standards, including FDA, WHO, and other regulatory requirements.
Participate in internal and external audits.
Continuous Improvement:
Identify areas for process improvement within the QC laboratory.
Implement and document changes to enhance quality control processes.
Team Collaboration:
Work closely with production, quality assurance, and research and development teams to ensure product quality.
Provide technical support and training to other laboratory staff.
Reporting:
Prepare and present analytical reports and data summaries to management.
Communicate any deviations or non-conformances observed during analysis.
Qualifications
Education: Bachelor’s Degree in Chemistry, Biochemistry, Pharmacy, or a related field.
Experience: At least 2-3 years of experience in a quality control laboratory in the pharmaceutical industry.
Technical Skills: Proficiency in analytical techniques such as HPLC, GC, UV-Vis, and FTIR. Knowledge of GMP, GLP, and regulatory requirements.
Soft Skills: Excellent attention to detail, strong problem-solving skills, effective communication, and ability to work independently and as part of a team.
Additional Requirements:
Ability to work in a fast-paced environment and manage multiple tasks simultaneously.
Strong organizational skills
Strong organizational skills and ability to maintain accurate records.
Willingness to work flexible hours, including weekends and holidays if necessary.
