QC Analysts at HR Leverage Africa

HR Leverage Africa delivers an excellent spectrum of HR Business Solutions and strategic management support services through a custom-built approach for organizations. As a premium professional HR Boutique firm domiciled in Africa, with our global partners, we leverage on technology in providing one-stop human resources services to various industries in terms of Staffing, Outsourcing, Executive search and recruitment, HR advisory, HR4SMEs, Expatriate management.

We are recruiting to fill the position below:

Job Title: QC Analyst

Location: Sagamu, Ogun
Employment Type: Full-time

Job Summary

• The QC Analyst is responsible for ensuring that all pharmaceutical products meet the required quality standards before they are released for distribution.
• This role involves conducting various tests and analyses on raw materials, in-process samples, and finished products to ensure compliance with regulatory standards and company specifications.

Key Responsibilities
Testing and Analysis:

• Conduct routine and non-routine testing of raw materials, intermediates, and finished products using established analytical methods.
• Perform stability testing and evaluate results to ensure product quality over time.

Documentation:

• Maintain accurate records of all testing procedures, results, and observations in compliance with Good Manufacturing Practices (GMP) and regulatory requirements.
• Prepare and review Quality Control documentation, including test reports and standard operating procedures (SOPs).

Equipment Calibration and Maintenance:

• Ensure that all laboratory equipment is properly calibrated and maintained according to established protocols.
• Assist in troubleshooting equipment issues and coordinating repairs as necessary.

Regulatory Compliance:

• Stay updated on industry regulations and guidelines to ensure compliance in all testing procedures.
• Participate in internal audits and inspections by regulatory agencies.

Collaboration:

• Work closely with cross-functional teams, including production, quality assurance, and research and development, to address quality issues and implement corrective actions.
• Provide technical support during investigations of out-of-specification (OOS) results.

Qualifications

• Education:Bachelor’s Degree in Chemistry, Pharmaceutical Sciences or a related field.
• Experience: Previous experience in a quality control laboratory within the pharmaceutical industry is preferred.
• Skills:
  • Strong analytical skills with proficiency in laboratory techniques (e.g., HPLC, GC, UV-Vis spectroscopy).
  • Excellent attention to detail and organizational skills.
  • Ability to work independently as well as part of a team.
  • Proficient in using laboratory information management systems (LIMS) and Microsoft Office Suite.

Working Conditions

• The position may require working in a laboratory environment with exposure to chemicals and biological materials. Personal protective equipment (PPE) must be worn at all times.

Application Closing Date
28th October, 2024.

Method of Application
Interested and qualified candidates should send their Applications to: [email protected] using the Job Title as the subject of the mail.