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Posted 3 weeks ago |
Job Title: QC Analysts
Activities
- 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.
- 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).
- Ensure that all laboratory equipment is properly calibrated and maintained according to established protocols.
- Assist in troubleshooting equipment issues and coordinating repairs as necessary.
- Stay updated on industry regulations and guidelines to ensure compliance in all testing procedures.
- Participate in internal audits and inspections by regulatory agencies.
- 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.
Candidate Profile
- 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.
- 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.
Application Instructions:
The application deadline is 28th October 2024. Therefore qualified and interested candidates should send their CV to: [email protected] using the Job Title as the subject of the mail.
Job Features
Job Category | Analyst/ Quality Control |