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Job Description
- Conduct quality control tests on raw materials, in-process samples, and finished pharmaceutical products.
- Ensure compliance with Good Manufacturing Practices (GMP) and regulatory standards.
- Collaborate with production and R&D teams to establish and maintain quality control protocols.
- Investigate and resolve quality issues through root cause analysis and corrective actions.
- Maintain detailed and accurate documentation of quality control procedures, test results, and compliance reports.
- Perform audits of manufacturing processes to ensure adherence to quality standards.
- Stay updated on regulatory requirements and ensure that processes align with industry guidelines.
- Provide training to staff on quality control procedures and best practices.
Job Requirements
- Strong understanding of Good Manufacturing Practices (GMP) and regulatory compliance (FDA, EMA, etc.).
- Experience with analytical techniques such as HPLC, GC, and UV spectrophotometry.
- Excellent attention to detail and problem-solving skills.
- Strong documentation skills and experience maintaining quality control records.
- Good communication skills and the ability to work collaboratively in cross-functional teams.
- Knowledge of pharmaceutical production processes and laboratory procedures.
- Experience in performing internal audits and addressing quality issues.
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