- 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.
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.