- Experience: .
- Experience in audits & documentation
- Good analytical,problem-solving,and communication skills
- Testing & Analysis: Perform testing using HPLC, GC, UV, IR, and Dissolution techniques to ensure accuracy and reliability of test results. Maintain consistency in analytical procedures to meet quality standards.
- Quality Monitoring: Ensure quality is maintained across warehouse, dispatch, and packaging activities. Collaborate with operations teams to identify and resolve quality issues in real-time, preventing defects and ensuring compliance.
- Compliance & Documentation: Adhere to cGMP and regulatory guidelines while maintaining accurate documentation of all quality-related activities. Ensure records are up to date and comply with industry standards.
- Deviation & CAPA Management: Investigate deviations and non-conformances, conduct root cause analysis (RCA), and implement corrective and preventive actions (CAPA)
to mitigate risks and enhance process efficiency.
- Audits & Inspections: Participate in internal and external audits, ensuring compliance with regulatory requirements. Assist in preparing responses to audit observations and contribute to continuous improvement initiatives.
- Training & Process Improvement: Provide training to teams on quality standards, best practices, and regulatory updates. Support the development and review of quality procedures to enhance operational efficiency and ensure adherence to the latest industry trends.
Experience:
- Relevant years in Quality Control for speciality industrial chemicals.
- Knowledge of cGMP & regulatory standards.
- Strong skills in deviation investigation, RCA & CAPA. Experience in audits & documentation.
- Positive analytical, problem-solving, and communication skills