Job Responsibilities
- Planning and managing, day to day analysis of received samples. Ensuring on time release of received samples for the products in Quality control dept. and Microbiology dept.
- 2. Conduct routine and non-routine analyses of in-process materials, raw materials, packing materials, finished goods or stability samples for In-vitro Diagnostic, Large volume parentals, and Cyto-biologics manufacturing products.
- 3. Devising, improving, and reviewing new specifications and procedures for products or processes, and training staff to use them.
- Perform the quality inspection process of new part samples and record the data.
- Interpret test results, compare them to established specifications and control limits, and make recommendation on appropriate ness of data release.
- Investigate customer complaints regarding quality issues and develop a solution.
- Record, compile, and prepare report for analysis and evaluation.
- Observing and complying with GxP's, GLP, GMP and GDP.
- Assist in auditing, writing, revising, and verifying quality standard and developing forms and instruction for recording and reporting quality data.
- Monitoring performance of quality control system to ensure effectiveness and efficiency.
- Participate in the development of product specifications and analytical Method validation of products.
Skills Required
Gxp, analytical method validation , Gmp, Glp