Promea Therapeutics
Website:
promea.in
Job details:
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.
- 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.
- 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.
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