Assistant Manager - Quality Control Nitika Pharmaceuticals
Nitika Pharmaceuticals
Office Location
Full Time
Experience: 3 - 3 years required
Pay:
Salary Information not included
Type: Full Time
Location: Maharashtra
Skills: Quality Control, Documentation, Calibration, GLP, Visual Inspection, Reporting, Incident investigation, Lab cleanliness, Testing procedures, Analytical analysis, Preparation of solutions, QC records maintenance, Training program attendance, Safety reporting
About Nitika Pharmaceuticals
Job Description
1. Following the QC laid down procedures with compliance. 2. Ensure that lab cleanliness and safety standards are maintained 3. Perform the tests as per testing procedures and ensure that all tests are performed according to established item specifications, standard test methods, or protocols. 4. Complete documentation needed to support testing procedures including data capture forms, equipment logbooks, or inventory forms. 5. Calibrate, validate, or maintain laboratory equipment. 6. Review all the laboratory analytical documents, protocol, investigations and lab instrument logs. 7. Following the GLP 8. Conduct routine and non-routine analyses of in-process materials, raw materials, R&D samples, finished products, and stability samples. 9. Preparation of volumetric solutions and reagents 10. Perform visual inspections of finished products. 11. Maintaining QC records, preparing reports and composes correspondence relative to the work. 12. Reporting and investigation of Incident, OOS, OOT and deviation. 13. Attending the training program for QC-SOPs and another relevant SOPs. Ensuring and Reporting safety in work activities in work environment. Job Type: Full-time Schedule: Rotational shift Experience: total work: 3 years (Required) Work Location: In person,