Posted by on December 16, 19102 at 03:24:03:
Qualification:
B.Pharm / M.Pharm
Experience :
Minimum 7 Years of experience in performing various activities of Quality Assurance department in pharmaceutical industry. Preference will be given to Candidates with experience of working in all the three dosage forms of LVP (Large volume paranterals ), Oral Solid dosage forms & Oral Liquid Dosage forms
Job Responsibilities :
Field self-inspection of the factory's facilities to ensure and confirm that the manufacturing processes are conducted in accordance with the GMP, GLP and SOP's regulations.
Improve and upgrade manufacturing processes, quality control procedures, maintenance systems and storing functions.
Following up and conducting a periodical training for the personnel on the SOP's to improve and evaluate their performance.
Ensure the implementation of the periodical calibration and validation of the machineries, equipments and processes utilized in different departments related to manufacturing and quality control activities.
Ensure the implementation of the periodical review of the documentation, SOP's records
Inspection of hygiene systems and reviewing the SOP's to ensure high implementation of these SOP's.
Investigating new means to upgrade manufacturing processes in order to improve the quality of products and the productivity of each process.