Responsible for Media preparation, media stock, Media consumption record & Related Documentation.
Responsible for Growth promotion test of rehydrated media.
Responsible for Daily record of lab and equipment & instrument.
Responsible for Daily PH Meter & balance calibration.
Responsible for Preparation / Review of SOP, validation protocol & Report etc.
Responsible for Environmental monitoring of clean room and other controlled area.
Responsible for Water sampling and testing.
Responsible for MLT Test of RM, FP, Bulk, Packing material as per pharmacopeia / specification.
Responsible for Sterility test, BET Test, media Fill, BIs test as per specification.
Responsible for Master sub culturing and record.
Responsible for Validation / calibration of lab equipment & instrument.
Responsible for Area validation and qualification.
Responsible for Validation of autoclave, Incubators & Dry heat sterilizer.
Responsible for Online Documentation with respect to GLP, GDP, GMP.
Responsible for taking initiative of Change control, OOS, Deviation, CAPA etc.
Responsible for keep update and of analyzed reports / Analytical data sheets, formats, log books, records, specifications for raw material, packaging material, finished products and test methods to ensure compliance with statutory and company standards.
Responsible for analysis stability analysis and review of documents.
Responsible for follow good laboratory Practices.

Responsible for ensuring that all necessary testing is carried out as well as stability studies and quality review.
Responsible for calibration of instruments / Equipments.
Responsible for checking the maintenance of the department, premises and equipment.
Responsible for ensuring that the records are made manually and/or by recording instruments to demonstrate that all the required sampling, inspection and testing procedures were actually carried out. Any deviations are fully recorded.
Responsible for ensuring that the records which are made of the results of inspection and testing of materials, intermediates, bulk and finished products are formally assessed against specification.
Responsible for actual sampling and testing procedures and the actual sampling and testing of starting materials, intermediate products and finished products to verify that they meet the specifications before release for further manufacture.
Any other assignment allocated by the Department head or designee.

More Jobs at Zenzi Pharmaceutical Industries

Assistant Manager-Quality Control

murbad

12.0 - 15.0 yrs

INR 8 - 10 Lacs

Injectable Production Officer

murbad

4.0 - 5.0 yrs

INR 4 - 5 Lacs

Purchase Executive

dombivli, kalyan

7.0 - 8.0 yrs

INR 5 - 6 Lacs

Microbiologist-Executive

murbad

7.0 - 8.0 yrs

INR 6 - 7 Lacs

Mock Interview

Practice Video Interview with JobPe AI

Start Job-Specific Interview

Start Your Job Search Today

Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.