About the Company
Sun pharma is an Indian manufacturing pharmaceutical company with more than 40 manufacturing sites and more than 100 countries serving markets with more than 30000 employees and 2000 marketed products.
The company established in 1983 with 2-person marketing team and in 1994 launched and IPO. In 1991 it established an process development R & D center primarily. Now it has more than 2000 scientists.
The products include anti retrovirals, OTC drugs, API (Active pharmaceutical substances) urology, nephrology and so on
About the job
Executive production
Location of the job - Bangalore
Candidate need to have good understanding on process scale up and technology transfer activity
Strong knowledge and experience in depth filtration nominal filtration and filtration activities
Need to have good manufacturing practise documentation Give MS activity like change controls and deviations
Need to be well versed with the upstream fermentation centrifugation homogenization filtration and upstream process
Need to have experience and knowledge on SIPCIP mixing vessels and auto cleaving process
Need to be open for working in shift operations and meet to solve the problems that were erased in the shop floor during the manufacturing process
For packing manufacturing assistant
Location of the job : Mohali
Candidate need to maintain the equipment hygiene areas and sanitary conditions and required to fill the BPR and supporting documents and records
Candidate need to follow the governing procedures and standard operating procedures and maintain good personal hygiene during the entry of the production area
Candidate me to get the records verified by the supervisor at the end of the shift or after the batch completion process
Need to have strong knowledge on tapping machine of secondary packing bottle packing literature pasting machine print and inspection cartoner machine
Need to have idea on LMS
Senior officer in quality control
Location of the job : Mohali
Candidate need to prepare the SAP COA and regulatory COA as per the guidance of local procedures and requirement
Candidate need to Perform the laboratory activity as assigned by the supervisor or the lab in charge
Need to have strong understanding of OOT, OOS and deviations in track wise software
Need to document and maintain the precise records and accurate should document as per the contemporaries policy
Able to handle the testing of stability samples finished products and raw materials
Required to follow the laboratory procedures and maintain the complaints EHS policies in line to see GMP recruitment
Required to update the working standards and calibration activity qualification of lab instruments preventive maintenance as and when required
Required to maintain the registers log books and perform the analytical method transfer activities