Walk-in for Stelis Biopharma on 27th October 2018

Job Posted on Oct 25, 2018

Job Type:	Walk-in
Recruiter Type:	Company
Company Name:	Stelis Biopharma
Interview Venue:	Stelis Biopharma Plot Number 2- D1, Obadenahalli, Doddaballapura 3rd Phase, KIADB Industrial Area., Doddaballapura Taluk, Bangalore Rural. Bangalore India
Contact Person:	Jason
Phone:	9611890198
Email Address:	jason.a@stelis.com
Required in:	Formulation & API both
Job Department(s):	Production
Job Details:	Walk-In Interview at BANGALORE for STELIS BIOPHARMA (Job Location Bangalore - Doddaballapura) Date : Saturday 27th October 2018 1)Associate/ Sr. Associate - DS Manufacturing - Downstream Candidate In Time : 9:00 AM to 12:30 PM *Hands on experience of Chromatography, TFF, Viral filtration skills. * Performing the FAT & SAT at Vendor sites and at our facility respectively. *Performing the IQ, OQ, PQ related to Downstream processing Equipment in Drug substance facility. * Prepare & review of all SOP`s/Protocols related to Equipment facility. * Handling commercial and clinical manufacturing activities of Drug substance facility 2)Associate/Sr. Associate- DS Manufacturing - Upstream *Responsible for Monitoring and operation of Fermenters, Bioreactors , Harvest Vessel Media Preparation vessels, Single use Systems, Kill tanks and other Process Equipment's. * Responsible for Preparation of cell bank, Seed development for the manufacturing batch process. *Involving in the Preventive maintenance of the Process equipment's from time to time. *Responsible for identifying the Problems and Troubleshooting of the same during upstream process execution. 3)Associate/Sr. Associate - DP Manufactruing *Hands on experience of Filling machine. * Isolator operation knowledge. * Performing the IQ, OQ, PQ related to Equipment in Drug product facility. * Prepare & review of all SOP`s/Protocols related to Equipment and Drug product facility. * Hands on experience implementing Good Manufacturing practice in the drug product suite knowledge of US GMP compliance regulations and industry practices, as well as EU GMP. * Assisting in the validation of equipment and facility.
Regulatory Exposure:	Required
Audit Experience:	USFDA, MHRA, WHO
Experience:	2-6 years
Vacancies:	10
Interview Date:	27th October 2018

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