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
Contact Person:Jason
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
Interview Date:27th October 2018

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