Walk in interview for M.Pharm, M.Sc as Associate/ Senior Associate at STELIS Biopharma

STELIS Biopharma Pvt. Ltd. is a fully-owned subsidiary of Strides set up in 2013 to consolidate and augment the R&D activities of Inbiopro, which was fully acquired in 2012; and in extending the value chain to manufacturing and commercialisation of the product pipeline. STELIS is pursuing a blended strategy of- developing both ‘biosimilars’ and ‘novel biotherapeutics’ to a ‘Regulated’ market (US/EU) standard for global markets. Our strategy is to offer high-quality bio-pharmaceuticals at affordable prices initially in high-growth Emerging Markets whose vast patient populations offer un-paralleled opportunities for expanded access.

Drug Product fill finish (Manufacturing)
Post : Associate/ Senior Associate
Qualification : B.Pharm/M.Pharm/M. Sc/ B.Tech/M.Tech- Biotechnology. Biochemical / BE - Chemical Engineering
Experience : 3-7 years
Key Skills :
1) Experience in Aseptic processing; Dispensing .formulation,filling
2) C&Q, IQ ,OQ, PQ of commissioning, operation of filling machines (Vial, PFS. cartridge).
3)Experience in operation of isolator
4) Experience in operation of Lycphiliser
5) CGMP and audit knowledge
6) Have experience in managing the compliance requirements (Deviations. Change control, investigations. CAPA). preparat ion of SOPs and protocols for sterile manufacturing
7) Operation of autoclave, dry heat steriliser. Glassware washer, area clean ng and maintenance of dean rooms
8) Validation of equipment area end medis fill

Formulation incharge
Post : Associate/ Senior Associate
Qualification : B.Pharm/M.Pharm/M. Sc/ B.Tech/M.Tech- Biotechnology. Biochemical / BE - Chemical Engineering
Experience : 3-7 years
Key Skills :
1) Experience in Aseptic processing; Dispensing .formulation,filling
2) C&Q, IQ ,OQ, PQ of commissioning, operation of filling machines (Vial, PFS. cartridge).
3)Experience in operation of isolator
4) Experience in operation of Lycphiliser
5) CGMP and audit knowledge
6) Have experience in managing the compliance requirements (Deviations. Change control, investigations. CAPA). preparat ion of SOPs and protocols for sterile manufacturing
7) Operation of autoclave, dry heat steriliser. Glassware washer, area clean ng and maintenance of dean rooms
8) Validation of equipment area end medis fill