Stelis Biopharma – Walk-In Interviews on 3rd Dec’ 2023 for Multiple Positions

Stelis Biopharma (A Strides Enterprise), We are a fully integrated pure-play biologics Contract Development and Manufacturing Organization (CDMO), offering the complete spectrum of services, from cell line technology transfer to clinical and commercial manufacturing with capabilities to convert drug substance into stable formulations and fill and finish formats. We have proven technical expertise in microbial, mammalian, viral vectors, and various other technology platforms with world-class cGMP manufacturing facilities that offer high-quality services for your global programs.

Walk-In Drive for Stelis Biopharma

Departments: DP Manufacturing

• Experience: 2 to 8 years
• Work Location: Stelis – Unit 2, Doddaballapur, Bangalore

Key responsibilities:

• Responsible for DP facility manufacturing activities like Compounding, Filtration, Filling and lyophilization of the Vial line products.
• Assist the installation and commissioning activities like FAT, SAT etc. of the Filling lines for vials, formulation vessels, Sterilisers, Lyophilizers, ALUS, Sealing Machine, Isolator etc.
• Preparation and review of the OQ protocols, CLIA, QRM of all associated equipment and area.
• Ensure QMS compliance in manufacturing related activities.
• Assist the validations of equipment and facility and the process (aseptic media fil).
• Identify and implement the manufacturing and warehouse procedures with compliance to current GMP requirements.
• Good communication and writing skills.

Departments: DP Packing

• Experience: 2 to 8 years
• Work Location: Stelis Unit 2, Doddaballapur, Bangalore

Key responsibilities:

• Should have the knowledge and hand experience on handling of Packaging line with diversity of products packaging.
• Should have the knowledge and hands on experience with Labelling machines, Blister packing machine, Automatic Cartoning Machine, Pen Assembling machines.
• Should have the knowledge and hands on experience with Track and trace system and aggregation system.
• Should have the knowledge and hands on experience with Preparation and review of the URS, QRM, IQ, OQ and PQ protocols.
• Should have the basic knowledge of handling the Cold chain products.