Walk in for Quality Control, DP Manufacturing, DS Manufacturing at Stelis Biopharma- on 25th November 2023

Stelis Biopharma

Website Stelis Biopharma

About Stelis Biopharma

Stelis Biopharma operates as a Contract Development and Manufacturing Organization, covering the entire biologics development and production process. The company offers a comprehensive range of services, starting from cell line technology transfer and extending to clinical and commercial manufacturing. Stelis Biopharma demonstrates proven technical expertise in various technology platforms, including microbial, mammalian, viral vectors, and other relevant bioprocessing technologies. Stelis Biopharma is positioned to provide high-quality services for global programs, indicating a broad reach and capability to support clients on an international scale.

Quality Control Department

Key Skills: QC-Analytics

Experience: 2 to 8 years

  • Analysis of raw material, packing material, in-process samples, stability samples, and finished products.
  • Expertise in handling HPLC, GC, UV, IR & KF Titrator.
  • Calibrating analytical equipment as and when required.
  • Ensuring cGLP compliance, data integrity & safety.
  • Good communication and writing skills

DP (Drug Product) Manufacturing Department

Key Skills: DP Manufacturing

Experience Required at Stelis Biopharma: 2 to 8 years

  • Responsible for DP facility manufacturing activities like Compounding, Filtration, Filling, and lyophilization of the Vial line products.
  • Assisting in installation and commissioning activities like FAT, SAT, etc., of the Filling lines for vials, formulation vessels, sterilizers, lyophilizers, ALUs, sealing machines, isolators, etc.
  • Preparation and review of the OQ protocols, CLIA, QRM of all associated equipment and area.
  • Ensuring QMS compliance in manufacturing-related activities.
  • Assisting in the validations of equipment and facility and the process (aseptic media fill).
  • Identifying and implementing manufacturing and warehouse procedures with compliance to current GMP requirements.
  • Good communication and writing skills

DS (Drug Substance) Manufacturing Department

Key Skills: DS Manufacturing (Upstream and Downstream)

Experience Required at Stelis Biopharma: 2 to 8 years

  • Work experience in Biologies DS manufacturing sites.
  • Responsible for executing the day-to-day activities in DS Manufacturing.
  • Executing the IQ, OQ, and PQ of Single-Use Bioreactor and system in DS manufacturing area.
  • Microbial and Mammalian Experience.
  • Bioreactor (mammalian and viral culture), single-use media preparation, single-use manifold, autoclave, filter integrity.
  • Seed development in single-use bioreactor and carrying out the in-process checks.
  • Good communication and writing skills

Work Location:

Stelis Biopharma, Unit 2 Doddaballapur – Karnataka

Walk-in Interview

Date: 25th November 2023, Saturday

Time: 9:00 am to 12:00 pm

Venue: Arco Lab Private Limited, 19/2, SKR Towers, 15th Cross Rd, Dollar Layout, 4th Phase, J.P Nagar, Bengaluru, Karnataka 560078