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.
Quality Control Department
Key Skills : QC-Analytics
Exp : 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.
• To ensure cGLP compliance. Data integrity & safety.
Good communication and writing skills
DP (Drug Product) Manufacturing Department
Key Skills : DP Manufacturing
Exp : 2 to 8 years
• 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 fill).
• Identify and implement the 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)
Exp : 2 to 8 years
• Should have 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
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