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 @ Stelis Biopharma
Walk in Time: 9:00 AM to 12:00 PM
Date: 25th November 2023, Saturday
Venue:
Arco Lab Private Limited
19/2, SKR Towers, 15th Cross Rd,
Dollar Layout, 4th Phase, J.P. Nagar,
Bengaluru, Karnataka 560078
Work Location: Stelis Biopharma, Unit 2 Doddaballapur
Contact Person: Dev Kiran 1 9900545421 | [email protected]
1. Department: Quality Control
- 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
2. Department: DP (Drug Product) Manufacturing
- 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
3. Department: DS (Drug Substance) Manufacturing
- Key Skills: DS Manufacturing (Upstream and Downstream)
- Exp: 2 to 8 years
- Should have work experience in Biologics 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.
- Good communication and writing skills
- Seed development in single use bioreactor and carrying out the in process checks
