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

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

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

Job Category: pharma
Job Type: Full Time
Job Location: Doddaballapur - Karnataka

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About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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